IDENTICAL MULTIPLE CONGENITAL-ANOMALIES MENTAL-RETARDATION (MCA/MR) SYNDROME DUE TO DEL(2)(Q32) IN 2 SISTERS WITH INTRACHROMOSOMAL INSERTIONAL TRANSLOCATION IN THEIR FATHER

被引:29
作者
PAI, GS
ROGERS, JF
SOMMER, A
机构
[1] MED UNIV S CAROLINA,DEPT PATHOL,CHARLESTON,SC 29425
[2] OHIO STATE UNIV,COLL MED,DEPT PEDIAT,COLUMBUS,OH 43210
[3] CHILDRENS HOSP,DIV GENET,COLUMBUS,OH 43205
来源
AMERICAN JOURNAL OF MEDICAL GENETICS | 1983年 / 14卷 / 01期
关键词
D O I
10.1002/ajmg.1320140125
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
引用
收藏
页码:189 / 195
页数:7
相关论文
共 19 条
[1]  
ALLDERDICE PW, 1981, AM J HUM GENET, V33, pA70
[2]  
CARR DH, 1971, ADV HUM GENET, P201
[3]  
GARVER KL, 1976, CLIN GENET, V10, P319
[4]  
GRASS FS, 1981, CLIN GENET, V20, P28
[5]  
HULTEN M, 1974, HEREDITAS, V76, P55
[6]  
JACOBS PA, 1978, CLIN GENET, V13, P37
[7]  
JACOBS PA, 1977, POPULATION CYTOGENET, P81
[8]  
KAJII T, 1973, AM J HUM GENET, V25, P539
[9]  
LAURITSEN JG, 1976, ACTA OBSTET GYNECO S, V52, P3
[10]   PARTIAL DELETION OF CHROMOSOME-2 MIMICKING A PHENOTYPE OF TRISOMY-18 - CASE-REPORT WITH AUTOPSY [J].
MCCONNELL, TS ;
KORNFELD, M ;
MCCLELLAN, G ;
AASE, J .
HUMAN PATHOLOGY, 1980, 11 (02) :202-205