共 38 条
[1]
Legislation on direct-to-consumer genetic testing in seven European countries
[J].
Borry, Pascal
;
van Hellemondt, Rachel E.
;
Sprumont, Dominique
;
Duarte Jales, Camilla Fittipaldi
;
Rial-Sebbag, Emmanuelle
;
Spranger, Tade Matthias
;
Curren, Liam
;
Kaye, Jane
;
Nys, Herman
;
Howard, Heidi
.
EUROPEAN JOURNAL OF HUMAN GENETICS,
2012, 20 (07)
:715-721

论文数: 引用数:
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van Hellemondt, Rachel E.
论文数: 0 引用数: 0
h-index: 0
机构:
Leiden Univ Med Ctr, Leiden, Netherlands Katholieke Univ Leuven, Ctr Biomed Eth & Law, B-3000 Louvain, Belgium

Sprumont, Dominique
论文数: 0 引用数: 0
h-index: 0
机构:
Univ Neuchatel, Inst Hlth Law, CH-2000 Neuchatel, Switzerland Katholieke Univ Leuven, Ctr Biomed Eth & Law, B-3000 Louvain, Belgium

Duarte Jales, Camilla Fittipaldi
论文数: 0 引用数: 0
h-index: 0
机构:
Portuguese Catholic Univ, Inst Bioeth, Porto, Portugal Katholieke Univ Leuven, Ctr Biomed Eth & Law, B-3000 Louvain, Belgium

Rial-Sebbag, Emmanuelle
论文数: 0 引用数: 0
h-index: 0
机构:
Univ Toulouse 3, Dept Epidemiol & Sante publ, INSERM, Univ Toulouse,UMR U 1027, F-31062 Toulouse, France Katholieke Univ Leuven, Ctr Biomed Eth & Law, B-3000 Louvain, Belgium

Spranger, Tade Matthias
论文数: 0 引用数: 0
h-index: 0
机构:
Univ Bonn, Inst Publ Law, Bonn, Germany Katholieke Univ Leuven, Ctr Biomed Eth & Law, B-3000 Louvain, Belgium

Curren, Liam
论文数: 0 引用数: 0
h-index: 0
机构:
Univ Oxford, HeLEX Ctr Hlth Law & Emerging Technol, Oxford, England Katholieke Univ Leuven, Ctr Biomed Eth & Law, B-3000 Louvain, Belgium

Kaye, Jane
论文数: 0 引用数: 0
h-index: 0
机构:
Univ Oxford, HeLEX Ctr Hlth Law & Emerging Technol, Oxford, England Katholieke Univ Leuven, Ctr Biomed Eth & Law, B-3000 Louvain, Belgium

Nys, Herman
论文数: 0 引用数: 0
h-index: 0
机构:
Katholieke Univ Leuven, Ctr Biomed Eth & Law, B-3000 Louvain, Belgium Katholieke Univ Leuven, Ctr Biomed Eth & Law, B-3000 Louvain, Belgium

Howard, Heidi
论文数: 0 引用数: 0
h-index: 0
机构:
Univ Basel, Inst BioMed Eth, Basel, Switzerland Katholieke Univ Leuven, Ctr Biomed Eth & Law, B-3000 Louvain, Belgium
[2]
What Happens to Children With Epilepsy When They Become Adults? Some Facts and Opinions
[J].
Camfield, Peter R.
;
Camfield, Carol S.
.
PEDIATRIC NEUROLOGY,
2014, 51 (01)
:17-23

Camfield, Peter R.
论文数: 0 引用数: 0
h-index: 0
机构:
Dalhousie Univ, Dept Pediat, Halifax, NS B3K 6R8, Canada
IWK Hlth Ctr, Halifax, NS B3K 6R8, Canada Dalhousie Univ, Dept Pediat, Halifax, NS B3K 6R8, Canada

