共 26 条
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CLOVES Syndrome in a Nine-month-old Infant
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Alomar, Sara
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CUREUS JOURNAL OF MEDICAL SCIENCE,
2019, 11 (09)

Alomar, Sara
论文数: 0 引用数: 0
h-index: 0
机构:
Alfaisal Univ, Coll Med, Riyadh, Saudi Arabia Alfaisal Univ, Coll Med, Riyadh, Saudi Arabia

Khedr, Rewana E.
论文数: 0 引用数: 0
h-index: 0
机构:
Alfaisal Univ, Coll Med, Riyadh, Saudi Arabia Alfaisal Univ, Coll Med, Riyadh, Saudi Arabia

Alajlan, Saad
论文数: 0 引用数: 0
h-index: 0
机构:
King Faisal Specialist Hosp & Res Ctr, Dermatol, Riyadh, Saudi Arabia Alfaisal Univ, Coll Med, Riyadh, Saudi Arabia
[2]
Characterization of a distinct syndrome that associates complex truncal overgrowth, vascular, and acral anomalies: a descriptive study of 18 cases of CLOVES syndrome
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Alomari, Ahmad I.
.
CLINICAL DYSMORPHOLOGY,
2009, 18 (01)
:1-7

Alomari, Ahmad I.
论文数: 0 引用数: 0
h-index: 0
机构:
Childrens Hosp Boston, Dept Radiol, Div Vasc & Intervent Radiol, Boston, MA 02115 USA
Harvard Univ, Sch Med, Boston, MA USA Childrens Hosp Boston, Dept Radiol, Div Vasc & Intervent Radiol, Boston, MA 02115 USA
[3]
Overgrowth syndromes: is dysfunctional PI3-kinase signalling a unifying mechanism?
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Barker, KT
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Houlston, RS
.
EUROPEAN JOURNAL OF HUMAN GENETICS,
2003, 11 (09)
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Barker, KT
论文数: 0 引用数: 0
h-index: 0
机构:
Inst Canc Res, Sect Canc Genet, Sutton SM2 5NG, Surrey, England Inst Canc Res, Sect Canc Genet, Sutton SM2 5NG, Surrey, England

Houlston, RS
论文数: 0 引用数: 0
h-index: 0
机构:
Inst Canc Res, Sect Canc Genet, Sutton SM2 5NG, Surrey, England Inst Canc Res, Sect Canc Genet, Sutton SM2 5NG, Surrey, England
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Barrett D, 2012, PEDIATR DRUGS, V14, P299, DOI 10.2165/11594740-000000000-00000
[5]
PI3K Signaling in Tissue Hyper-Proliferation: From Overgrowth Syndromes to Kidney Cysts
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De Santis, Maria Chiara
;
Sala, Valentina
;
Martini, Miriam
;
Ferrero, Giovanni Battista
;
Hirsch, Emilio
.
CANCERS,
2017, 9 (04)

De Santis, Maria Chiara
论文数: 0 引用数: 0
h-index: 0
机构:
Univ Torino, Dept Mol Biotechnol & Hlth Sci, I-10126 Turin, Italy Univ Torino, Dept Mol Biotechnol & Hlth Sci, I-10126 Turin, Italy

Sala, Valentina
论文数: 0 引用数: 0
h-index: 0
机构:
Univ Torino, Dept Mol Biotechnol & Hlth Sci, I-10126 Turin, Italy Univ Torino, Dept Mol Biotechnol & Hlth Sci, I-10126 Turin, Italy

Martini, Miriam
论文数: 0 引用数: 0
h-index: 0
机构:
Univ Torino, Dept Mol Biotechnol & Hlth Sci, I-10126 Turin, Italy Univ Torino, Dept Mol Biotechnol & Hlth Sci, I-10126 Turin, Italy

Ferrero, Giovanni Battista
论文数: 0 引用数: 0
h-index: 0
机构:
Univ Torino, Dept Publ Hlth & Pediat, I-10126 Turin, Italy Univ Torino, Dept Mol Biotechnol & Hlth Sci, I-10126 Turin, Italy

Hirsch, Emilio
论文数: 0 引用数: 0
h-index: 0
机构:
Univ Torino, Dept Mol Biotechnol & Hlth Sci, I-10126 Turin, Italy Univ Torino, Dept Mol Biotechnol & Hlth Sci, I-10126 Turin, Italy
[6]
Gopal Balaji, 2015, Indian J Radiol Imaging, V25, P71, DOI 10.4103/0971-3026.150166
[7]
Utility of clinical high-depth next generation sequencing for somatic variant detection in the PIK3CA-related overgrowth spectrum
[J].
Hucthagowder, V.
;
Shenoy, A.
;
Corliss, M.
;
Vigh-Conrad, K. A.
;
Storer, C.
;
Grange, D. K.
;
Cottrell, C. E.
.
CLINICAL GENETICS,
2017, 91 (01)
:79-85

