CHROMOSOME-15 IN FLOPPY INFANTS

被引：22

作者：

BERRY, AC ^{[1
]}

WHITTINGHAM, AJ ^{[1
]}

NEVILLE, BGR ^{[1
]}

机构：

[1] GUYS HOSP,SCH MED,NEWCOMEN CTR,LONDON SE1 9RT,ENGLAND

来源：

ARCHIVES OF DISEASE IN CHILDHOOD | 1981年 / 56卷 / 11期

关键词：

D O I：

10.1136/adc.56.11.882

中图分类号：

R72 [儿科学];

学科分类号：

100202 ;

摘要：

引用

收藏

页码：882 / 885

页数：4

相关论文

共 10 条

[1] BARTSCHSANDHOFF M, 1977, LANCET, V1, P551
[2] EMBERGER JM, 1977, ANN GENET-PARIS, V20, P297
[3] 15/15 TRANSLOCATION IN PRADER-WILLI SYNDROME
FRACCARO, M
ZUFFARDI, O
BUHLER, EM
JURIK, LP
[J]. JOURNAL OF MEDICAL GENETICS, 1977, 14 (04) : 275 - 276
[4] PRADER-WILLI SYNDROME WITH A 15-15 TRANSLOCATION
HAWKEY, CJ
SMITHIES, A
[J]. JOURNAL OF MEDICAL GENETICS, 1976, 13 (02) : 152 - 157
[5] PRADER-WILLI SYNDROME WITH A 15-3 TRANSLOCATION
KUCEROVA, M
STRAKOVA, M
POLIVKOVA, Z
[J]. JOURNAL OF MEDICAL GENETICS, 1979, 16 (03) : 234 - 235
[6] 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
[7] LEJEUNE J, 1979, ANN GENET-PARIS, V22, P210
[8] A GIRL WITH THE PRADER-WILLI SYNDROME AND ROBERTSONIAN TRANSLOCATION 45,XX,T(14-15)(P11-Q11) WHICH WAS PRESENT IN 3 NORMAL FAMILY MEMBERS
SMITH, A
NOEL, M
[J]. HUMAN GENETICS, 1980, 55 (02) : 271 - 273
[9] ROBERTSONIAN TRANSLOCATION BETWEEN CHROMOSOME Y AND 15
SUBRT, I
BLEHOVA, B
[J]. HUMANGENETIK, 1974, 23 (04): : 305 - 309
[10] WISNIEWSKI LP, 1980, CLIN GENET, V18, P42