Camfield, Carol S.
论文数: 0 引用数: 0
h-index: 0
机构: Dalhousie Univ, Dept Pediat, Halifax, NS B3K 6R8, Canada
[3]
Using next-generation sequencing as a genetic diagnostic tool in rare autosomal recessive neurologic Mendelian disorders
[J].
Chen, Zhao
;
Wang, Jun-ling
;
Tang, Bei-sha
;
Sun, Zhan-fang
;
Shi, Yu-ting
;
Shen, Lu
;
Lei, Li-fang
;
Wei, Xiao-ming
;
Xiao, Jing-jing
;
Hu, Zheng-mao
;
Pan, Qian
;
Xia, Kun
;
Zhang, Qing-yan
;
Dai, Mei-zhi
;
Liu, Yu
;
Ashizawa, Tetsuo
;
Jiang, Hong
.
NEUROBIOLOGY OF AGING,
2013, 34 (10)
:2442.e11-2442.e17

Chen, Zhao
论文数: 0 引用数: 0
h-index: 0
机构:
Cent S Univ, Xiangya Hosp, Dept Neurol, Changsha 410008, Hunan, Peoples R China Cent S Univ, Xiangya Hosp, Dept Neurol, Changsha 410008, Hunan, Peoples R China

Wang, Jun-ling
论文数: 0 引用数: 0
h-index: 0
机构:
Cent S Univ, Xiangya Hosp, Dept Neurol, Changsha 410008, Hunan, Peoples R China Cent S Univ, Xiangya Hosp, Dept Neurol, Changsha 410008, Hunan, Peoples R China

Tang, Bei-sha
论文数: 0 引用数: 0
h-index: 0
机构:
Cent S Univ, Xiangya Hosp, Dept Neurol, Changsha 410008, Hunan, Peoples R China
Cent S Univ, Neurodegenerat Disorders Res Ctr, Changsha 410008, Hunan, Peoples R China
Cent S Univ, State Key Lab Med Genet, Changsha 410008, Hunan, Peoples R China Cent S Univ, Xiangya Hosp, Dept Neurol, Changsha 410008, Hunan, Peoples R China

Sun, Zhan-fang
论文数: 0 引用数: 0
h-index: 0
机构:
Cent S Univ, Xiangya Hosp, Dept Neurol, Changsha 410008, Hunan, Peoples R China Cent S Univ, Xiangya Hosp, Dept Neurol, Changsha 410008, Hunan, Peoples R China

Shi, Yu-ting
论文数: 0 引用数: 0
h-index: 0
机构:
Cent S Univ, Xiangya Hosp, Dept Neurol, Changsha 410008, Hunan, Peoples R China Cent S Univ, Xiangya Hosp, Dept Neurol, Changsha 410008, Hunan, Peoples R China

Shen, Lu
论文数: 0 引用数: 0
h-index: 0
机构:
Cent S Univ, Xiangya Hosp, Dept Neurol, Changsha 410008, Hunan, Peoples R China Cent S Univ, Xiangya Hosp, Dept Neurol, Changsha 410008, Hunan, Peoples R China

Lei, Li-fang
论文数: 0 引用数: 0
h-index: 0
机构:
Cent S Univ, Xiangya Hosp 3, Dept Neurol, Changsha 410008, Hunan, Peoples R China Cent S Univ, Xiangya Hosp, Dept Neurol, Changsha 410008, Hunan, Peoples R China

Wei, Xiao-ming
论文数: 0 引用数: 0
h-index: 0
机构:
BGI Shenzhen, Shenzhen, Guangdong, Peoples R China Cent S Univ, Xiangya Hosp, Dept Neurol, Changsha 410008, Hunan, Peoples R China

Xiao, Jing-jing
论文数: 0 引用数: 0
h-index: 0
机构:
BGI Shenzhen, Shenzhen, Guangdong, Peoples R China Cent S Univ, Xiangya Hosp, Dept Neurol, Changsha 410008, Hunan, Peoples R China