Hucthagowder, V.
论文数: 0 引用数: 0
h-index: 0
机构:
Washington Univ, Sch Med, Dept Pathol & Immunol, St Louis, MO USA Washington Univ, Sch Med, Dept Pathol & Immunol, St Louis, MO USA

Shenoy, A.
论文数: 0 引用数: 0
h-index: 0
机构:
Washington Univ, Sch Med, Dept Pathol & Immunol, St Louis, MO USA Washington Univ, Sch Med, Dept Pathol & Immunol, St Louis, MO USA

Corliss, M.
论文数: 0 引用数: 0
h-index: 0
机构:
Washington Univ, Sch Med, Dept Pathol & Immunol, St Louis, MO USA Washington Univ, Sch Med, Dept Pathol & Immunol, St Louis, MO USA

Vigh-Conrad, K. A.
论文数: 0 引用数: 0
h-index: 0
机构:
Washington Univ, Sch Med, Dept Genet, St Louis, MO USA Washington Univ, Sch Med, Dept Pathol & Immunol, St Louis, MO USA

论文数: 引用数:
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机构:

Grange, D. K.
论文数: 0 引用数: 0
h-index: 0
机构:
Washington Univ, Sch Med, Div Genet & Genom Med, Dept Pediat, St Louis, MO USA Washington Univ, Sch Med, Dept Pathol & Immunol, St Louis, MO USA

Cottrell, C. E.
论文数: 0 引用数: 0
h-index: 0
机构:
Washington Univ, Sch Med, Dept Pathol & Immunol, St Louis, MO USA
Washington Univ, Sch Med, Dept Genet, St Louis, MO USA Washington Univ, Sch Med, Dept Pathol & Immunol, St Louis, MO USA
[8]
PIK3CA-Related Overgrowth Spectrum (PROS): Diagnostic and Testing Eligibility Criteria, Differential Diagnosis, and Evaluation
[J].
Keppler-Noreuil, Kim M.
;
Rios, Jonathan J.
;
Parker, Victoria E. R.
;
Semple, Robert K.
;
Lindhurst, Marjorie J.
;
Sapp, Julie C.
;
Alomari, Ahmad
;
Ezaki, Marybeth
;
Dobyns, William
;
Biesecker, Leslie G.
.
AMERICAN JOURNAL OF MEDICAL GENETICS PART A,
2015, 167 (02)
:287-295

Keppler-Noreuil, Kim M.
论文数: 0 引用数: 0
h-index: 0
机构:
NHGRI, NIH, Bethesda, MD 20892 USA NHGRI, NIH, Bethesda, MD 20892 USA

Rios, Jonathan J.
论文数: 0 引用数: 0
h-index: 0
机构:
Univ Texas SW Med Ctr Dallas, Sarah M & Charles E Seay Ctr Musculoskeletal Res, Eugene McDermott Ctr Human Growth & Dev, Texas Scottish Rite Hosp Children,Dept Pediat, Dallas, TX 75390 USA
Univ Texas SW Med Ctr Dallas, Dept Orthopaed Surg, Dallas, TX 75390 USA NHGRI, NIH, Bethesda, MD 20892 USA

Parker, Victoria E. R.
论文数: 0 引用数: 0
h-index: 0
机构:
Univ Cambridge, Metab Res Labs, Inst Metab Sci, Cambridge, MA USA NHGRI, NIH, Bethesda, MD 20892 USA

Semple, Robert K.
论文数: 0 引用数: 0
h-index: 0
机构:
Univ Cambridge, Metab Res Labs, Inst Metab Sci, Cambridge, MA USA NHGRI, NIH, Bethesda, MD 20892 USA

Lindhurst, Marjorie J.
论文数: 0 引用数: 0
h-index: 0
机构:
NHGRI, NIH, Bethesda, MD 20892 USA NHGRI, NIH, Bethesda, MD 20892 USA

Sapp, Julie C.
论文数: 0 引用数: 0
h-index: 0
机构:
NHGRI, NIH, Bethesda, MD 20892 USA NHGRI, NIH, Bethesda, MD 20892 USA

