共 293 条
[71]
MATHEMATICAL LEARNING DISABILITIES IN CHILDREN WITH 22Q11.2 DELETION SYNDROME: A REVIEW
[J].
De Smedt, Bert
;
Swillen, Ann
;
Verschaffel, Lieven
;
Ghesquiere, Pol
.
DEVELOPMENTAL DISABILITIES RESEARCH REVIEWS,
2009, 15 (01)
:4-10

De Smedt, Bert
论文数: 0 引用数: 0
h-index: 0
机构:
Katholieke Univ Leuven, Ctr Parenting Child Welf & Disabil, Leuven, Belgium Katholieke Univ Leuven, Ctr Parenting Child Welf & Disabil, Leuven, Belgium

Swillen, Ann
论文数: 0 引用数: 0
h-index: 0
机构:
Katholieke Univ Leuven, Ctr Human Genet, Louvain, Belgium
Katholieke Univ Leuven, Dept Rehabil Sci, Louvain, Belgium Katholieke Univ Leuven, Ctr Parenting Child Welf & Disabil, Leuven, Belgium

Verschaffel, Lieven
论文数: 0 引用数: 0
h-index: 0
机构:
Katholieke Univ Leuven, Ctr Instruct Psychol & Technol, Louvain, Belgium Katholieke Univ Leuven, Ctr Parenting Child Welf & Disabil, Leuven, Belgium

Ghesquiere, Pol
论文数: 0 引用数: 0
h-index: 0
机构:
Katholieke Univ Leuven, Ctr Parenting Child Welf & Disabil, Leuven, Belgium Katholieke Univ Leuven, Ctr Parenting Child Welf & Disabil, Leuven, Belgium
[72]
Disease-associated epigenetic changes in monozygotic twins discordant for schizophrenia and bipolar disorder
[J].
Dempster, Emma L.
;
Pidsley, Ruth
;
Schalkwyk, Leonard C.
;
Owens, Sheena
;
Georgiades, Anna
;
Kane, Fergus
;
Kalidindi, Sridevi
;
Picchioni, Marco
;
Kravariti, Eugenia
;
Toulopoulou, Timothea
;
Murray, Robin M.
;
Mill, Jonathan
.
HUMAN MOLECULAR GENETICS,
2011, 20 (24)
:4786-4796

Dempster, Emma L.
论文数: 0 引用数: 0
h-index: 0
机构:
Kings Coll London, Inst Psychiat, SGDP Ctr, MRC, London SE5 8AF, England Kings Coll London, Inst Psychiat, SGDP Ctr, MRC, London SE5 8AF, England

Pidsley, Ruth
论文数: 0 引用数: 0
h-index: 0
机构:
Kings Coll London, Inst Psychiat, SGDP Ctr, MRC, London SE5 8AF, England Kings Coll London, Inst Psychiat, SGDP Ctr, MRC, London SE5 8AF, England

Schalkwyk, Leonard C.
论文数: 0 引用数: 0
h-index: 0
机构:
Kings Coll London, Inst Psychiat, SGDP Ctr, MRC, London SE5 8AF, England Kings Coll London, Inst Psychiat, SGDP Ctr, MRC, London SE5 8AF, England

Owens, Sheena
论文数: 0 引用数: 0
h-index: 0
机构:
Kings Coll London, Dept Psychosis Studies, London SE5 8AF, England Kings Coll London, Inst Psychiat, SGDP Ctr, MRC, London SE5 8AF, England

Georgiades, Anna
论文数: 0 引用数: 0
h-index: 0
机构:
Kings Coll London, Dept Psychosis Studies, London SE5 8AF, England Kings Coll London, Inst Psychiat, SGDP Ctr, MRC, London SE5 8AF, England

Kane, Fergus
论文数: 0 引用数: 0
h-index: 0
机构:
Kings Coll London, Dept Psychosis Studies, London SE5 8AF, England Kings Coll London, Inst Psychiat, SGDP Ctr, MRC, London SE5 8AF, England