Hu, Zheng-mao
论文数: 0 引用数: 0
h-index: 0
机构:
Cent S Univ, State Key Lab Med Genet, Changsha 410008, Hunan, Peoples R China Cent S Univ, Xiangya Hosp, Dept Neurol, Changsha 410008, Hunan, Peoples R China

Pan, Qian
论文数: 0 引用数: 0
h-index: 0
机构:
Cent S Univ, State Key Lab Med Genet, Changsha 410008, Hunan, Peoples R China Cent S Univ, Xiangya Hosp, Dept Neurol, Changsha 410008, Hunan, Peoples R China

Xia, Kun
论文数: 0 引用数: 0
h-index: 0
机构:
Cent S Univ, State Key Lab Med Genet, Changsha 410008, Hunan, Peoples R China Cent S Univ, Xiangya Hosp, Dept Neurol, Changsha 410008, Hunan, Peoples R China

Zhang, Qing-yan
论文数: 0 引用数: 0
h-index: 0
机构:
BGI Shenzhen, Shenzhen, Guangdong, Peoples R China Cent S Univ, Xiangya Hosp, Dept Neurol, Changsha 410008, Hunan, Peoples R China

Dai, Mei-zhi
论文数: 0 引用数: 0
h-index: 0
机构:
BGI Shenzhen, Shenzhen, Guangdong, Peoples R China Cent S Univ, Xiangya Hosp, Dept Neurol, Changsha 410008, Hunan, Peoples R China

Liu, Yu
论文数: 0 引用数: 0
h-index: 0
机构:
Cent S Univ, Xiangya Hosp, Dept Neurol, Changsha 410008, Hunan, Peoples R China Cent S Univ, Xiangya Hosp, Dept Neurol, Changsha 410008, Hunan, Peoples R China

Ashizawa, Tetsuo
论文数: 0 引用数: 0
h-index: 0
机构:
Univ Florida, Dept Neurol, Gainesville, FL USA Cent S Univ, Xiangya Hosp, Dept Neurol, Changsha 410008, Hunan, Peoples R China

Jiang, Hong
论文数: 0 引用数: 0
h-index: 0
机构:
Cent S Univ, Xiangya Hosp, Dept Neurol, Changsha 410008, Hunan, Peoples R China
Cent S Univ, Neurodegenerat Disorders Res Ctr, Changsha 410008, Hunan, Peoples R China Cent S Univ, Xiangya Hosp, Dept Neurol, Changsha 410008, Hunan, Peoples R China
[4]
Managing Incidental Genomic Findings in Clinical Trials: Fulfillment of the Principle of Justice
[J].
Dal-Re, Rafael
;
Katsanis, Nicholas
;
Katsanis, Sara
;
Parker, Lisa S.
;
Ayuso, Carmen
.
PLOS MEDICINE,
2014, 11 (01)

Dal-Re, Rafael
论文数: 0 引用数: 0
h-index: 0
机构:
Pasqual Maragall Fdn, Clin Res Program, Barcelona, Spain Pasqual Maragall Fdn, Clin Res Program, Barcelona, Spain

论文数: 引用数:
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Katsanis, Sara
论文数: 0 引用数: 0
h-index: 0
机构:
Duke Univ, Duke Inst Genome Sci & Policy, Durham, NC USA Pasqual Maragall Fdn, Clin Res Program, Barcelona, Spain

Parker, Lisa S.
论文数: 0 引用数: 0
h-index: 0
机构:
Univ Pittsburgh, Ctr Bioeth & Hlth Law, Pittsburgh, PA USA Pasqual Maragall Fdn, Clin Res Program, Barcelona, Spain

Ayuso, Carmen
论文数: 0 引用数: 0
h-index: 0
机构:
Jimenez Diaz Fdn Univ Hosp IIS FJD, Dept Genet, Hlth Res Inst, Madrid, Spain
Inst Salud Carlos III, CIBERER Ctr Invest Biomedica Red Enfermedades Rar, Madrid, Spain Pasqual Maragall Fdn, Clin Res Program, Barcelona, Spain
[5]
Genetic advances spark a revolution in dystonia phenotyping
[J].
de Koning, Tom J.
;
Tijssen, Marina A. J.
.
NATURE REVIEWS NEUROLOGY,
2015, 11 (02)
:78-79

de Koning, Tom J.
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 Neurol, NL-9700 RB Groningen, Netherlands Univ Groningen, Univ Med Ctr Groningen, Dept Genet, NL-9700 RB Groningen, Netherlands