Alomari, Ahmad
论文数: 0 引用数: 0
h-index: 0
机构:
Boston Childrens Hosp, Div Vasc & Intervent Radiol, Boston, MA USA
Harvard Univ, Sch Med, Boston, MA USA NHGRI, NIH, Bethesda, MD 20892 USA

Ezaki, Marybeth
论文数: 0 引用数: 0
h-index: 0
机构:
Univ Texas SW Med Ctr Dallas, Dept Orthopaed Surg, Dallas, TX 75390 USA NHGRI, NIH, Bethesda, MD 20892 USA

Dobyns, William
论文数: 0 引用数: 0
h-index: 0
机构:
Univ Washington, Seattle, WA 98195 USA NHGRI, NIH, Bethesda, MD 20892 USA

Biesecker, Leslie G.
论文数: 0 引用数: 0
h-index: 0
机构:
NHGRI, NIH, Bethesda, MD 20892 USA NHGRI, NIH, Bethesda, MD 20892 USA
[9]
Clinical delineation and natural history of the PIK3CA-related overgrowth spectrum
[J].
Keppler-Noreuil, Kim M.
;
Sapp, Julie C.
;
Lindhurst, Marjorie J.
;
Parker, Victoria E. R.
;
Blumhorst, Cathy
;
Darling, Thomas
;
Tosi, Laura L.
;
Huson, Susan M.
;
Whitehouse, Richard W.
;
Jakkula, Eveliina
;
Grant, Ian
;
Balasubramanian, Meena
;
Chandler, Kate E.
;
Fraser, Jamie L.
;
Gucev, Zoran
;
Crow, Yanick J.
;
Brennan, Leslie Manace
;
Clark, Robin
;
Sellars, Elizabeth A.
;
Pena, Loren D. M.
;
Krishnamurty, Vidya
;
Shuen, Andrew
;
Braverman, Nancy
;
Cunningham, Michael L.
;
Sutton, V. Reid
;
Tasic, Velibor
;
Graham, John M., Jr.
;
Geer, Joseph, Jr.
;
Henderson, Alex
;
Semple, Robert K.
;
Biesecker, Leslie G.
.
AMERICAN JOURNAL OF MEDICAL GENETICS PART A,
2014, 164 (07)
:1713-1733

Keppler-Noreuil, Kim M.
论文数: 0 引用数: 0
h-index: 0
机构:
NHGRI, NIH, Bethesda, MD 20892 USA NHGRI, NIH, Bethesda, MD 20892 USA

Sapp, Julie C.
论文数: 0 引用数: 0
h-index: 0
机构:
NHGRI, NIH, Bethesda, MD 20892 USA NHGRI, NIH, Bethesda, MD 20892 USA

Lindhurst, Marjorie J.
论文数: 0 引用数: 0
h-index: 0
机构:
NHGRI, NIH, Bethesda, MD 20892 USA NHGRI, NIH, Bethesda, MD 20892 USA

Parker, Victoria E. R.
论文数: 0 引用数: 0
h-index: 0
机构:
Univ Cambridge, Metab Res Labs, Inst Metab Sci, Cambridge, England NHGRI, NIH, Bethesda, MD 20892 USA

Blumhorst, Cathy
论文数: 0 引用数: 0
h-index: 0
机构:
NHGRI, NIH, Bethesda, MD 20892 USA NHGRI, NIH, Bethesda, MD 20892 USA

Darling, Thomas
论文数: 0 引用数: 0
h-index: 0
机构:
Uniformed Serv Univ Hlth Sci, Dept Dermatol, Bethesda, MD 20814 USA NHGRI, NIH, Bethesda, MD 20892 USA

Tosi, Laura L.
论文数: 0 引用数: 0
h-index: 0
机构:
Childrens Natl Med Ctr, Div Orthopaed Surg & Sports Med, Washington, DC 20010 USA NHGRI, NIH, Bethesda, MD 20892 USA

Huson, Susan M.
论文数: 0 引用数: 0
h-index: 0
机构:
Univ Manchester, Cent Manchester Univ Hosp NHS Fdn Trust, Inst Human Dev,Fac Med & Human Sci, Manchester Ctr Genom Med,MAHSC, Manchester, Lancs, England NHGRI, NIH, Bethesda, MD 20892 USA

Whitehouse, Richard W.
论文数: 0 引用数: 0
h-index: 0
机构:
Manchester Royal Infirm, Cent Manchester Univ Hosp NHS Fdn Trust, Dept Radiol, Manchester M13 9WL, Lancs, England NHGRI, NIH, Bethesda, MD 20892 USA

