Swyer syndrome and 46,XY partial gonadal dysgenesis associated with 9p deletions in the absence of monosomy-9p syndrome

被引：56

作者：

Veitia, RA

Nunes, M

Quintana-Murci, L

Rappaport, R

Thibaud, E

Jaubert, E

Fellous, M

McElreavey, K

Goncalves, J

Silva, M

Rodrigues, JC

Caspurro, M

Boieiro, F

Marques, R

Lavinha, J

机构：

[1] Inst Pasteur, INSERM, U276, F-75015 Paris, France

[2] Hop Necker Enfants Malad, Serv Endocrinol, Paris, France

[3] Hop Necker Enfants Malad, Serv Cent Antomie Pathol, Paris, France

[4] Inst Nacl Saude Dr Ricardo Jorge, Dept Human Genet, Lisbon, Portugal

[5] Hosp Criancas Maria Pia, Serv Cirurg Pediat, Oporto, Portugal

[6] Hosp Santo Antonio, Serv Anat Patol, Porto, Portugal

来源：

AMERICAN JOURNAL OF HUMAN GENETICS | 1998年 / 63卷 / 03期

关键词：

D O I：

10.1086/302023

中图分类号：

Q3 [遗传学];

学科分类号：

071007 ; 090102 ;

摘要：

引用

页码：901 / 905

页数：5

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