DELETION OF CHROMOSOME-15 (Q11-13) IN A PRADER-LABHART-WILLI SYNDROME CLINIC POPULATION

被引：45

作者：

CASSIDY, SB

THULINE, HC

HOLM, VA

机构：

[1] UNIV WASHINGTON,CTR CHILD DEV & MENTAL RETARDAT,DEPT PEDIAT,SEATTLE,WA 98195

[2] UNIV WASHINGTON,CTR CHILD DEV & MENTAL RETARDAT,CLIN TRAINING UNIT,SEATTLE,WA 98195

[3] WASHINGTON STATE DEPT SOCIAL & HLTH SERV,GENET PROGRAM CYTOGENET LAB,SEATTLE,WA

来源：

AMERICAN JOURNAL OF MEDICAL GENETICS | 1984年 / 17卷 / 02期

关键词：

D O I：

10.1002/ajmg.1320170211

中图分类号：

Q3 [遗传学];

学科分类号：

071007 ; 090102 ;

摘要：

引用

页码：485 / 495

页数：11

共 22 条

[1] BUTLER MG, 1983, LANCET, V1, P1285
[2] CASSIDY SB, 1981, CLIN RES, V29, pA114
[3] PRADER-WILLI SYNDROME - VARIABLE SEVERITY AND RECURRENCE RISK
CLARREN, SK
SMITH, DW
[J]. AMERICAN JOURNAL OF DISEASES OF CHILDREN, 1977, 131 (07): : 798 - 800
[4] PRADER-WILLI SYNDROME - RESUME OF 32 CASES INCLUDING AN INSTANCE OF AFFECTED FIRST COUSINS, ONE OF WHOM IS OF NORMAL STATURE AND INTELLIGENCE
HALL, BD
SMITH, DW
[J]. JOURNAL OF PEDIATRICS, 1972, 81 (02) : 286 - +
[5] PRADER-WILLI SYNDROME WITH A 15-15 TRANSLOCATION
HAWKEY, CJ
SMITHIES, A
[J]. JOURNAL OF MEDICAL GENETICS, 1976, 13 (02) : 152 - 157
[6] Holm V. A., 1981, PRADERWILLI SYNDROME, P27
[7] HOLM VA, 1981, DEV MED CHILD NEUROL, V23, P192
[8] HOOK EB, 1977, AM J HUM GENET, V29, P94
[9] THE CYTOGENETIC CONTROVERSY IN THE PRADER-LABHART-WILLI SYNDROME
KOUSSEFF, BG
[J]. AMERICAN JOURNAL OF MEDICAL GENETICS, 1982, 13 (04): : 431 - 439
[10] KOUSSEFF BG, 1982, BIRTH DEFECTS-ORIG, V18, P301