Jakkula, Eveliina
论文数: 0 引用数: 0
h-index: 0
机构:
Univ Helsinki, Cent Hosp, Dept Clin Genet, Helsinki, Finland NHGRI, NIH, Bethesda, MD 20892 USA

Grant, Ian
论文数: 0 引用数: 0
h-index: 0
机构:
Cambridge Univ Hosp NHS Trust, Dept Plast Surg, Cambridge, England NHGRI, NIH, Bethesda, MD 20892 USA

Balasubramanian, Meena
论文数: 0 引用数: 0
h-index: 0
机构:
Sheffield Childrens NHS Fdn Trust, Sheffield Clin Genet Serv, Sheffield, S Yorkshire, England NHGRI, NIH, Bethesda, MD 20892 USA

Chandler, Kate E.
论文数: 0 引用数: 0
h-index: 0
机构:
Univ Manchester, Cent Manchester Univ Hosp NHS Fdn Trust, Inst Human Dev,Fac Med & Human Sci, Manchester Ctr Genom Med,MAHSC, Manchester, Lancs, England NHGRI, NIH, Bethesda, MD 20892 USA

Fraser, Jamie L.
论文数: 0 引用数: 0
h-index: 0
机构:
NHGRI, NIH, Bethesda, MD 20892 USA NHGRI, NIH, Bethesda, MD 20892 USA

Gucev, Zoran
论文数: 0 引用数: 0
h-index: 0
机构:
Univ Skopje, Dept Endocrinol & Genet, Skopje, North Macedonia NHGRI, NIH, Bethesda, MD 20892 USA

Crow, Yanick J.
论文数: 0 引用数: 0
h-index: 0
机构:
Univ Manchester, Cent Manchester Univ Hosp NHS Fdn Trust, Inst Human Dev,Fac Med & Human Sci, Manchester Ctr Genom Med,MAHSC, Manchester, Lancs, England NHGRI, NIH, Bethesda, MD 20892 USA

Brennan, Leslie Manace
论文数: 0 引用数: 0
h-index: 0
机构:
Univ Calif San Francisco, Kaiser Permanente Oakland, San Francisco, CA 94143 USA NHGRI, NIH, Bethesda, MD 20892 USA

Clark, Robin
论文数: 0 引用数: 0
h-index: 0
机构:
Loma Linda Univ, Dept Pediat, Med Ctr, Div Med Genet, Loma Linda, CA 92350 USA NHGRI, NIH, Bethesda, MD 20892 USA

Sellars, Elizabeth A.
论文数: 0 引用数: 0
h-index: 0
机构:
Arkansas Childrens Hosp, Sect Genet & Metab, Little Rock, AR 72202 USA NHGRI, NIH, Bethesda, MD 20892 USA

Pena, Loren D. M.
论文数: 0 引用数: 0
h-index: 0
机构:
Duke Univ, Med Ctr, Dept Pediat, Div Genet, Durham, NC 27710 USA NHGRI, NIH, Bethesda, MD 20892 USA

Krishnamurty, Vidya
论文数: 0 引用数: 0
h-index: 0
机构:
Pediat Clin, Alpharetta, GA USA
Genet Clin, Alpharetta, GA USA NHGRI, NIH, Bethesda, MD 20892 USA

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Braverman, Nancy
论文数: 0 引用数: 0
h-index: 0
机构:
McGill Univ, Montreal Childrens Hosp, Res Inst, Dept Human Genet & Pediat, Montreal, PQ H3H 1P3, Canada NHGRI, NIH, Bethesda, MD 20892 USA

Cunningham, Michael L.
论文数: 0 引用数: 0
h-index: 0
机构:
Univ Washington, Sch Med, Div Craniofacial Med, Seattle, WA USA NHGRI, NIH, Bethesda, MD 20892 USA

Sutton, V. Reid
论文数: 0 引用数: 0
h-index: 0
机构:
Baylor Coll Med, Dept Mol & Human Genet, Houston, TX 77030 USA NHGRI, NIH, Bethesda, MD 20892 USA

Tasic, Velibor
论文数: 0 引用数: 0
h-index: 0
机构:
Univ Childrens Hosp, Sch Med, Skopje, North Macedonia NHGRI, NIH, Bethesda, MD 20892 USA

Graham, John M., Jr.
论文数: 0 引用数: 0
h-index: 0
机构:
Harbor UCLA Med Ctr, Dept Pediat, Los Angeles, CA USA NHGRI, NIH, Bethesda, MD 20892 USA

