GLI3-related polydactyly: a review-Reference-Cited by-同舟云学术

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GLI3-related polydactyly: a review

Published:2017-02-22 Issue:5 Volume:92 Page:457-466
ISSN:0009-9163
Container-title:Clinical Genetics
language:en
Short-container-title:Clin Genet

Author:

Al-Qattan M.M.¹,Shamseldin H.E.²,Salih M.A.³,Alkuraya F.S.²⁴

Affiliation:

1. Department of Surgery, College of Medicine; King Saud University; Riyadh Saudi Arabia

2. Department of Genetics; King Faisal Specialist Hospital and Research Center; Jeddah Saudi Arabia

3. Department of Pediatrics, College of Medicine; King Saud University; Riyadh Saudi Arabia

4. Department of Anatomy and Cell Biology, College of Medicine; Alfaisal University; Riyadh Saudi Arabia

Funder

College of Medicine Research Center

Deanship of Scientific Research

King Saud University, Riyadh, Saudi Arabia

Publisher

Wiley

Subject

Genetics(clinical),Genetics

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1111/cge.12952/fullpdf

Reference74 articles.

1. Strike three for GLI3;Biesecker;Nat Genet,1997

2. The phenotypic spectrum of GLI3 morphopathies includes autosomal dominant preaxial polydactyly type IV and postaxial polydactyly type A/B; No phenotype prediction from the position of GLI3 mutations;Radhakrishna;Am J Hum Genet,1999

3. Molecular analysis expands the spectrum of phenotypes associated with GLI3 mutations;Johnston;Hum Mutat,2010

4. Polydactyly: phenotypes, genetics and classification;Malik;Clin Genet,2014

5. Pallister-Hall syndrome has gone the way of modern medical genetics;Hall;Am J Med Genet C Semin Med Genet,2014

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1. A novel GLI3 frameshift mutation in a Chinese pedigree with polydactyly: A case report;Heliyon;2024-04

2. Morphological changes and hub genes screening in rats with anorectal malformations during hindgut development;Journal of Pediatric Surgery Open;2024-04

3. Paternal age and risk for selected birth defects in a large South American sample;Birth Defects Research;2023-09-20

4. Advances in hypothalamic hamartoma research over the past 30 years (1992–2021): a bibliometric analysis;Frontiers in Neurology;2023-06-06

5. FOXI3 pathogenic variants cause one form of craniofacial microsomia;Nature Communications;2023-04-11

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