Mutations in CDMP1 cause autosomal dominant brachydactyly type C

被引：211

作者：

Polinkovsky, A

Robin, NH

Thomas, JT

Irons, M

Lynn, A

Goodman, FR

Reardon, W

Kant, SG

Brunner, HG

vanderBurgt, I

Chitayat, D

McGaughran, J

Donnai, D

Luyten, FP

Warman, ML

机构：

[1] CASE WESTERN RESERVE UNIV,SCH MED,DEPT GENET,CLEVELAND,OH 44106

[2] CASE WESTERN RESERVE UNIV,SCH MED,DEPT PEDIAT,CLEVELAND,OH 44106

[3] UNIV HOSP CLEVELAND,CTR HUMAN GENET,CLEVELAND,OH 44106

[4] NIDR,CRANIOFACIAL & SKELETAL DIS BRANCH,NIH,BETHESDA,MD 20892

[5] FLOATING HOSP CHILDREN,NEW ENGLAND MED CTR,DIV GENET,BOSTON,MA

[6] INST CHILD HLTH,MOL MED UNIT,LONDON,ENGLAND

[7] INST CHILD HLTH,MOTHERCARE UNIT,CLIN GENET & FETAL MED,LONDON,ENGLAND

[8] UNIV LEIDEN HOSP,DEPT CLIN GENET,NL-2300 RC LEIDEN,NETHERLANDS

[9] UNIV NIJMEGEN HOSP,DEPT CLIN GENET,NL-6500 HB NIJMEGEN,NETHERLANDS

[10] UNIV TORONTO,HOSP SICK CHILDREN,DIV CLIN GENET,TORONTO,ON M5G 1X8,CANADA

[11] ST MARYS HOSP,DEPT CLIN GENET,MANCHESTER M13 0JH,LANCS,ENGLAND

来源：

关键词：

D O I：

10.1038/ng0997-18

中图分类号：

Q3 [遗传学];

学科分类号：

071007 ; 090102 ;

摘要：

引用

页码：18 / 19

页数：2

共 16 条

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