Geer, Joseph, Jr.
论文数: 0 引用数: 0
h-index: 0
机构:
Greenwood Genet Ctr, Greenwood, SC 29646 USA NHGRI, NIH, Bethesda, MD 20892 USA

Henderson, Alex
论文数: 0 引用数: 0
h-index: 0
机构:
Newcastle Upon Tyne Hosp, Northern Genet Serv, Newcastle Upon Tyne, Tyne & Wear, England NHGRI, NIH, Bethesda, MD 20892 USA

Semple, Robert K.
论文数: 0 引用数: 0
h-index: 0
机构:
Univ Cambridge, Metab Res Labs, Inst Metab Sci, Cambridge, England NHGRI, NIH, Bethesda, MD 20892 USA

Biesecker, Leslie G.
论文数: 0 引用数: 0
h-index: 0
机构:
NHGRI, NIH, Bethesda, MD 20892 USA NHGRI, NIH, Bethesda, MD 20892 USA
[10]
Molecular diagnosis of PIK3CA-related overgrowth spectrum (PROS) in 162 patients and recommendations for genetic testing
[J].
Kuentz, Paul
;
St-Onge, Judith
;
Duffourd, Yannis
;
Courcet, Jean-Benoit
;
Carmignac, Virginie
;
Jouan, Thibaud
;
Sorlin, Arthur
;
Abasq-Thomas, Claire
;
Albuisson, Juliette
;
Amiel, Jeanne
;
Amram, Daniel
;
Arpin, Stephanie
;
Attie-Bitach, Tania
;
Bahi-Buisson, Nadia
;
Barbarot, Sebastien
;
Baujat, Genevieve
;
Bessis, Didier
;
Boccara, Olivia
;
Bonniere, Maryse
;
Boute, Odile
;
Bursztejn, Anne-Claire
;
Chiaverini, Christine
;
Cormier-Daire, Valerie
;
Coubes, Christine
;
Delobel, Bruno
;
Edery, Patrick
;
El Chehadeh, Salima
;
Francannet, Christine
;
Genevieve, David
;
Goldenberg, Alice
;
Haye, Damien
;
Isidor, Bertrand
;
Jacquemont, Marie-Line
;
Van Kien, Philippe Khau
;
Lacombe, Didier
;
Martin, Ludovic
;
Martinovic, Jelena
;
Maruani, Annabel
;
Mathieu-Dramard, Michele
;
Mazereeuw-Hautier, Juliette
;
Michot, Caroline
;
Mignot, Cyril
;
Miquel, Juliette
;
Morice-Picard, Fanny
;
Petit, Florence
;
Phan, Alice
;
Rossi, Massimiliano
;
Touraine, Renaud
;
Verloes, Alain
;
Vincent, Marie
.
GENETICS IN MEDICINE,
2017, 19 (09)
:989-997

Kuentz, Paul
论文数: 0 引用数: 0
h-index: 0
机构:
CHU Dijon Bourgogne, Federat Hosp Univ Med Translat & Anomalies Dev, Dijon, France
Univ Bourgogne Franche Comte, Genet Anomalies Dev, Equipe Accueil 4271, Dijon, France
CHRU Besancon, Genet Biol Histol, Besancon, France CHU Dijon Bourgogne, Federat Hosp Univ Med Translat & Anomalies Dev, Dijon, France

St-Onge, Judith
论文数: 0 引用数: 0
h-index: 0
机构:
CHU Dijon Bourgogne, Federat Hosp Univ Med Translat & Anomalies Dev, Dijon, France
Univ Bourgogne Franche Comte, Genet Anomalies Dev, Equipe Accueil 4271, Dijon, France
McGill Univ, Ctr Hlth, Res Inst, Child Hlth & Human Dev Program, Montreal, PQ, Canada CHU Dijon Bourgogne, Federat Hosp Univ Med Translat & Anomalies Dev, Dijon, France

Duffourd, Yannis
论文数: 0 引用数: 0
h-index: 0
机构:
CHU Dijon Bourgogne, Federat Hosp Univ Med Translat & Anomalies Dev, Dijon, France
Univ Bourgogne Franche Comte, Genet Anomalies Dev, Equipe Accueil 4271, Dijon, France CHU Dijon Bourgogne, Federat Hosp Univ Med Translat & Anomalies Dev, Dijon, France