Kalidindi, Sridevi
论文数: 0 引用数: 0
h-index: 0
机构:
Kings Coll London, Dept Psychosis Studies, London SE5 8AF, England Kings Coll London, Inst Psychiat, SGDP Ctr, MRC, London SE5 8AF, England

Picchioni, Marco
论文数: 0 引用数: 0
h-index: 0
机构:
Kings Coll London, Dept Psychosis Studies, London SE5 8AF, England
St Andrews Acad Ctr, Northampton NN1 5BG, England Kings Coll London, Inst Psychiat, SGDP Ctr, MRC, London SE5 8AF, England

Kravariti, Eugenia
论文数: 0 引用数: 0
h-index: 0
机构:
Kings Coll London, Dept Psychosis Studies, London SE5 8AF, England Kings Coll London, Inst Psychiat, SGDP Ctr, MRC, London SE5 8AF, England

Toulopoulou, Timothea
论文数: 0 引用数: 0
h-index: 0
机构:
Kings Coll London, Dept Psychosis Studies, London SE5 8AF, England Kings Coll London, Inst Psychiat, SGDP Ctr, MRC, London SE5 8AF, England

Murray, Robin M.
论文数: 0 引用数: 0
h-index: 0
机构:
Kings Coll London, Dept Psychosis Studies, London SE5 8AF, England Kings Coll London, Inst Psychiat, SGDP Ctr, MRC, London SE5 8AF, England

Mill, Jonathan
论文数: 0 引用数: 0
h-index: 0
机构:
Kings Coll London, Inst Psychiat, SGDP Ctr, MRC, London SE5 8AF, England Kings Coll London, Inst Psychiat, SGDP Ctr, MRC, London SE5 8AF, England
[73]
Familial and sporadic 15q13.3 microdeletions in idiopathic generalized epilepsy: precedent for disorders with complex inheritance
[J].
Dibbens, Leanne M.
;
Mullen, Saul
;
Helbig, Ingo
;
Mefford, Heather C.
;
Bayly, Marta A.
;
Bellows, Susannah
;
Leu, Costin
;
Trucks, Holger
;
Obermeier, Tanja
;
Wittig, Michael
;
Franke, Andre
;
Caglayan, Hande
;
Yapici, Zuhal
;
Sander, Thomas
;
Eichler, Evan E.
;
Scheffer, Ingrid E.
;
Mulley, John C.
;
Berkovic, Samuel F.
.
HUMAN MOLECULAR GENETICS,
2009, 18 (19)
:3626-3631

Dibbens, Leanne M.
论文数: 0 引用数: 0
h-index: 0
机构:
SA Pathol Womens & Childrens Hosp, Epilepsy Res Program, Adelaide, SA 5006, Australia
Univ Adelaide, Sch Paediat & Reprod Hlth, Adelaide, SA 5005, Australia SA Pathol Womens & Childrens Hosp, Epilepsy Res Program, Adelaide, SA 5006, Australia

Mullen, Saul
论文数: 0 引用数: 0
h-index: 0
机构:
Univ Melbourne, Dept Med, Epilepsy Res Ctr, Heidelberg, Vic 3081, Australia SA Pathol Womens & Childrens Hosp, Epilepsy Res Program, Adelaide, SA 5006, Australia

Helbig, Ingo
论文数: 0 引用数: 0
h-index: 0
机构:
Univ Med Ctr Schleswig Holstein, Inst Clin Mol Biol, Dept Neuropediat, D-24105 Kiel, Germany SA Pathol Womens & Childrens Hosp, Epilepsy Res Program, Adelaide, SA 5006, Australia

Mefford, Heather C.
论文数: 0 引用数: 0
h-index: 0
机构:
Univ Washington, Dept Pediat, Seattle, WA 98195 USA
Univ Washington, Dept Genome Sci, Seattle, WA 98195 USA SA Pathol Womens & Childrens Hosp, Epilepsy Res Program, Adelaide, SA 5006, Australia

