Partial deletion of the critical 1.5 Mb interval in Williams-Beuren syndrome -: art. no. e99

被引：43

作者：

Heller, R

Rauch, A

Lüttgen, S

Schröder, B

Winterpacht, A

机构：

[1] Oxford Radcliffe Hosp NHS Trust, Dept Clin Genet, Oxford OX3 7LJ, England

[2] Univ Hamburg, Inst Human Genet, D-22529 Hamburg, Germany

[3] Univ Erlangen Nurnberg, Inst Human Genet, D-91054 Erlangen, Germany

来源：

JOURNAL OF MEDICAL GENETICS | 2003年 / 40卷 / 08期

关键词：

D O I：

10.1136/jmg.40.8.e99

中图分类号：

Q3 [遗传学];

学科分类号：

071007 ; 090102 ;

摘要：

[No abstract available]

引用

页数：5

共 32 条

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