PRADER-WILLI SYNDROME WITH A 15-15 TRANSLOCATION

被引：85
作者：
HAWKEY, CJ
SMITHIES, A
机构：
[1] NORTHWICK PK HOSP, HARROW, MIDDLESEX, ENGLAND
[2] CLIN RES CTR, HARROW, MIDDLESEX, ENGLAND
来源：
JOURNAL OF MEDICAL GENETICS | 1976年 / 13卷 / 02期
关键词：
D O I：
10.1136/jmg.13.2.152
中图分类号：
Q3 [遗传学];
学科分类号：
071007 ; 090102 ;
摘要：
引用
收藏
页码：152 / 157
页数：6
相关论文
共 32 条
[1]   PATHOLOGY OF MUSCULAR HYPOTONIA IN PRADER-WILLI SYNDROME LIGHT AND ELECTRON MICROSCOPIC STUDY [J].
AFIFI, AK ;
ZELLWEGE.H .
JOURNAL OF THE NEUROLOGICAL SCIENCES, 1969, 9 (01) :49-&
[2]   PERSISTENT HYPERNATREMIA DUE TO ABNORMAL THIRST MECHANISM IN A 13-YEAR-OLD CHILD WITH NEPHROGENIC DIABETES-INSIPIDUS [J].
ANAND, SK ;
KOGUT, MD ;
LIEBERMAN, E .
JOURNAL OF PEDIATRICS, 1972, 81 (06) :1097-+
[3]   CHROMOSOMAL TRANSLOCATION IN A MENTALLY DEFICIENT CHILD WITH CRYPTORCHIDISM [J].
BUHLER, EM ;
ROSSIER, R ;
STALDER, G ;
BUHLER, UK ;
VULLIET, V ;
BODIS, I .
ACTA PAEDIATRICA, 1963, 52 (02) :177-&
[4]   PRADER-WILLI SYNDROME [J].
COHEN, MM ;
GORLIN, RJ .
AMERICAN JOURNAL OF DISEASES OF CHILDREN, 1969, 117 (02) :213-+
[5]  
COURTBROWN WM, 1967, HUMAN POPULATION CYT
[6]   A SYNDROME OF BENIGN CONGENITAL HYPOTONIA GROSS OBESITY DELAYED INTELLECTUAL DEVELOPMENT RETARDED BONE AGE AND UNUSUAL FACIES [J].
DUBOWITZ, V .
PROCEEDINGS OF THE ROYAL SOCIETY OF MEDICINE-LONDON, 1967, 60 (10) :1006-&
[7]  
DUNN HG, 1968, ACTA PAEDIATR SCAND, VS, P1
[8]  
DUNN HG, 1961, PEDIATRICS, V28, P578
[9]  
EVANS P. R., 1964, GUY S HOSP REP, V113, P207
[10]   PRADER-WILLI SYNDROME IN BOY OF 10 WITH PREDIABETES [J].
FORSSMAN, H ;
HAGBERG, B .
ACTA PAEDIATRICA, 1964, 53 (01) :70-&
1234