Refinement and delineation of the breakpoint regions of a chromosome 1;22 translocation in a patient with Costello syndrome

被引：9

作者：

Maróti, Z

Kutsche, K

Sutajova, M

Gal, A

Nothwang, HG

Czeizel, AE

Tímár, L

Sólyom, E

机构：

[1] Univ Klinikum Hamburg Eppendorf, Inst Humangenet, D-22529 Hamburg, Germany

[2] Max Planck Inst Mol Genet, Berlin, Germany

[3] OKK Csaladtervezesi Kozpont, Budapest, Hungary

[4] Borsod Cty Teaching Hosp, Miskolc, Hungary

来源：

AMERICAN JOURNAL OF MEDICAL GENETICS | 2002年 / 109卷 / 03期

关键词：

D O I：

10.1002/ajmg.10314

中图分类号：

Q3 [遗传学];

学科分类号：

071007 ; 090102 ;

摘要：

引用

页码：234 / 237

页数：4

共 7 条

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[7] Costello syndrome with acoustic neuroma and cataract. Is the Costello locus linked to neurofibromatosis type 2 on 22q? [J].

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