THE PRADER-WILLI SYNDROME AND INTERSTITIAL DELETION OF CHROMOSOME 15 - HIGH-RESOLUTION CHROMOSOME ANALYSES OF 14 PATIENTS WITH THE PRADER-WILLI SYNDROME AND OF 5 SUSPECTED INFANTS

被引：8

作者：

FUKUSHIMA, Y ^{[1
]}

NIIKAWA, N ^{[1
]}

KUROKI, Y ^{[1
]}

机构：

[1] HOKKAIDO UNIV,SCH MED,DEPT PEDIAT,KITA KU,SAPPORO,HOKKAIDO 060,JAPAN

来源：

JAPANESE JOURNAL OF HUMAN GENETICS | 1984年 / 29卷 / 01期

关键词：

D O I：

10.1007/BF01876751

中图分类号：

Q3 [遗传学];

学科分类号：

071007 ; 090102 ;

摘要：

引用

页码：1 / 6

页数：6

共 7 条

[1] Holm V. A., 1981, PRADERWILLI SYNDROME, P27
[2] ACCUMULATION OF EARLY MITOTIC CELLS IN ETHIDIUM BROMIDE-TREATED HUMAN LYMPHOCYTE-CULTURES
IKEUCHI, T
SASAKI, M
[J]. PROCEEDINGS OF THE JAPAN ACADEMY SERIES B-PHYSICAL AND BIOLOGICAL SCIENCES, 1979, 55 (01): : 15 - 18
[3] THE CYTOGENETIC CONTROVERSY IN THE PRADER-LABHART-WILLI SYNDROME
KOUSSEFF, BG
[J]. AMERICAN JOURNAL OF MEDICAL GENETICS, 1982, 13 (04): : 431 - 439
[4] LEDBETTER DH, 1982, AM J HUM GENET, V34, P278
[5] DELETIONS OF CHROMOSOME-15 AS A CAUSE OF THE PRADER-WILLI SYNDROME
LEDBETTER, DH
RICCARDI, VM
AIRHART, SD
STROBEL, RJ
KEENAN, BS
CRAWFORD, JD
[J]. NEW ENGLAND JOURNAL OF MEDICINE, 1981, 304 (06) : 325 - 329
[6] MCKUSICK VA, 1978, MENDERIAN INHERITANC, P644
[7] 1981, CYTOGENET CELL GENET, V31, P1