p63 gene analysis in Mexican patients with syndromic and non-syndromic ectrodactyly-Reference-Cited by-同舟云学术

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p63 gene analysis in Mexican patients with syndromic and non-syndromic ectrodactyly

Published:2004-01 Issue:1 Volume:22 Page:1-5
ISSN:0736-0266
Container-title:Journal of Orthopaedic Research
language:en
Short-container-title:J. Orthop. Res.

Author:

Berdón-Zapata V.,Granillo-Álvarez M.,Valdés-Flores M.,García-Ortiz J. E.,Kofman-Alfaro S.,Zenteno J. C.

Publisher

Wiley

Subject

Orthopedics and Sports Medicine

Reference22 articles.

1. TP63 gene mutation in ADULT syndrome

2. Analysis of the p63 gene in classical EEC syndrome, related syndromes, and non-syndromic orofacial clefts

3. The p63 gene in EEC and other syndromes

4. Heterozygous Germline Mutations in the p53 Homolog p63 Are the Cause of EEC Syndrome

5. An epidemiological study of isolated split hand/foot in Hungary, 1975-1984.

Cited by 18 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. TP63 mutation mapping information in TP63 mutation-associated syndromes;Advances in Oral and Maxillofacial Surgery;2022-01

2. Nonsyndromic Split-Hand/Foot Malformation: Recent Classification;Molecular Syndromology;2019

3. Genetic analysis of a congenital split‑hand/split‑foot malformation 4 pedigree;Molecular Medicine Reports;2018-03-29

4. A double dealing tale of p63: an oncogene or a tumor suppressor;Cellular and Molecular Life Sciences;2017-10-03

5. Molecular Genetic Characterization of a Chinese Family with Severe Split Hand/Foot Malformation;Genetic Testing and Molecular Biomarkers;2017-06

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