14q(22) deletion in a familial case of anophthalmia with polydactyly
Author:
Publisher
Wiley
Subject
Genetics (clinical)
Reference17 articles.
1. Deletion 14q (q22q23) associated with anophthalmia, absent pituitary, and other abnormalities.
2. Congenital eye malformations: Clinical-epidemiological analysis of 1,124,654 consecutive births in Spain
3. Compiling a national register of babies born with anophthalmia/microphthalmia in England 1988-94
4. Clinical anophthalmia: An epidemiological study in Northeast Italy based on 368,256 consecutive births
5. Geographical variation in anophthalmia and microphthalmia in England, 1988-94 Commentary: Clustering of anophthalmia and microphthalmia is not supported by the data
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2. Genetic Abnormalities With Anophthalmia, Microphthalmia, and Colobomas;Ophthalmic Genetic Diseases;2019
3. INVOLVEMENT OF MULTIPLE MOLECULAR PATHWAYS IN THE GENETICS OF OCULAR REFRACTION AND MYOPIA;Retina;2018-01
4. Interstitial deletion 14q22.3-q23.2: Genotype-phenotype correlation;American Journal of Medical Genetics Part A;2013-12-19
5. A CASE OF FAMILIAL BILATERAL ANOPHTHALMOS WITH SYNDACTYLY;Journal of Evolution of medical and Dental Sciences;2013-02-16
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