Tijssen, Marina A. J.
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 Neurol, NL-9700 RB Groningen, Netherlands Univ Groningen, Univ Med Ctr Groningen, Dept Genet, NL-9700 RB Groningen, Netherlands
[6]
Genetic testing among Spanish pediatric neurologists: Knowledge, attitudes and practices
[J].
Dominguez-Carral, J.
;
Lopez-Pison, J.
;
Macaya, A.
;
Bueno Campana, M.
;
Garcia-Perez, M. A.
;
Natera-de Benito, D.
.
EUROPEAN JOURNAL OF MEDICAL GENETICS,
2017, 60 (02)
:124-129

Dominguez-Carral, J.
论文数: 0 引用数: 0
h-index: 0
机构:
Hosp Univ Torrejon, Dept Pediat, Madrid, Spain Hosp Univ Torrejon, Dept Pediat, Madrid, Spain

Lopez-Pison, J.
论文数: 0 引用数: 0
h-index: 0
机构:
Hosp Univ Miguel Servet, Dept Pediat Neurol, Zaragoza, Spain Hosp Univ Torrejon, Dept Pediat, Madrid, Spain

Macaya, A.
论文数: 0 引用数: 0
h-index: 0
机构:
Hosp Univ Vall dHebron, Dept Pediat Neurol, Barcelona, Spain Hosp Univ Torrejon, Dept Pediat, Madrid, Spain

Bueno Campana, M.
论文数: 0 引用数: 0
h-index: 0
机构:
Hosp Univ Fdn Alcorcon, Dept Pediat, Madrid, Spain Hosp Univ Torrejon, Dept Pediat, Madrid, Spain

Garcia-Perez, M. A.
论文数: 0 引用数: 0
h-index: 0
机构:
Hosp Univ Fdn Alcorcon, Dept Pediat, Madrid, Spain Hosp Univ Torrejon, Dept Pediat, Madrid, Spain

Natera-de Benito, D.
论文数: 0 引用数: 0
h-index: 0
机构:
Hosp Univ Fuenlabrada, Dept Pediat, Madrid, Spain Hosp Univ Torrejon, Dept Pediat, Madrid, Spain
[7]
Use of Whole Genome Sequencing for Diagnosis and Discovery in the Cancer Genetics Clinic
[J].
Foley, Samantha B.
;
Rios, Jonathan J.
;
Mgbemena, Victoria E.
;
Robinson, Linda S.
;
Hampel, Heather L.
;
Toland, Amanda E.
;
Durham, Leslie
;
Ross, Theodora S.
.
EBIOMEDICINE,
2015, 2 (01)
:74-81

Foley, Samantha B.
论文数: 0 引用数: 0
h-index: 0
机构:
Univ Texas SW Med Ctr Dallas, Dept Internal Med, Dallas, TX 75390 USA Univ Texas SW Med Ctr Dallas, Dept Internal Med, Dallas, TX 75390 USA

Rios, Jonathan J.
论文数: 0 引用数: 0
h-index: 0
机构:
Texas Scottish Rite Hosp Children, Sarah M & Charles E Seay Ctr Musculoskeletal Res, Dallas, TX 75219 USA
Univ Texas SW Med Ctr Dallas, Dept Pediat, McDermott Ctr Human Growth & Dev, Dallas, TX 75390 USA
Univ Texas SW Med Ctr Dallas, Dept Orthopaed Surg, Dallas, TX 75390 USA Univ Texas SW Med Ctr Dallas, Dept Internal Med, Dallas, TX 75390 USA

