IS ANGELMAN SYNDROME AN ALTERNATE RESULT OF DEL(15)(Q11Q13)

被引：183

作者：

MAGENIS, RE

BROWN, MG

LACY, DA

BUDDEN, S

LAFRANCHI, S

机构：

[1] OREGON HLTH SCI UNIV,CTR CHILD DEV & REHABIL,DEPT PEDIAT,PORTLAND,OR 97201

[2] OREGON HLTH SCI UNIV HOSP,PORTLAND,OR 97201

来源：

AMERICAN JOURNAL OF MEDICAL GENETICS | 1987年 / 28卷 / 04期

关键词：

D O I：

10.1002/ajmg.1320280407

中图分类号：

Q3 [遗传学];

学科分类号：

071007 ; 090102 ;

摘要：

引用

页码：829 / 838

页数：10

共 18 条

[1]

ANGELMAN H, 1965, DEV MED CHILD NEUROL, V7, P681

[2] ISOLATION OF MOLECULAR PROBES ASSOCIATED WITH THE CHROMOSOME-15 INSTABILITY IN THE PRADER-WILLI SYNDROME [J].

DONLON, TA ;

LALANDE, M ;

WYMAN, A ;

BRUNS, G ;

LATT, SA .

PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1986, 83 (12) :4408-4412

[3] THE PUPPET-LIKE SYNDROME OF ANGELMAN [J].

DOOLEY, JM ;

BERG, JM ;

PAKULA, Z ;

MACGREGOR, DL .

AMERICAN JOURNAL OF DISEASES OF CHILDREN, 1981, 135 (07) :621-624

[4] INSITU HYBRIDIZATION AND TRANSLOCATION BREAKPOINT MAPPING .1. NONIDENTICAL 22Q11 BREAKPOINTS FOR THE T(9-22) OF CML AND THE T(8-22) OF BURKITT-LYMPHOMA [J].

EMANUAL, BS ;

SELDEN, JR ;

WANG, E ;

NOWELL, PC ;

CROCE, CM .

CYTOGENETICS AND CELL GENETICS, 1984, 38 (02) :127-131

[5]

EMBERGER JM, 1977, ANN GENET-PARIS, V20, P297

[6] QUANTITATIVE-ANALYSIS OF HIGH-RESOLUTION TRYPSIN-GIEMSA BANDS ON HUMAN PROMETAPHASE CHROMOSOMES [J].

FRANCKE, U ;

OLIVER, N .

HUMAN GENETICS, 1978, 45 (02) :137-165

[7] DELETIONS OF PROXIMAL 15Q WITHOUT PRADER-WILLI SYNDROME [J].

GREENBERG, F ;

LEDBETTER, DH .

AMERICAN JOURNAL OF MEDICAL GENETICS, 1987, 28 (04) :813-820

[8]

HAWKEY CJ, 1976, J MED GENET, V14, P275

[9]

KAPLAN LC, 1987, IN PRESS AM J MED GE

[10]

LEDBETTER DH, 1982, AM J HUM GENET, V34, P278

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