PARTIAL MONOSOMY 3Q IN A BOY WITH SHORT STATURE, DEVELOPMENTAL DELAY, AND MILD DYSMORPHIC FEATURES

被引：16

作者：

BRUETON, LA

BARBER, JCK

HUSON, SM

WINTER, RM

机构：

来源：

JOURNAL OF MEDICAL GENETICS | 1989年 / 26卷 / 11期

关键词：

D O I：

10.1136/jmg.26.11.729

中图分类号：

Q3 [遗传学];

学科分类号：

071007 ; 090102 ;

摘要：

引用

收藏

页码：729 / 730

页数：2

相关论文

共 5 条

[1] ARRATIA MCA, 1984, ANN GENET-PARIS, V27, P109
[2] INTERSTITIAL DELETION OF THE LONG ARM OF CHROMOSOME-3 IN A PATIENT WITH MENTAL-RETARDATION AND CONGENITAL-ANOMALIES
FRANCESCHINI, P
SILENGO, MC
DAVI, G
BIANCO, R
BIAGIOLI, M
[J]. HUMAN GENETICS, 1983, 64 (01) : 97 - 97
[3] MARTSOLF JT, 1983, ANN GENET-PARIS, V26, P98
[4] TRIGONOCEPHALY AND THE OPITZ C-SYNDROME
SARGENT, C
BURN, J
BARAITSER, M
PEMBREY, ME
[J]. JOURNAL OF MEDICAL GENETICS, 1985, 22 (01) : 39 - 45
[5] FAMILIAL INSERTIONAL TRANSLOCATION OF A PORTION OF 3Q INTO 11Q RESULTING IN DUPLICATION AND DELETION OF REGION 3Q22.1-]Q24 IN DIFFERENT OFFSPRING
WILLIAMSON, RA
DONLAN, MA
DOLAN, CR
THULINE, HC
HARRISON, MT
HALL, JG
[J]. AMERICAN JOURNAL OF MEDICAL GENETICS, 1981, 9 (02): : 105 - 111