Mgbemena, Victoria E.
论文数: 0 引用数: 0
h-index: 0
机构:
Univ Texas SW Med Ctr Dallas, Dept Internal Med, Dallas, TX 75390 USA Univ Texas SW Med Ctr Dallas, Dept Internal Med, Dallas, TX 75390 USA

Robinson, Linda S.
论文数: 0 引用数: 0
h-index: 0
机构:
Univ Texas SW Med Ctr Dallas, Dept Canc Genet, Dallas, TX 75390 USA Univ Texas SW Med Ctr Dallas, Dept Internal Med, Dallas, TX 75390 USA

Hampel, Heather L.
论文数: 0 引用数: 0
h-index: 0
机构:
Ohio State Univ, Dept Human Genet, Columbus, OH 43210 USA Univ Texas SW Med Ctr Dallas, Dept Internal Med, Dallas, TX 75390 USA

Toland, Amanda E.
论文数: 0 引用数: 0
h-index: 0
机构:
Ohio State Univ, Dept Human Genet, Columbus, OH 43210 USA Univ Texas SW Med Ctr Dallas, Dept Internal Med, Dallas, TX 75390 USA

Durham, Leslie
论文数: 0 引用数: 0
h-index: 0
机构:
Univ Texas SW Med Ctr Dallas, Dept Internal Med, Dallas, TX 75390 USA
Texas Scottish Rite Hosp Children, Sarah M & Charles E Seay Ctr Musculoskeletal Res, Dallas, TX 75219 USA Univ Texas SW Med Ctr Dallas, Dept Internal Med, Dallas, TX 75390 USA

Ross, Theodora S.
论文数: 0 引用数: 0
h-index: 0
机构:
Univ Texas SW Med Ctr Dallas, Dept Internal Med, Dallas, TX 75390 USA
Univ Texas SW Med Ctr Dallas, Dept Canc Genet, Dallas, TX 75390 USA Univ Texas SW Med Ctr Dallas, Dept Internal Med, Dallas, TX 75390 USA
[8]
Next-generation sequencing diagnostics for neurological diseases/disorders: from a clinical perspective
[J].
Foo, Jia Nee
;
Liu, Jianjun
;
Tan, Eng-King
.
HUMAN GENETICS,
2013, 132 (07)
:721-734

Foo, Jia Nee
论文数: 0 引用数: 0
h-index: 0
机构:
ASTAR, Human Genet, Genome Inst Singapore, Singapore 138672, Singapore ASTAR, Human Genet, Genome Inst Singapore, Singapore 138672, Singapore

Liu, Jianjun
论文数: 0 引用数: 0
h-index: 0
机构:
ASTAR, Human Genet, Genome Inst Singapore, Singapore 138672, Singapore ASTAR, Human Genet, Genome Inst Singapore, Singapore 138672, Singapore

Tan, Eng-King
论文数: 0 引用数: 0
h-index: 0
机构:
Singapore Gen Hosp, Dept Neurol, Natl Neurosci Inst, Duke Natl Univ Singapore Grad Med Sch, Block 1 Level 3,Outram Rd, Singapore 169108, Singapore ASTAR, Human Genet, Genome Inst Singapore, Singapore 138672, Singapore
[9]
Whole-genome and whole-exome sequencing in neurological diseases
[J].
Foo, Jia-Nee
;
Liu, Jian-Jun
;
Tan, Eng-King
.
NATURE REVIEWS NEUROLOGY,
2012, 8 (09)
:508-517

Foo, Jia-Nee
论文数: 0 引用数: 0
h-index: 0
机构:
ASTAR, Genome Inst Singapore, Singapore 138672, Singapore Duke Natl Univ Singapore, Grad Sch Med, Singapore Gen Hosp, Dept Neurol,Natl Neurosci Inst, Block 1,Level 3,Outram Rd, Singapore 169108, Singapore

