High frequencies of ICF syndrome-like pericentromeric heterochromatin decondensation and breakage in chromosome 1 in a chorionic villus sample

被引：7

作者：

Ehrlich, M

Tsien, F

Herrera, D

Blackman, V

Roggenbuck, J

Tuck-Muller, CM

机构：

[1] Tulane Univ, Sch Med, Human Genet Program, Hayward Genet Ctr, New Orleans, LA 70112 USA

[2] Tulane Univ, Sch Med, Dept Biochem, New Orleans, LA 70112 USA

[3] Alton Ochsner Med Fdn & Ochsner Clin, Dept Pediat, New Orleans, LA 70121 USA

[4] Alton Ochsner Med Fdn & Ochsner Clin, Dept Obstet & Gynecol, New Orleans, LA 70121 USA

[5] Univ S Alabama, Dept Med Genet, Mobile, AL 36688 USA

来源：

JOURNAL OF MEDICAL GENETICS | 2001年 / 38卷 / 12期

关键词：

D O I：

10.1136/jmg.38.12.882

中图分类号：

Q3 [遗传学];

学科分类号：

071007 ; 090102 ;

摘要：

引用

页码：882 / 884

页数：3

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