Courcet, Jean-Benoit
论文数: 0 引用数: 0
h-index: 0
机构:
Univ Bourgogne Franche Comte, Genet Anomalies Dev, Equipe Accueil 4271, Dijon, France
CHU Dijon Bourgogne, Serv Pediat & Genet Med 1, Dijon, France CHU Dijon Bourgogne, Federat Hosp Univ Med Translat & Anomalies Dev, Dijon, France

Carmignac, Virginie
论文数: 0 引用数: 0
h-index: 0
机构:
CHU Dijon Bourgogne, Federat Hosp Univ Med Translat & Anomalies Dev, Dijon, France
Univ Bourgogne Franche Comte, Genet Anomalies Dev, Equipe Accueil 4271, Dijon, France CHU Dijon Bourgogne, Federat Hosp Univ Med Translat & Anomalies Dev, Dijon, France

Jouan, Thibaud
论文数: 0 引用数: 0
h-index: 0
机构:
CHU Dijon Bourgogne, Federat Hosp Univ Med Translat & Anomalies Dev, Dijon, France
Univ Bourgogne Franche Comte, Genet Anomalies Dev, Equipe Accueil 4271, Dijon, France CHU Dijon Bourgogne, Federat Hosp Univ Med Translat & Anomalies Dev, Dijon, France

Sorlin, Arthur
论文数: 0 引用数: 0
h-index: 0
机构:
CHU Dijon Bourgogne, Federat Hosp Univ Med Translat & Anomalies Dev, Dijon, France
Univ Bourgogne Franche Comte, Genet Anomalies Dev, Equipe Accueil 4271, Dijon, France CHU Dijon Bourgogne, Federat Hosp Univ Med Translat & Anomalies Dev, Dijon, France

Abasq-Thomas, Claire
论文数: 0 引用数: 0
h-index: 0
机构:
CHU Brest Morvan, Dept Pediat & Genet Med, Brest, France CHU Dijon Bourgogne, Federat Hosp Univ Med Translat & Anomalies Dev, Dijon, France

Albuisson, Juliette
论文数: 0 引用数: 0
h-index: 0
机构:
Hop Europeen Georges Pompidou, Ctr Reference Malad Vasc Rares, Paris, France CHU Dijon Bourgogne, Federat Hosp Univ Med Translat & Anomalies Dev, Dijon, France

Amiel, Jeanne
论文数: 0 引用数: 0
h-index: 0
机构:
Hop Necker Enfants Malad, Serv Genet Med, Paris, France CHU Dijon Bourgogne, Federat Hosp Univ Med Translat & Anomalies Dev, Dijon, France

Amram, Daniel
论文数: 0 引用数: 0
h-index: 0
机构:
CHI Creteil, Unite Genet Clin, Creteil, France CHU Dijon Bourgogne, Federat Hosp Univ Med Translat & Anomalies Dev, Dijon, France

Arpin, Stephanie
论文数: 0 引用数: 0
h-index: 0
机构:
CHRU Tours, Serv Genet Clin, Tours, France CHU Dijon Bourgogne, Federat Hosp Univ Med Translat & Anomalies Dev, Dijon, France

Attie-Bitach, Tania
论文数: 0 引用数: 0
h-index: 0
机构:
Hop Necker Enfants Malad, Serv Histol Embryol Cytogenet, Paris, France CHU Dijon Bourgogne, Federat Hosp Univ Med Translat & Anomalies Dev, Dijon, France

Bahi-Buisson, Nadia
论文数: 0 引用数: 0
h-index: 0
机构:
Hop Necker Enfants Malad, Serv Genet Med, Paris, France CHU Dijon Bourgogne, Federat Hosp Univ Med Translat & Anomalies Dev, Dijon, France

Barbarot, Sebastien
论文数: 0 引用数: 0
h-index: 0
机构:
CHU Nantes, Serv Dermatol, Nantes, France CHU Dijon Bourgogne, Federat Hosp Univ Med Translat & Anomalies Dev, Dijon, France

Baujat, Genevieve
论文数: 0 引用数: 0
h-index: 0
机构:
Hop Necker Enfants Malad, Serv Genet Med, Paris, France CHU Dijon Bourgogne, Federat Hosp Univ Med Translat & Anomalies Dev, Dijon, France

Bessis, Didier
论文数: 0 引用数: 0
h-index: 0
机构:
CHRU Montpellier, Dept Dermatol, Montpellier, France CHU Dijon Bourgogne, Federat Hosp Univ Med Translat & Anomalies Dev, Dijon, France