Liu, Jian-Jun
论文数: 0 引用数: 0
h-index: 0
机构:
ASTAR, Genome Inst Singapore, Singapore 138672, Singapore Duke Natl Univ Singapore, Grad Sch Med, Singapore Gen Hosp, Dept Neurol,Natl Neurosci Inst, Block 1,Level 3,Outram Rd, Singapore 169108, Singapore

Tan, Eng-King
论文数: 0 引用数: 0
h-index: 0
机构:
Duke Natl Univ Singapore, Grad Sch Med, Singapore Gen Hosp, Dept Neurol,Natl Neurosci Inst, Block 1,Level 3,Outram Rd, Singapore 169108, Singapore Duke Natl Univ Singapore, Grad Sch Med, Singapore Gen Hosp, Dept Neurol,Natl Neurosci Inst, Block 1,Level 3,Outram Rd, Singapore 169108, Singapore
[10]
The National Institutes of Health Undiagnosed Diseases Program: insights into rare diseases
[J].
Gahl, William A.
;
Markello, Thomas C.
;
Toro, Camilo
;
Fajardo, Karin Fuentes
;
Sincan, Murat
;
Gill, Fred
;
Carlson-Donohoe, Hannah
;
Gropman, Andrea
;
Pierson, Tyler Mark
;
Golas, Gretchen
;
Wolfe, Lynne
;
Groden, Catherine
;
Godfrey, Rena
;
Nehrebecky, Michele
;
Wahl, Colleen
;
Landis, Dennis M. D.
;
Yang, Sandra
;
Madeo, Anne
;
Mullikin, James C.
;
Boerkoel, Cornelius F.
;
Tifft, Cynthia J.
;
Adams, David
.
GENETICS IN MEDICINE,
2012, 14 (01)
:51-59

Gahl, William A.
论文数: 0 引用数: 0
h-index: 0
机构:
NIH, Undiagnosed Dis Program, Bethesda, MD 20892 USA
NHGRI, Off Clin Director, NIH, Bethesda, MD 20892 USA
NHGRI, Med Genet Branch, NIH, Bethesda, MD 20892 USA NIH, Undiagnosed Dis Program, Bethesda, MD 20892 USA

Markello, Thomas C.
论文数: 0 引用数: 0
h-index: 0
机构:
NHGRI, Off Clin Director, NIH, Bethesda, MD 20892 USA NIH, Undiagnosed Dis Program, Bethesda, MD 20892 USA

Toro, Camilo
论文数: 0 引用数: 0
h-index: 0
机构:
NIH, Undiagnosed Dis Program, Bethesda, MD 20892 USA NIH, Undiagnosed Dis Program, Bethesda, MD 20892 USA

Fajardo, Karin Fuentes
论文数: 0 引用数: 0
h-index: 0
机构:
NIH, Undiagnosed Dis Program, Bethesda, MD 20892 USA NIH, Undiagnosed Dis Program, Bethesda, MD 20892 USA

Sincan, Murat
论文数: 0 引用数: 0
h-index: 0
机构:
NHGRI, Med Genet Branch, NIH, Bethesda, MD 20892 USA NIH, Undiagnosed Dis Program, Bethesda, MD 20892 USA

Gill, Fred
论文数: 0 引用数: 0
h-index: 0
机构:
NIH, Ctr Clin, Bethesda, MD 20892 USA NIH, Undiagnosed Dis Program, Bethesda, MD 20892 USA

Carlson-Donohoe, Hannah
论文数: 0 引用数: 0
h-index: 0
机构:
NHGRI, Med Genet Branch, NIH, Bethesda, MD 20892 USA NIH, Undiagnosed Dis Program, Bethesda, MD 20892 USA

Gropman, Andrea
论文数: 0 引用数: 0
h-index: 0
机构:
NHGRI, Off Clin Director, NIH, Bethesda, MD 20892 USA
Childrens Natl Med Ctr, Dept Neurol, Washington, DC 20010 USA NIH, Undiagnosed Dis Program, Bethesda, MD 20892 USA