Bayly, Marta A.
论文数: 0 引用数: 0
h-index: 0
机构:
SA Pathol Womens & Childrens Hosp, Epilepsy Res Program, Adelaide, SA 5006, Australia SA Pathol Womens & Childrens Hosp, Epilepsy Res Program, Adelaide, SA 5006, Australia

Bellows, Susannah
论文数: 0 引用数: 0
h-index: 0
机构:
Univ Melbourne, Dept Med, Epilepsy Res Ctr, Heidelberg, Vic 3081, Australia SA Pathol Womens & Childrens Hosp, Epilepsy Res Program, Adelaide, SA 5006, Australia

Leu, Costin
论文数: 0 引用数: 0
h-index: 0
机构:
Univ Cologne, Cologne Ctr Genom, Cologne, Germany SA Pathol Womens & Childrens Hosp, Epilepsy Res Program, Adelaide, SA 5006, Australia

Trucks, Holger
论文数: 0 引用数: 0
h-index: 0
机构:
Univ Cologne, Cologne Ctr Genom, Cologne, Germany SA Pathol Womens & Childrens Hosp, Epilepsy Res Program, Adelaide, SA 5006, Australia

Obermeier, Tanja
论文数: 0 引用数: 0
h-index: 0
机构:
Univ Med Ctr Schleswig Holstein, Inst Clin Mol Biol, Dept Neuropediat, D-24105 Kiel, Germany SA Pathol Womens & Childrens Hosp, Epilepsy Res Program, Adelaide, SA 5006, Australia

Wittig, Michael
论文数: 0 引用数: 0
h-index: 0
机构:
Univ Med Ctr Schleswig Holstein, Inst Clin Mol Biol, Dept Neuropediat, D-24105 Kiel, Germany SA Pathol Womens & Childrens Hosp, Epilepsy Res Program, Adelaide, SA 5006, Australia

Franke, Andre
论文数: 0 引用数: 0
h-index: 0
机构:
Univ Med Ctr Schleswig Holstein, Inst Clin Mol Biol, Dept Neuropediat, D-24105 Kiel, Germany SA Pathol Womens & Childrens Hosp, Epilepsy Res Program, Adelaide, SA 5006, Australia

Caglayan, Hande
论文数: 0 引用数: 0
h-index: 0
机构:
Bogazici Univ, Dept Mol Biol & Genet, Istanbul, Turkey SA Pathol Womens & Childrens Hosp, Epilepsy Res Program, Adelaide, SA 5006, Australia

Yapici, Zuhal
论文数: 0 引用数: 0
h-index: 0
机构:
Istanbul Univ, Istanbul Med Sch, Dept Child Neurol, Istanbul, Turkey SA Pathol Womens & Childrens Hosp, Epilepsy Res Program, Adelaide, SA 5006, Australia

Sander, Thomas
论文数: 0 引用数: 0
h-index: 0
机构:
Univ Cologne, Cologne Ctr Genom, Cologne, Germany SA Pathol Womens & Childrens Hosp, Epilepsy Res Program, Adelaide, SA 5006, Australia

Eichler, Evan E.
论文数: 0 引用数: 0
h-index: 0
机构:
Univ Washington, Dept Pediat, Seattle, WA 98195 USA
Univ Washington, Dept Genome Sci, Seattle, WA 98195 USA SA Pathol Womens & Childrens Hosp, Epilepsy Res Program, Adelaide, SA 5006, Australia

Scheffer, Ingrid E.
论文数: 0 引用数: 0
h-index: 0
机构:
Univ Melbourne, Dept Med, Epilepsy Res Ctr, Heidelberg, Vic 3081, Australia
Univ Melbourne, Royal Childrens Hosp, Dept Paediat, Melbourne, Vic, Australia SA Pathol Womens & Childrens Hosp, Epilepsy Res Program, Adelaide, SA 5006, Australia

