Are sequence family variants useful for identifying deletions in the human Y chromosome?

被引：19
作者：
Repping, S
Korver, CM
Oates, RD
Silber, S
van der Veen, F
Page, DC
Rozen, S
机构：
[1] Whitehead Inst, Howard Hughes Med Inst, Cambridge, MA 02142 USA
[2] MIT, Dept Biol, Cambridge, MA 02139 USA
[3] Univ Amsterdam, Acad Med Ctr, Dept Obstet & Gynecol, Ctr Reprod Med, NL-1105 AZ Amsterdam, Netherlands
[4] Boston Univ, Med Ctr, Dept Urol, Boston, MA USA
[5] St Lukes Hosp, Infertil Ctr St Louis, St Louis, MO USA
来源：
AMERICAN JOURNAL OF HUMAN GENETICS | 2004年 / 75卷 / 03期
关键词：
D O I：
10.1086/423394
中图分类号：
Q3 [遗传学];
学科分类号：
071007 ; 090102 ;
摘要：
引用
收藏
页码：514 / 517
页数：4
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