Syndromic and non-syndromic GLI3 phenotypes
Author:
Publisher
Wiley
Subject
Genetics(clinical),Genetics
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1399-0004.2005.0485a.x/fullpdf
Reference4 articles.
1. Molecular analysis of non-syndromic preaxial polydactyly: preaxial polydactyly type-IV and preaxial polydactyly type-I;Fujioka;Clin Genet,2005
2. Molecular and clinical analyses of Greig cephalopolysyndactyly and Pallister-Hall syndromes: robust phenotype prediction from the type and position of GLI3 mutations;Johnston;Am J Hum Genet,2005
3. Morphogenesis: Re: Clinical, natural history, and imaging information on patients included in reports;Aylsworth;Am J Med Genet,2003
4. A clinician's plea;Hall;Nat Genet,2003
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1. Molecular Bases of Human Malformation Syndromes Involving the SHH Pathway: GLIA/R Balance and Cardinal Phenotypes;International Journal of Molecular Sciences;2021-12-02
2. NovelGLI3variant causes Greig cephalopolysyndactyly syndrome in three generations of a Lithuanian family;Molecular Genetics & Genomic Medicine;2019-07-20
3. Preaxial polydactyly of the foot;Acta Orthopaedica;2017-09-26
4. The disruption of a novel limb cis-regulatory element of SHH is associated with autosomal dominant preaxial polydactyly-hypertrichosis;European Journal of Human Genetics;2015-03-18
5. New insights into genotype–phenotype correlation for GLI3 mutations;European Journal of Human Genetics;2014-04-16
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