Inter- and intrachromosomal rearrangements are both involved in the origin of 15q11-q13 deletions in Prader-Willi syndrome

被引：51

作者：

Carrozzo, R

Rossi, E

Christian, SL

Kittikamron, K

Livieri, C

Corrias, A

Pucci, L

Fois, A

Simi, P

Bosio, L

Beccaria, L

Zuffardi, O

Ledbetter, DH

机构：

[1] UNIV CHICAGO,CTR MED GENET,CHICAGO,IL 60637

[2] UNIV MILAN,OSPED SAN RAFFAELE,SERV GENET MED,I-20127 MILAN,ITALY

[3] UNIV MILAN,OSPED SAN RAFFAELE,LAB CITOGENET,I-20127 MILAN,ITALY

[4] UNIV MILAN,OSPED SAN RAFFAELE,CLIN PEDIAT 3,I-20127 MILAN,ITALY

[5] TIGEM,MILAN,ITALY

[6] UNIV PAVIA,PEDIAT CLIN,I-27100 PAVIA,ITALY

[7] OSPED INFANTILE REGINA MARGHERITA,DIV ENDOCRINOL PEDIAT,TURIN,ITALY

[8] UNIV SIENA,PEDIAT CLIN,I-53100 SIENA,ITALY

[9] UO AZIENDA OSPED PISANA,PISA,ITALY

来源：

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

关键词：

D O I：

10.1086/513907

中图分类号：

Q3 [遗传学];

学科分类号：

071007 ; 090102 ;

摘要：

引用

页码：228 / 231

页数：4

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