Mulley, John C.
论文数: 0 引用数: 0
h-index: 0
机构:
SA Pathol Womens & Childrens Hosp, Epilepsy Res Program, Adelaide, SA 5006, Australia
Univ Adelaide, Sch Mol & Biomed Sci, Adelaide, SA 5005, Australia SA Pathol Womens & Childrens Hosp, Epilepsy Res Program, Adelaide, SA 5006, Australia

Berkovic, Samuel F.
论文数: 0 引用数: 0
h-index: 0
机构:
Univ Melbourne, Dept Med, Epilepsy Res Ctr, Heidelberg, Vic 3081, Australia SA Pathol Womens & Childrens Hosp, Epilepsy Res Program, Adelaide, SA 5006, Australia
[74]
3q29 Microdeletion: A mental Retardation Disorder Unassociated With a Recognizable Phenotype in Two Mother-Daughter Pairs
[J].
Digilio, Maria Cristina
;
Bernardini, Laura
;
Mingarelli, Rita
;
Capolino, Rossella
;
Capalbo, Anna
;
Giuffrida, Maria Grazia
;
Versacci, Paolo
;
Novelli, Antonio
;
Dallapiccola, Bruno
.
AMERICAN JOURNAL OF MEDICAL GENETICS PART A,
2009, 149A (08)
:1777-1781

Digilio, Maria Cristina
论文数: 0 引用数: 0
h-index: 0
机构:
Bambino Gesu Pediat Hosp, IRCCS, Dept Med Genet, I-00165 Rome, Italy Bambino Gesu Pediat Hosp, IRCCS, Dept Med Genet, I-00165 Rome, Italy

Bernardini, Laura
论文数: 0 引用数: 0
h-index: 0
机构:
San Giovanni Rotondo & CSS Mendel Inst, Casa Sollievo Sofferenza IRCCS, Rome, Italy Bambino Gesu Pediat Hosp, IRCCS, Dept Med Genet, I-00165 Rome, Italy

Mingarelli, Rita
论文数: 0 引用数: 0
h-index: 0
机构:
San Giovanni Rotondo & CSS Mendel Inst, Casa Sollievo Sofferenza IRCCS, Rome, Italy Bambino Gesu Pediat Hosp, IRCCS, Dept Med Genet, I-00165 Rome, Italy

Capolino, Rossella
论文数: 0 引用数: 0
h-index: 0
机构:
Bambino Gesu Pediat Hosp, IRCCS, Dept Med Genet, I-00165 Rome, Italy Bambino Gesu Pediat Hosp, IRCCS, Dept Med Genet, I-00165 Rome, Italy

Capalbo, Anna
论文数: 0 引用数: 0
h-index: 0
机构:
San Giovanni Rotondo & CSS Mendel Inst, Casa Sollievo Sofferenza IRCCS, Rome, Italy Bambino Gesu Pediat Hosp, IRCCS, Dept Med Genet, I-00165 Rome, Italy

Giuffrida, Maria Grazia
论文数: 0 引用数: 0
h-index: 0
机构:
San Giovanni Rotondo & CSS Mendel Inst, Casa Sollievo Sofferenza IRCCS, Rome, Italy Bambino Gesu Pediat Hosp, IRCCS, Dept Med Genet, I-00165 Rome, Italy

Versacci, Paolo
论文数: 0 引用数: 0
h-index: 0
机构:
Univ Roma La Sapienza, Dept Pediat, Rome, Italy Bambino Gesu Pediat Hosp, IRCCS, Dept Med Genet, I-00165 Rome, Italy

Novelli, Antonio
论文数: 0 引用数: 0
h-index: 0
机构:
San Giovanni Rotondo & CSS Mendel Inst, Casa Sollievo Sofferenza IRCCS, Rome, Italy Bambino Gesu Pediat Hosp, IRCCS, Dept Med Genet, I-00165 Rome, Italy