论文数: 引用数:
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Bonniere, Maryse
论文数: 0 引用数: 0
h-index: 0
机构:
Hop Necker Enfants Malad, Serv Histol Embryol Cytogenet, Paris, France CHU Dijon Bourgogne, Federat Hosp Univ Med Translat & Anomalies Dev, Dijon, France

Boute, Odile
论文数: 0 引用数: 0
h-index: 0
机构:
CHU Lille, Serv Genet Clin, Lille, France CHU Dijon Bourgogne, Federat Hosp Univ Med Translat & Anomalies Dev, Dijon, France

Bursztejn, Anne-Claire
论文数: 0 引用数: 0
h-index: 0
机构:
CHU Nancy, Serv Dermatol, Nancy, France CHU Dijon Bourgogne, Federat Hosp Univ Med Translat & Anomalies Dev, Dijon, France

Chiaverini, Christine
论文数: 0 引用数: 0
h-index: 0
机构:
CHU Nice, Serv Dermatol, Nice, France CHU Dijon Bourgogne, Federat Hosp Univ Med Translat & Anomalies Dev, Dijon, France

Cormier-Daire, Valerie
论文数: 0 引用数: 0
h-index: 0
机构:
Hop Necker Enfants Malad, Serv Genet Med, Paris, France CHU Dijon Bourgogne, Federat Hosp Univ Med Translat & Anomalies Dev, Dijon, France

Coubes, Christine
论文数: 0 引用数: 0
h-index: 0
机构:
CHRU Montpellier, Dept Genet Med Malad Rares & Med Personnalisee, Montpellier, France CHU Dijon Bourgogne, Federat Hosp Univ Med Translat & Anomalies Dev, Dijon, France

Delobel, Bruno
论文数: 0 引用数: 0
h-index: 0
机构:
GH Inst Catholique Lille, Ctr Genet Chromos, Lille, France CHU Dijon Bourgogne, Federat Hosp Univ Med Translat & Anomalies Dev, Dijon, France

Edery, Patrick
论文数: 0 引用数: 0
h-index: 0
机构:
Hosp Civils Lyon, Dept Genet, Lyon, France
Claude Bernard Lyon 1 Univ, Lyon Neurosci Res Ctr, GENDEV Team, INSERM,U1028,CNRS,UMR 5292, Lyon, France CHU Dijon Bourgogne, Federat Hosp Univ Med Translat & Anomalies Dev, Dijon, France

El Chehadeh, Salima
论文数: 0 引用数: 0
h-index: 0
机构:
Hop Hautepierre, Hop Univ Strasbourg, Serv Genet Med, Strasbourg, France CHU Dijon Bourgogne, Federat Hosp Univ Med Translat & Anomalies Dev, Dijon, France

Francannet, Christine
论文数: 0 引用数: 0
h-index: 0
机构:
CHU Clermont Ferrand, Serv Genet Med, Clermont Ferrand, France CHU Dijon Bourgogne, Federat Hosp Univ Med Translat & Anomalies Dev, Dijon, France

Genevieve, David
论文数: 0 引用数: 0
h-index: 0
机构:
CHRU Montpellier, Dept Genet Med Malad Rares & Med Personnalisee, Montpellier, France CHU Dijon Bourgogne, Federat Hosp Univ Med Translat & Anomalies Dev, Dijon, France

Goldenberg, Alice
论文数: 0 引用数: 0
h-index: 0
机构:
CHU Rouen, Serv Genet, Rouen, France
Univ Rouen, Ctr Normand Genom Med & Med Personnalisee, INSERM, U1079, Rouen, France CHU Dijon Bourgogne, Federat Hosp Univ Med Translat & Anomalies Dev, Dijon, France

Haye, Damien
论文数: 0 引用数: 0
h-index: 0
机构:
CHU Tours, Serv Pediat, Tours, France CHU Dijon Bourgogne, Federat Hosp Univ Med Translat & Anomalies Dev, Dijon, France

Isidor, Bertrand
论文数: 0 引用数: 0
h-index: 0
机构:
CHU Nantes, Serv Genet Med, Nantes, France CHU Dijon Bourgogne, Federat Hosp Univ Med Translat & Anomalies Dev, Dijon, France

Jacquemont, Marie-Line
论文数: 0 引用数: 0
h-index: 0
机构:
CHU Reunion, Unite Genet Med, St Pierre, Reunion, France CHU Dijon Bourgogne, Federat Hosp Univ Med Translat & Anomalies Dev, Dijon, France

