Detection of i(12p) in lymphocytes in Pallister-Killian syndrome (PKS). Clinical similarities with Fryns Syndrome (FS) and implications on counseling.

被引：0
|
作者：
Furforo, L
Rittler, M
Sponsa, S
Slavutsky, I
机构：
[1] Hosp Materno Infantil Ramon Sarda, Secc Genet Med, Buenos Aires, DF, Argentina
[2] Acad Nacl Med, Inst Invest Hematol, Dept Genet, Buenos Aires, DF, Argentina
来源：
AMERICAN JOURNAL OF HUMAN GENETICS | 1997年 / 61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：
709
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收藏
页码：A125 / A125
页数：1
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