A TAXONOMIC APPROACH TO THE DEL(4P) PHENOTYPE

被引:26
作者
PREUS, M
AYME, S
KAPLAN, P
VEKEMANS, M
机构
[1] MONTREAL CHILDRENS HOSP,DIV MED GENET,MONTREAL H3H 1P3,QUEBEC,CANADA
[2] MEM UNIV NEWFOUNDLAND,FAC MED,ST JOHNS A1C 5S7,NEWFOUNDLAND,CANADA
[3] HOP ENFANTS TIMONE,CTR GENET MED,INSERM,U242,F-13385 MARSEILLE 4,FRANCE
[4] MONTREAL CHILDRENS HOSP,DIV MED GENET,MONTREAL H3H 1P3,QUEBEC,CANADA
来源
AMERICAN JOURNAL OF MEDICAL GENETICS | 1985年 / 21卷 / 02期
关键词
D O I
10.1002/ajmg.1320210216
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
引用
收藏
页码:337 / 345
页数:9
相关论文
共 12 条
[1]   HUMAN CHROMOSOMAL DELETION . 2 PATIENTS WITH 4P-SYNDROME [J].
ARIAS, D ;
PASSARGE, E ;
ENGLE, MA ;
GERMAN, J .
JOURNAL OF PEDIATRICS, 1970, 76 (01) :82-+
[3]  
BUNDEY S, 1974, J MENT DEFIC RES, V18, P51
[4]  
CURRY CJR, 1982, BIRTH DEFECTS-ORIG, V18, P275
[5]  
HANNIG V, 1984, P GREENWOOD GENET CT, V3, P19
[6]  
LINDSLEY DL, 1972, GENETICS, V71, P157
[7]   4P- PHENOTYPE IN AN INFANT WITH T(4P-19P OR Q+)MAT TRANSLOCATION [J].
NEU, RL ;
SHOTT, RJ ;
GARDNER, LI .
AMERICAN JOURNAL OF DISEASES OF CHILDREN, 1975, 129 (03) :363-365
[8]  
PREUS M, 1983, CLIN GENET, V23, P1
[9]  
Schinzel A, 1984, CATALOGUE UNBALANCED
[10]  
STENGELRUTKOWSKI S, 1984, CLIN GENET, V25, P500