FOREBRAIN CLEAVAGE GENE CAUSING HOLOPROSENCEPHALY - DELETION MAPPING TO CHROMOSOME BAND 2P21

被引：10

作者：

HECHT, BK

HECHT, F

MUNKE, M

机构：

[1] CHILDRENS HOSP,DIV HUMAN GENET & MOLEC BIOL,PHILADELPHIA,PA 19104

[2] CHILDRENS MERCY HOSP,DIV MOLEC MED,KANSAS CITY,MO 64108

来源：

AMERICAN JOURNAL OF MEDICAL GENETICS | 1991年 / 40卷 / 01期

关键词：

D O I：

10.1002/ajmg.1320400131

中图分类号：

Q3 [遗传学];

学科分类号：

071007 ; 090102 ;

摘要：

引用

页码：130 / 130

页数：1

共 8 条

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NIEMEYER, P ;

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WARD, VF ;

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[3]

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[4]

HECHT F, 1980, 18TH ANN SOM CELL GE

[5] HOLOPROSENCEPHALY - ASSOCIATION WITH INTERSTITIAL DELETION OF 2P AND REVIEW OF THE CYTOGENETIC LITERATURE [J].

MUNKE, M ;

EMANUEL, BS ;

ZACKAI, EH .

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[6] CLINICAL, CYTOGENETIC, AND MOLECULAR APPROACHES TO THE GENETIC-HETEROGENEITY OF HOLOPROSENCEPHALY [J].

MUNKE, M .

AMERICAN JOURNAL OF MEDICAL GENETICS, 1989, 34 (02) :237-245

[7]

SHANKS DE, AM J HUM GENET, V43, pA122

[8]

WILSON WG, 1989, AM J MED GENET, V32, P252

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