Nail dystrophy associated with a heterozygous mutation of the nude/SCID human FOXM1 (WHN) bone

被引：22

作者：

Auricchio, L ^{[1
]}

Adriani, M ^{[1
]}

Frank, J ^{[1
]}

Busiello, R ^{[1
]}

Christiano, A ^{[1
]}

Pignata, C ^{[1
]}

机构：

[1] Univ Naples Federico II, Dept Pediat, Immunol Unit, I-80131 Naples, Italy

来源：

ARCHIVES OF DERMATOLOGY | 2005年 / 141卷 / 05期

关键词：

D O I：

10.1001/archderm.141.5.647

中图分类号：

R75 [皮肤病学与性病学];

学科分类号：

100206 [皮肤病与性病学];

摘要：

[No abstract available]

引用

页码：647 / 648

页数：2

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[2]

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[3]

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[4]

Pignata C, 1996, AM J MED GENET, V65, P167, DOI 10.1002/(SICI)1096-8628(19961016)65:2<167::AID-AJMG17>3.0.CO

[5]

2-O

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