Dallapiccola, Bruno
论文数: 0 引用数: 0
h-index: 0
机构:
San Giovanni Rotondo & CSS Mendel Inst, Casa Sollievo Sofferenza IRCCS, Rome, Italy Bambino Gesu Pediat Hosp, IRCCS, Dept Med Genet, I-00165 Rome, Italy
[75]
Spectrum of clinical variability in familial deletion 22q11.2: from full manifestation to extremely mild clinical anomalies
[J].
Digilio, MC
;
Angioni, A
;
De Santis, M
;
Lombardo, A
;
Giannotti, A
;
Dallapiccola, B
;
Marino, B
.
CLINICAL GENETICS,
2003, 63 (04)
:308-313

Digilio, MC
论文数: 0 引用数: 0
h-index: 0
机构: Bambino Gesu Pediat Hosp, Dept Med Genet, I-00165 Rome, Italy

Angioni, A
论文数: 0 引用数: 0
h-index: 0
机构: Bambino Gesu Pediat Hosp, Dept Med Genet, I-00165 Rome, Italy

De Santis, M
论文数: 0 引用数: 0
h-index: 0
机构: Bambino Gesu Pediat Hosp, Dept Med Genet, I-00165 Rome, Italy

Lombardo, A
论文数: 0 引用数: 0
h-index: 0
机构: Bambino Gesu Pediat Hosp, Dept Med Genet, I-00165 Rome, Italy

Giannotti, A
论文数: 0 引用数: 0
h-index: 0
机构: Bambino Gesu Pediat Hosp, Dept Med Genet, I-00165 Rome, Italy

Dallapiccola, B
论文数: 0 引用数: 0
h-index: 0
机构: Bambino Gesu Pediat Hosp, Dept Med Genet, I-00165 Rome, Italy

Marino, B
论文数: 0 引用数: 0
h-index: 0
机构: Bambino Gesu Pediat Hosp, Dept Med Genet, I-00165 Rome, Italy
[76]
Web-Based Genome-Wide Association Study Identifies Two Novel Loci and a Substantial Genetic Component for Parkinson's Disease
[J].
Do, Chuong B.
;
Tung, Joyce Y.
;
Dorfman, Elizabeth
;
Kiefer, Amy K.
;
Drabant, Emily M.
;
Francke, Uta
;
Mountain, Joanna L.
;
Goldman, Samuel M.
;
Tanner, Caroline M.
;
Langston, J. William
;
Wojcicki, Anne
;
Eriksson, Nicholas
.
PLOS GENETICS,
2011, 7 (06)

Do, Chuong B.
论文数: 0 引用数: 0
h-index: 0
机构:
23andMe, Mountain View, CA USA 23andMe, Mountain View, CA USA

Tung, Joyce Y.
论文数: 0 引用数: 0
h-index: 0
机构:
23andMe, Mountain View, CA USA 23andMe, Mountain View, CA USA

Dorfman, Elizabeth
论文数: 0 引用数: 0
h-index: 0
机构:
23andMe, Mountain View, CA USA 23andMe, Mountain View, CA USA

Kiefer, Amy K.
论文数: 0 引用数: 0
h-index: 0
机构:
23andMe, Mountain View, CA USA 23andMe, Mountain View, CA USA

Drabant, Emily M.
论文数: 0 引用数: 0
h-index: 0
机构:
23andMe, Mountain View, CA USA 23andMe, Mountain View, CA USA

Francke, Uta
论文数: 0 引用数: 0
h-index: 0
机构:
23andMe, Mountain View, CA USA 23andMe, Mountain View, CA USA

Mountain, Joanna L.
论文数: 0 引用数: 0
h-index: 0
机构:
23andMe, Mountain View, CA USA 23andMe, Mountain View, CA USA

Goldman, Samuel M.
论文数: 0 引用数: 0
h-index: 0
机构:
Parkinsons Inst, Sunnyvale, CA USA 23andMe, Mountain View, CA USA

Tanner, Caroline M.
论文数: 0 引用数: 0
h-index: 0
机构:
Parkinsons Inst, Sunnyvale, CA USA 23andMe, Mountain View, CA USA

