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
收藏
页码：112 / 113
页数：2
相关论文
共 6 条
[1]   VACTERL WITH HYDROCEPHALUS - FURTHER DELINEATION OF THE SYNDROME(S) [J].
EVANS, JA ;
STRANC, LC ;
KAPLAN, P ;
HUNTER, AGW .
AMERICAN JOURNAL OF MEDICAL GENETICS, 1989, 34 (02) :177-182
[2]   VATER AND HYDROCEPHALUS - DISTINCT SYNDROME [J].
IAFOLLA, AK ;
MCCONKIEROSELL, A ;
CHEN, YT .
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 [J].
PORTEOUS, MEM ;
CROSS, I ;
BURN, 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
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