CLINICAL FINDINGS IN PATIENTS WITH MARKER CHROMOSOMES IDENTIFIED BY FLUORESCENCE IN-SITU HYBRIDIZATION

被引：0
|
作者：
PLATTNER, R
HEEREMA, NA
HOWARDPEEBLES, PN
MILES, JH
SOUKUP, S
PALMER, CG
机构：
[1] INDIANA UNIV,SCH MED,DEPT MED & MOLEC GENET,975 W WALNUT ST,INDIANAPOLIS,IN 46202
[2] GENET & IVF INST,FAIRFAX,VA 22031
[3] VIRGINIA COMMONWEALTH UNIV,MED COLL VIRGINIA,DEPT HUMAN GENET,RICHMOND,VA 23298
[4] UNIV CINCINNATI,CHILDRENS HOSP,MED CTR,COLL MED,DEPT PEDIAT,CINCINNATI,OH 45221
[5] UNIV MISSOURI,MED CTR,DEPT MED GENET,COLUMBIA,MO 65201
来源：
HUMAN GENETICS | 1993年 / 91卷 / 06期
关键词：
D O I：
暂无
中图分类号：
Q3 [遗传学];
学科分类号：
071007 ; 090102 ;
摘要：
Twenty-seven patients carrying marker chromosomes were previously collected, characterized by cytogenetic techniques, and identified by stepwise fluorescence in situ hybridization (FISH) with alpha-satellite DNA probes. Clinical features of 22 patients are described here and compared to other patients with marker chromosomes similarly identified and reported in the literature.
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页码：589 / 598
页数：10
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