SIMILAR MOLECULAR DELETIONS ON CHROMOSOME 15Q11.2 ARE ENCOUNTERED IN BOTH THE PRADER-WILLI AND ANGELMAN SYNDROMES

被引:92
作者
DONLON, TA [1 ]
机构
[1] STANFORD UNIV,MED CTR,SCH MED,DEPT PATHOL,STANFORD,CA 94305
关键词
D O I
10.1007/BF00273644
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
引用
收藏
页码:322 / 328
页数:7
相关论文
共 52 条
[1]  
ALDRIDGE J, 1984, AM J HUM GENET, V36, P546
[2]   GENE-MAPPING WITHIN THE T/T COMPLEX OF THE MOUSE .2. ANOMALOUS POSITION OF THE H-2-COMPLEX IN T-HAPLOTYPES [J].
ARTZT, K ;
SHIN, HS ;
BENNETT, D .
CELL, 1982, 28 (03) :471-476
[3]  
BARAITSER M, 1987, CLIN GENET, V31, P323
[4]  
BROOKWELL R, 1987, CLIN GENET, V31, P311
[5]   44 PROBANDS WITH AN ADDITIONAL MARKER CHROMOSOME [J].
BUCKTON, KE ;
SPOWART, G ;
NEWTON, MS ;
EVANS, HJ .
HUMAN GENETICS, 1985, 69 (04) :353-370
[6]   FAMILIAL PRADER-WILLI SYNDROME [J].
BURKE, CM ;
KOUSSEFF, BG ;
GLEESON, M ;
OCONNELL, BM ;
DEVLIN, JG .
ARCHIVES OF INTERNAL MEDICINE, 1987, 147 (04) :673-675
[7]   CLINICAL AND CYTOGENETIC SURVEY OF 39 INDIVIDUALS WITH PRADER-LABHART-WILLI SYNDROME [J].
BUTLER, MG ;
MEANEY, FJ ;
PALMER, CG .
AMERICAN JOURNAL OF MEDICAL GENETICS, 1986, 23 (03) :793-809
[8]   ACROCEPHALOPOLYSYNDACTYLY TYPE-II - CARPENTER SYNDROME - CLINICAL SPECTRUM AND AN ATTEMPT AT UNIFICATION WITH GOODMAN AND SUMMIT SYNDROMES [J].
COHEN, DM ;
GREEN, JG ;
MILLER, J ;
GORLIN, RJ ;
REED, JA .
AMERICAN JOURNAL OF MEDICAL GENETICS, 1987, 28 (02) :311-324
[9]  
COHEN MM, 1973, J PEDIATR-US, V83, P280
[10]  
DEFRANCE HF, 1984, CLIN GENET, V26, P379