about
A novel 11p13 microdeletion encompassing PAX6 in a Chinese Han family with aniridia, ptosis and mental retardation.Improving molecular diagnosis of aniridia and WAGR syndrome using customized targeted array-based CGHA nonsense PAX6 mutation in a family with congenital aniridia.Congenital Aniridia: Clinic, Genetics, Therapeutics, and Prognosis.Parental Mosaicism in Causes Intra-Familial Variability: Implications for Genetic Counseling of Congenital Aniridia and Microphthalmia
P2860
description
article científic
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article scientifique
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articol științific
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articolo scientifico
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artigo científico
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artigo científico
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artigo científico
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artikel ilmiah
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artikull shkencor
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artículo científico
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name
Guidelines for genetic study of aniridia.
@en
type
label
Guidelines for genetic study of aniridia.
@en
prefLabel
Guidelines for genetic study of aniridia.
@en
P2093
P1476
Guidelines for genetic study of aniridia
@en
P2093
C Villaverde-Montero
F Blanco-Kelly
I Lorda-Sánchez
J M Millán
M J Trujillo-Tiebas
P304
P356
10.1016/J.OFTAL.2012.07.006
P50
P577
2012-09-25T00:00:00Z