Van Kien, Philippe Khau
论文数: 0 引用数: 0
h-index: 0
机构:
CHU Nimes, Unite Genet Med & Cytogenet, Nimes, France CHU Dijon Bourgogne, Federat Hosp Univ Med Translat & Anomalies Dev, Dijon, France

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Martin, Ludovic
论文数: 0 引用数: 0
h-index: 0
机构:
CHU Angers, Serv Dermatol, Angers, France CHU Dijon Bourgogne, Federat Hosp Univ Med Translat & Anomalies Dev, Dijon, France

Martinovic, Jelena
论文数: 0 引用数: 0
h-index: 0
机构:
Hop Antoine Beclere, APHP, Unite Foetopathol, Clamart, France CHU Dijon Bourgogne, Federat Hosp Univ Med Translat & Anomalies Dev, Dijon, France

Maruani, Annabel
论文数: 0 引用数: 0
h-index: 0
机构:
Univ Tours, Serv Dermatol, Unite Dermatol Pediat, CIC,Inserm 1415, Tours, France CHU Dijon Bourgogne, Federat Hosp Univ Med Translat & Anomalies Dev, Dijon, France

Mathieu-Dramard, Michele
论文数: 0 引用数: 0
h-index: 0
机构:
CHU Amiens, Ctr Activ Genet Clin & Oncogenet, Amiens, France CHU Dijon Bourgogne, Federat Hosp Univ Med Translat & Anomalies Dev, Dijon, France

Mazereeuw-Hautier, Juliette
论文数: 0 引用数: 0
h-index: 0
机构:
CHU Toulouse, Ctr Reference Malad Rares Peau, Toulouse, France CHU Dijon Bourgogne, Federat Hosp Univ Med Translat & Anomalies Dev, Dijon, France

Michot, Caroline
论文数: 0 引用数: 0
h-index: 0
机构:
Hop Necker Enfants Malad, Serv Genet Med, Paris, France CHU Dijon Bourgogne, Federat Hosp Univ Med Translat & Anomalies Dev, Dijon, France

Mignot, Cyril
论文数: 0 引用数: 0
h-index: 0
机构:
GH La Pitie Salpetriere, APHP,Dept Genet & Cytogenet, Ctr Reference Deficiences Intellectuelles Causes, GRC UPMC Deficiences Intellectuelles & Autisme, Paris, France CHU Dijon Bourgogne, Federat Hosp Univ Med Translat & Anomalies Dev, Dijon, France

Miquel, Juliette
论文数: 0 引用数: 0
h-index: 0
机构:
CHU Reunion, Serv Pediat Gen, St Pierre, Reunion, France CHU Dijon Bourgogne, Federat Hosp Univ Med Translat & Anomalies Dev, Dijon, France

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Petit, Florence
论文数: 0 引用数: 0
h-index: 0
机构:
CHU Lille, Serv Genet Clin, Lille, France CHU Dijon Bourgogne, Federat Hosp Univ Med Translat & Anomalies Dev, Dijon, France

Phan, Alice
论文数: 0 引用数: 0
h-index: 0
机构:
CHU Lyon, Serv Dermatol, Lyon, France CHU Dijon Bourgogne, Federat Hosp Univ Med Translat & Anomalies Dev, Dijon, France

Rossi, Massimiliano
论文数: 0 引用数: 0
h-index: 0
机构:
Hosp Civils Lyon, Dept Genet, Lyon, France
Claude Bernard Lyon 1 Univ, Lyon Neurosci Res Ctr, GENDEV Team, INSERM,U1028,CNRS,UMR 5292, Lyon, France CHU Dijon Bourgogne, Federat Hosp Univ Med Translat & Anomalies Dev, Dijon, France

Touraine, Renaud
论文数: 0 引用数: 0
h-index: 0
机构:
CHU St Etienne, Serv Genet Clin, St Priest En Jarez, France CHU Dijon Bourgogne, Federat Hosp Univ Med Translat & Anomalies Dev, Dijon, France

Verloes, Alain
论文数: 0 引用数: 0
h-index: 0
机构:
Hop Robert Debre, Unite Fonct Genet Clin, Paris, France CHU Dijon Bourgogne, Federat Hosp Univ Med Translat & Anomalies Dev, Dijon, France

Vincent, Marie
论文数: 0 引用数: 0
h-index: 0
机构:
CHU Nantes, Serv Genet Med, Nantes, France CHU Dijon Bourgogne, Federat Hosp Univ Med Translat & Anomalies Dev, Dijon, France