Langston, J. William
论文数: 0 引用数: 0
h-index: 0
机构:
Parkinsons Inst, Sunnyvale, CA USA 23andMe, Mountain View, CA USA

Wojcicki, Anne
论文数: 0 引用数: 0
h-index: 0
机构:
23andMe, Mountain View, CA USA 23andMe, Mountain View, CA USA

Eriksson, Nicholas
论文数: 0 引用数: 0
h-index: 0
机构:
23andMe, Mountain View, CA USA 23andMe, Mountain View, CA USA
[77]
Nine patients with a microdeletion 15q11.2 between breakpoints 1 and 2 of the Prader-Willi critical region, possibly associated with behavioural disturbances
[J].
Doornbos, Marianne
;
Sikkema-Raddatz, Birgit
;
Ruijvenkamp, Claudia A. L.
;
Dijkhuizen, Trijnie
;
Bijlsma, Emilia K.
;
Gijsbers, Antoinet C. J.
;
Hilhorst-Hofstee, Yvonne
;
Hordijk, Roel
;
Verbruggen, Krijn T.
;
Kerstjens-Frederikse, W. S.
;
van Essen, Ton
;
Kok, Klaas
;
van Silfhout, Anneke T.
;
Breuning, Martijn
;
van Ravenswaaij-Arts, Conny M. A.
.
EUROPEAN JOURNAL OF MEDICAL GENETICS,
2009, 52 (2-3)
:108-115

Doornbos, Marianne
论文数: 0 引用数: 0
h-index: 0
机构:
Univ Groningen, Univ Med Ctr Groningen, Beatrix Childrens Hosp, NL-9700 RB Groningen, Netherlands
Albert Schweitzer Hosp, Dept Paediat, Dordrecht, Netherlands Univ Groningen, Univ Med Ctr Groningen, Dept Genet, NL-9700 RB Groningen, Netherlands

Sikkema-Raddatz, Birgit
论文数: 0 引用数: 0
h-index: 0
机构:
Univ Groningen, Univ Med Ctr Groningen, Dept Genet, NL-9700 RB Groningen, Netherlands Univ Groningen, Univ Med Ctr Groningen, Dept Genet, NL-9700 RB Groningen, Netherlands

Ruijvenkamp, Claudia A. L.
论文数: 0 引用数: 0
h-index: 0
机构:
Leiden Univ, Med Ctr, Dept Clin Genet, NL-2300 RA Leiden, Netherlands Univ Groningen, Univ Med Ctr Groningen, Dept Genet, NL-9700 RB Groningen, Netherlands

Dijkhuizen, Trijnie
论文数: 0 引用数: 0
h-index: 0
机构:
Univ Groningen, Univ Med Ctr Groningen, Dept Genet, NL-9700 RB Groningen, Netherlands Univ Groningen, Univ Med Ctr Groningen, Dept Genet, NL-9700 RB Groningen, Netherlands

Bijlsma, Emilia K.
论文数: 0 引用数: 0
h-index: 0
机构:
Leiden Univ, Med Ctr, Dept Clin Genet, NL-2300 RA Leiden, Netherlands Univ Groningen, Univ Med Ctr Groningen, Dept Genet, NL-9700 RB Groningen, Netherlands

Gijsbers, Antoinet C. J.
论文数: 0 引用数: 0
h-index: 0
机构:
Leiden Univ, Med Ctr, Dept Clin Genet, NL-2300 RA Leiden, Netherlands Univ Groningen, Univ Med Ctr Groningen, Dept Genet, NL-9700 RB Groningen, Netherlands

Hilhorst-Hofstee, Yvonne
论文数: 0 引用数: 0
h-index: 0
机构:
Leiden Univ, Med Ctr, Dept Clin Genet, NL-2300 RA Leiden, Netherlands Univ Groningen, Univ Med Ctr Groningen, Dept Genet, NL-9700 RB Groningen, Netherlands

Hordijk, Roel
论文数: 0 引用数: 0
h-index: 0
机构:
Univ Groningen, Univ Med Ctr Groningen, Dept Genet, NL-9700 RB Groningen, Netherlands Univ Groningen, Univ Med Ctr Groningen, Dept Genet, NL-9700 RB Groningen, Netherlands

