Novel mutation ofTBX3 in a Japanese family with Ulnar-Mammary syndrome: Implication for impaired sex development
Author:
Publisher
Wiley
Subject
Genetics (clinical)
Reference21 articles.
1. Clinical analysis of a large kindred with the Pallister ulnar-mammary syndrome
2. Mutations in human TBX3 alter limb, apocrine and genital development in ulnar-mammary syndrome
3. The Spectrum of Mutations in TBX3: Genotype/Phenotype Relationship in Ulnar-Mammary Syndrome
4. An ancient family of embryonically expressed mouse genes sharing a conserved protein motif with the T locus
5. Expression of the T-box family genes,Tbx1-Tbx5, during early mouse development
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