FAMILIAL PARTIAL 7Q MONOSOMY RESULTING FROM SEGREGATION OF AN INSERTIONAL CHROMOSOME REARRANGEMENT

被引:21
作者
NIELSEN, KB
MOURIDSEN, FEI
MOHR, J
机构
[1] NAESTVED HOSP,DEPT PAEDIAT,NAESTVED,DENMARK
[2] ANDERSVAENGE,INST MENTALLY RETARDED,SLAGELSE,DENMARK
[3] UNIV COPENHAGEN,INST HUMAN GENET,COPENHAGEN,DENMARK
关键词
D O I
10.1136/jmg.16.6.461
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
A family with an insertional type of chromosome rearrangement involving chromosomes 7 and 13 is reported. An interstitial deletion of a segment of chromosome 7 (7q32→34) had been inserted into the long arm of chromosome 13 at breakpoint q32. Segregation of this chromosome rearrangement gave rise to three subjects who were monosomic for the involved segment of chromosome 7. The karyotypes were: 46,XX, or XY,der(7)ins(13;7) (q32;q32q34). All three subjects were mentally retarded and had minor dysmorphic features. The Kidd, Colton, and Kell blood group systems were investigated, but were not informative.
引用
收藏
页码:461 / 466
页数:6
相关论文
共 21 条
[1]  
AYRAUD N, 1976, ANN GENET-PARIS, V19, P265
[2]   2 DIFFERENT CHROMOSOME ABNORMALITIES RESULTING FROM A TRANSLOCATION CARRIER FATHER [J].
BASS, HN ;
CRANDALL, BF ;
MARCY, SM .
JOURNAL OF PEDIATRICS, 1973, 83 (06) :1034-1038
[3]  
BIEDERMAN B, 1978, HUM GENET, V41, P101
[4]  
CHAPELLE ADL, 1975, LANCET, V2, P817
[5]   FAMILIAL MENTAL-RETARDATION IN A FAMILY WITH AN INHERITED CHROMOSOME REARRANGEMENT [J].
CHUDLEY, AE ;
BAUDER, F ;
RAY, M ;
MCALPINE, PJ ;
PENA, SDJ ;
HAMERTON, JL .
JOURNAL OF MEDICAL GENETICS, 1974, 11 (04) :353-366
[6]   A CASE OF 6P- CHROMOSOMAL ABERRATION [J].
DEGROUCH.J ;
VESLOT, J ;
BONNETTE, J ;
ROIDOT, M .
AMERICAN JOURNAL OF DISEASES OF CHILDREN, 1968, 115 (01) :93-+
[7]  
DEGROUCHY J, 1974, HUMANGENETIK, V24, P197
[8]  
DINNO N, 1977, BIRTH DEFECTS OAS, V13, P228
[9]   INTERSTITIAL DELETION OF LONG ARM OF CHROMOSOME 746,XX,DEL(7)(PTER-]Q2200-Q3200-]QTER) [J].
FRANCESCHINI, P ;
SILENGO, MC ;
DAVI, GF ;
SANTORO, MA ;
PRANDI, G ;
FABRIS, C .
HUMAN GENETICS, 1978, 44 (03) :345-348
[10]  
HARRIS EL, 1977, CLIN GENET, V12, P233