Telomeric 22q13 deletions resulting from rings, simple deletions, and translocations: cytogenetic, molecular, and clinical analyses of 32 new observations

被引:98
作者
Luciani, JJ
de Mas, P
Depetris, D
Mignon-Ravix, C
Bottani, A
Prieur, M
Jonveaux, P
Philippe, A
Bourrouillou, G
de Martinville, B
Delobel, B
Vallee, L
Croquette, MF
Mattei, MG
机构
[1] Fac Med Marseille, INSERM, U491, F-13385 Marseille, France
[2] CHU Purpan, Serv Genet, Toulouse, France
[3] Fac Med, Div Med Genet, Geneva, Switzerland
[4] Hop Necker Enfants Malad, Cytogenet Serv, Paris, France
[5] Hop Necker Enfants Malad, Unite Genet Clin, Paris, France
[6] CHU Brabois, Genet Lab, Vandoeuvre Les Nancy, France
[7] Hop Jeanne de Flandre, Med Genet Lab, Lille, France
[8] Hop St Antoine, Lab Cytogenet, Lille, France
[9] CHRU Lille, Serv Neurol Infantile, Lille, France
[10] Alliance 22, Frelinghien, France
关键词
D O I
10.1136/jmg.40.9.690
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
引用
收藏
页码:690 / 696
页数:7
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