Breakpoint mapping of an apparently balanced 2;8 translocation reveals a cryptic deletion on 2q in a child with autism.

被引：0
作者：
Borg, I
Stout, K
Sargan, DR
Morgan, D
Willatt, L
Kalscheuer, V
Tommerup, N
Ropers, HH
Ferguson-Smith, MA
机构：
[1] Univ Cambridge, Dept Clin Vet Med, Cambridge CB3 0ES, England
[2] Addenbrookes NHS Trust, Dept Med Genet, Cambridge, England
[3] Max Planck Inst Mol Genet, Berlin, Germany
[4] Addenbrookes NHS Trust, Cytogenetics Lab, Cambridge CB2 2QQ, England
[5] IMBG, Dept Med Genet, Copenhagen, Denmark
来源：
AMERICAN JOURNAL OF HUMAN GENETICS | 2000年 / 67卷 / 04期
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D O I：
暂无
中图分类号：
Q3 [遗传学];
学科分类号：
071007 ; 090102 ;
摘要：
836
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收藏
页码：159 / 159
页数：1
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