The mutation spectrum in Holt-Oram syndrome

被引：53

作者：

Cross, SJ

Ching, YH

Li, QY

Armstrong-Buisseret, L

Spranger, S

Lyonnet, S

Bonnet, D

Penttinen, M

Jonveaux, P

Leheup, B

Mortier, G

Van Ravenswaaij, C

Gardiner, CA

Brook, JD ^{[1
]}

Newbury-Ecob, R

机构：

[1] Univ Nottingham, Queens Med Ctr, Genet Inst, Nottingham NG7 2UH, England

[2] Univ Bremen, Ctr Human Genet & Genet Counseling, D-28359 Bremen, Germany

[3] Grp Hosp Necker Enfants Malad, Unite Rech Handicaps Genet Enfant, F-75743 Paris, France

[4] Grp Hosp Necker Enfants Malad, Serv Cardiol Pediat, F-75743 Paris 15, France

[5] Turku Univ, Cent Hosp, Clin Genet Unit, Turku 20521, Finland

[6] CHU Nancy, Serv Genet, F-54511 Vandoeuvre Nancy, France

[7] State Univ Ghent Hosp, Dept Med Genet, B-9000 Ghent, Belgium

[8] Univ Nijmegen Hosp, Dept Human Genet, NL-6500 HB Nijmegen, Netherlands

[9] St James Univ Hosp, Dept Clin Genet, Yorkshire Reg Genet Serv, Leeds LS9 7TF, W Yorkshire, England

[10] Royal Hosp Sick Children, Inst Child Hlth, Clin Genet Serv, Bristol BS2 8BJ, Avon, England

来源：

JOURNAL OF MEDICAL GENETICS | 2000年 / 37卷 / 10期

关键词：

D O I：

10.1136/jmg.37.10.785

中图分类号：

Q3 [遗传学];

学科分类号：

071007 ; 090102 ;

摘要：

引用

页码：785 / 787

页数：3

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