Diagnostic testing for Prader-Willi and Angelman syndromes: Response

被引：0

作者：

Smith, A

Buchholz, T

Robson, L

机构：

来源：

AMERICAN JOURNAL OF HUMAN GENETICS | 1997年 / 61卷 / 01期

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D O I：

暂无

中图分类号：

Q3 [遗传学];

学科分类号：

071007 ; 090102 ;

摘要：

引用

页码：241 / 244

页数：4

共 12 条

[1]

*AM SOC HUM GEN AM, 1996, AM J HUM GENET, V58, P1085

[2] DIAGNOSIS IN PRADER-WILLI-SYNDROME [J].

CHU, CE ;

COOKE, A ;

STEPHENSON, JBP ;

TOLMIE, JL ;

CLARKE, B ;

PARRYJONES, WL ;

CONNOR, JM ;

DONALDSON, MDC .

ARCHIVES OF DISEASE IN CHILDHOOD, 1994, 71 (05) :441-442

[3]

DITTRICH B, 1992, HUM GENET, V90, P313

[4]

Erdel M, 1996, HUM GENET, V97, P784

[5]

HOLM VA, 1993, PEDIATRICS, V91, P398

[6]

Kubota T, 1996, AM J MED GENET, V66, P77, DOI 10.1002/(SICI)1096-8628(19961202)66:1<77::AID-AJMG18>3.0.CO

[7]

2-N

[8] A SIMPLE SALTING OUT PROCEDURE FOR EXTRACTING DNA FROM HUMAN NUCLEATED CELLS [J].

MILLER, SA ;

DYKES, DD ;

POLESKY, HF .

NUCLEIC ACIDS RESEARCH, 1988, 16 (03) :1215-1215

[9]

Monaghan KG, 1997, AM J HUM GENET, V60, P244

[10] COMPARISON OF HIGH-RESOLUTION CYTOGENETICS, FLUORESCENCE IN-SITU HYBRIDIZATION, AND DNA STUDIES TO VALIDATE THE DIAGNOSIS OF PRADER-WILLI AND ANGELMANS SYNDROMES [J].

SMITH, A ;

PRASAD, M ;

DENG, ZM ;

ROBSON, L ;

WOODAGE, T ;

TRENT, RJ .

ARCHIVES OF DISEASE IN CHILDHOOD, 1995, 72 (05) :397-402

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