Pierson, Tyler Mark
论文数: 0 引用数: 0
h-index: 0
机构:
NIH, Undiagnosed Dis Program, Bethesda, MD 20892 USA
Natl Inst Neurol Disorders & Stroke, Neurogenet Branch, NIH, Bethesda, MD USA NIH, Undiagnosed Dis Program, Bethesda, MD 20892 USA

Golas, Gretchen
论文数: 0 引用数: 0
h-index: 0
机构:
NHGRI, Off Clin Director, NIH, Bethesda, MD 20892 USA NIH, Undiagnosed Dis Program, Bethesda, MD 20892 USA

Wolfe, Lynne
论文数: 0 引用数: 0
h-index: 0
机构:
NIH, Undiagnosed Dis Program, Bethesda, MD 20892 USA NIH, Undiagnosed Dis Program, Bethesda, MD 20892 USA

Groden, Catherine
论文数: 0 引用数: 0
h-index: 0
机构:
NIH, Undiagnosed Dis Program, Bethesda, MD 20892 USA
NHGRI, Off Clin Director, NIH, Bethesda, MD 20892 USA NIH, Undiagnosed Dis Program, Bethesda, MD 20892 USA

Godfrey, Rena
论文数: 0 引用数: 0
h-index: 0
机构:
NIH, Undiagnosed Dis Program, Bethesda, MD 20892 USA NIH, Undiagnosed Dis Program, Bethesda, MD 20892 USA

Nehrebecky, Michele
论文数: 0 引用数: 0
h-index: 0
机构:
NIH, Undiagnosed Dis Program, Bethesda, MD 20892 USA NIH, Undiagnosed Dis Program, Bethesda, MD 20892 USA

Wahl, Colleen
论文数: 0 引用数: 0
h-index: 0
机构:
NIH, Undiagnosed Dis Program, Bethesda, MD 20892 USA NIH, Undiagnosed Dis Program, Bethesda, MD 20892 USA

Landis, Dennis M. D.
论文数: 0 引用数: 0
h-index: 0
机构:
NIH, Undiagnosed Dis Program, Bethesda, MD 20892 USA NIH, Undiagnosed Dis Program, Bethesda, MD 20892 USA

Yang, Sandra
论文数: 0 引用数: 0
h-index: 0
机构:
NIH, Undiagnosed Dis Program, Bethesda, MD 20892 USA
NHGRI, Off Clin Director, NIH, Bethesda, MD 20892 USA NIH, Undiagnosed Dis Program, Bethesda, MD 20892 USA

Madeo, Anne
论文数: 0 引用数: 0
h-index: 0
机构:
NIH, Social & Behav Res Branch, Off Rare Dis Res, Off Director, Bethesda, MD 20892 USA NIH, Undiagnosed Dis Program, Bethesda, MD 20892 USA

Mullikin, James C.
论文数: 0 引用数: 0
h-index: 0
机构:
NHGRI, Intramural Sequencing Ctr, NIH, Bethesda, MD 20892 USA NIH, Undiagnosed Dis Program, Bethesda, MD 20892 USA

Boerkoel, Cornelius F.
论文数: 0 引用数: 0
h-index: 0
机构:
NIH, Undiagnosed Dis Program, Bethesda, MD 20892 USA NIH, Undiagnosed Dis Program, Bethesda, MD 20892 USA

Tifft, Cynthia J.
论文数: 0 引用数: 0
h-index: 0
机构:
NIH, Undiagnosed Dis Program, Bethesda, MD 20892 USA
NHGRI, Off Clin Director, NIH, Bethesda, MD 20892 USA NIH, Undiagnosed Dis Program, Bethesda, MD 20892 USA

Adams, David
论文数: 0 引用数: 0
h-index: 0
机构:
NIH, Undiagnosed Dis Program, Bethesda, MD 20892 USA
NHGRI, Med Genet Branch, NIH, Bethesda, MD 20892 USA NIH, Undiagnosed Dis Program, Bethesda, MD 20892 USA