Verbruggen, Krijn T.
论文数: 0 引用数: 0
h-index: 0
机构:
Univ Groningen, Univ Med Ctr Groningen, Beatrix Childrens Hosp, NL-9700 RB Groningen, Netherlands Univ Groningen, Univ Med Ctr Groningen, Dept Genet, NL-9700 RB Groningen, Netherlands

Kerstjens-Frederikse, W. S.
论文数: 0 引用数: 0
h-index: 0
机构:
Univ Groningen, Univ Med Ctr Groningen, Dept Genet, NL-9700 RB Groningen, Netherlands Univ Groningen, Univ Med Ctr Groningen, Dept Genet, NL-9700 RB Groningen, Netherlands

van Essen, Ton
论文数: 0 引用数: 0
h-index: 0
机构:
Univ Groningen, Univ Med Ctr Groningen, Dept Genet, NL-9700 RB Groningen, Netherlands Univ Groningen, Univ Med Ctr Groningen, Dept Genet, NL-9700 RB Groningen, Netherlands

论文数: 引用数:
h-index:
机构:

van Silfhout, Anneke T.
论文数: 0 引用数: 0
h-index: 0
机构:
Univ Groningen, Univ Med Ctr Groningen, Dept Genet, NL-9700 RB Groningen, Netherlands Univ Groningen, Univ Med Ctr Groningen, Dept Genet, NL-9700 RB Groningen, Netherlands

Breuning, Martijn
论文数: 0 引用数: 0
h-index: 0
机构:
Leiden Univ, Med Ctr, Dept Clin Genet, NL-2300 RA Leiden, Netherlands Univ Groningen, Univ Med Ctr Groningen, Dept Genet, NL-9700 RB Groningen, Netherlands

van Ravenswaaij-Arts, Conny M. A.
论文数: 0 引用数: 0
h-index: 0
机构:
Univ Groningen, Univ Med Ctr Groningen, Dept Genet, NL-9700 RB Groningen, Netherlands Univ Groningen, Univ Med Ctr Groningen, Dept Genet, NL-9700 RB Groningen, Netherlands
[78]
The advent of personal genome sequencing
[J].
Drmanac, Radoje
.
GENETICS IN MEDICINE,
2011, 13 (03)
:188-190

Drmanac, Radoje
论文数: 0 引用数: 0
h-index: 0
机构:
Complete Genom Inc, Mountain View, CA 94043 USA Complete Genom Inc, Mountain View, CA 94043 USA
[79]
EBERHARD G, 1975, Neuropsychobiology, V1, P211, DOI 10.1159/000117496
[80]
Low-copy repeats mediate the common 3-Mb deletion in patients with velo-cardio-facial syndrome
[J].
Edelmann, L
;
Pandita, RK
;
Morrow, BE
.
AMERICAN JOURNAL OF HUMAN GENETICS,
1999, 64 (04)
:1076-1086

Edelmann, L
论文数: 0 引用数: 0
h-index: 0
机构:
Yeshiva Univ Albert Einstein Coll Med, Dept Mol Genet, Bronx, NY 10461 USA Yeshiva Univ Albert Einstein Coll Med, Dept Mol Genet, Bronx, NY 10461 USA

Pandita, RK
论文数: 0 引用数: 0
h-index: 0
机构:
Yeshiva Univ Albert Einstein Coll Med, Dept Mol Genet, Bronx, NY 10461 USA Yeshiva Univ Albert Einstein Coll Med, Dept Mol Genet, Bronx, NY 10461 USA

Morrow, BE
论文数: 0 引用数: 0
h-index: 0
机构:
Yeshiva Univ Albert Einstein Coll Med, Dept Mol Genet, Bronx, NY 10461 USA Yeshiva Univ Albert Einstein Coll Med, Dept Mol Genet, Bronx, NY 10461 USA