A newly recognised microdeletion syndrome involving 2p15p16.1: narrowing down the critical region by adding another patient detected by genome wide tiling path array comparative genomic hybridisation analysis

被引：40

作者：

De Leeuw, N. ^{[1
]}

Pfundt, R. ^{[1
]}

Koolen, D. A. ^{[1
]}

Neefs, I. ^{[1
]}

Scheltinga, I. ^{[1
]}

Mieloo, H. ^{[1
]}

Sistermans, E. A. ^{[2
]}

Nillesen, W. ^{[1
]}

Smeets, D. F. ^{[1
]}

de Vries, B. B. A. ^{[1
]}

Knoers, N. V. A. M. ^{[1
]}

机构：

[1] Radboud Univ Nijmegen, Med Ctr, Dept Human Genet, NL-6500 HB Nijmegen, Netherlands

[2] Vrije Univ Amsterdam, Med Ctr, Dept Clin Genet, Amsterdam, Netherlands

来源：

JOURNAL OF MEDICAL GENETICS | 2008年 / 45卷 / 02期

关键词：

D O I：

10.1136/jmg.2007.054049

中图分类号：

Q3 [遗传学];

学科分类号：

071007 ; 090102 ;

摘要：

引用

页码：122 / 124

页数：3

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