A de novo TBX3 mutation presenting as dorsalization of the little fingers: A forme fruste phenotype of ulnar-mammary syndrome
Author:
Funder
King Salman Center for Disability Research
Publisher
Elsevier BV
Subject
Genetics (clinical),Genetics,General Medicine
Reference13 articles.
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3. Dorsal dimelia: report of two cases with an emphasis on the variation of phenotypic expression and a search for candidate causative genes;Al-Qattan;J Hand Surg Eur,2010
4. GLI3-related polydactyly: a review;Al-Qattan;Clin. Genet.,2017
5. The spectrum of mutations in TBX3: genotype/Phenotype relationship in ulnar-mammary syndrome;Bamshad;Am. J. Hum. Genet.,1999
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3. Literature review, report, and analysis of genotype and clinical phenotype of a rare case of ulnar-mammary syndrome;Frontiers in Pediatrics;2023-03-03
4. TBX3 and EFNA4 Variant in a Family with Ulnar-Mammary Syndrome and Sagittal Craniosynostosis;Genes;2022-09-14
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