CONGENITAL DIAPHRAGMATIC-HERNIA, COARSE FACIES, AND ACRAL HYPOPLASIA - FRYNS SYNDROME

被引：55

作者：

BAMFORTH, JS

LEONARD, CO

CHODIRKER, BN

CHITAYAT, D

GRITTER, HL

EVANS, JA

KEENA, B

PANTZAR, T

FRIEDMAN, JM

HALL, JG

机构：

[1] UNIV BRITISH COLUMBIA, DEPT MED GENET, WESTBROOK BLDG, VANCOUVER V6T 1W5, BC, CANADA

[2] CHILDRENS HOSP, DEPT PATHOL, DIV CYTOGENET, VANCOUVER, BC, CANADA

[3] UNIV UTAH, MED CTR, DEPT PEDIAT, MED GENET PROGRAM, SALT LAKE CITY, UT 84112 USA

[4] UNIV MANITOBA, DEPT PEDIAT & CHILD HLTH, WINNIPEG R3T 2N2, MANITOBA, CANADA

[5] UNIV MANITOBA, DEPT HUMAN GENET, WINNIPEG R3T 2N2, MANITOBA, CANADA

[6] UNIV MANITOBA, DEPT PATHOL, WINNIPEG R3T 2N2, MANITOBA, CANADA

来源：

AMERICAN JOURNAL OF MEDICAL GENETICS | 1989年 / 32卷 / 01期

关键词：

D O I：

10.1002/ajmg.1320320120

中图分类号：

Q3 [遗传学];

学科分类号：

071007 ; 090102 ;

摘要：

引用

页码：93 / 99

页数：7

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