Novel PHF6 mutation p.D333del causes Borjeson-Forssman-Lehmann syndrome -: art. no. e50

被引：25

作者：

Baumstark, A

Lower, KM

Sinkus, A

Andriuskeviciute, I

Jurkeniene, L

Gécz, J

Just, W

机构：

[1] Univ Ulm, Abt Humangenet, D-89081 Ulm, Germany

[2] Womens & Childrens Hosp, Dept Lab Genet, Neurogenet Lab, Adelaide, SA 5006, Australia

[3] Univ Adelaide, Dept Paediat, Adelaide, SA, Australia

[4] Kaunas Univ Med, Dept Biol, Lab Cytogenet, LT-3000 Kaunas, Lithuania

来源：

JOURNAL OF MEDICAL GENETICS | 2003年 / 40卷 / 04期

关键词：

D O I：

10.1136/jmg.40.4.e50

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：6

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