ABSENCE OF EXCESS CHROMOSOME BREAKAGE IN A PATIENT WITH VACTERL-HYDROCEPHALUS

被引：9

作者：

EVANS, JA

CHODIRKER, BN

机构：

[1] CHILDRENS HOSP,WINNIPEG,MB,CANADA

[2] UNIV MANITOBA,DEPT PEDIAT,WINNIPEG R3T 2N2,MANITOBA,CANADA

[3] UNIV MANITOBA,DEPT CHILD HLTH,WINNIPEG R3T 2N2,MANITOBA,CANADA

来源：

AMERICAN JOURNAL OF MEDICAL GENETICS | 1993年 / 47卷 / 01期

关键词：

D O I：

10.1002/ajmg.1320470123

中图分类号：

Q3 [遗传学];

学科分类号：

071007 ; 090102 ;

摘要：

引用

页码：112 / 113

页数：2

共 6 条

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EVANS, JA
STRANC, LC
KAPLAN, P
HUNTER, AGW
[J]. AMERICAN JOURNAL OF MEDICAL GENETICS, 1989, 34 (02): : 177 - 182
[2] VATER AND HYDROCEPHALUS - DISTINCT SYNDROME
IAFOLLA, AK
MCCONKIEROSELL, A
CHEN, YT
[J]. AMERICAN JOURNAL OF MEDICAL GENETICS, 1991, 38 (01): : 46 - 51
[3] NERI G, 1991, 2ND INT WORKSH FET G
[4] VACTERL WITH HYDROCEPHALUS - ONE END OF THE FANCONI ANEMIA SPECTRUM OF ANOMALIES
PORTEOUS, MEM
CROSS, I
BURN, J
[J]. AMERICAN JOURNAL OF MEDICAL GENETICS, 1992, 43 (06): : 1032 - 1034
[5] SOMMER A, 1989, P GREENWOOD GENET CT, V8, P188
[6] TORIELLO HV, 1992, P GREENWOOD GENET CT, V11, P142