Clinical features of a family with X-linked amelogenesis imperfecta mapping to a new locus (AIH3) on the long arm of the X chromosome
- 31 August 1993
- journal article
- Published by Elsevier in Oral Surgery, Oral Medicine, Oral Pathology
- Vol. 76 (2) , 187-191
- https://doi.org/10.1016/0030-4220(93)90203-g
Abstract
No abstract availableKeywords
This publication has 5 references indexed in Scilit:
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- Genetic heterogeneity in X-linked amelogenesis imperfectaGenomics, 1992
- X-linked amelogenesis imperfecta: Presentation of two kindreds and a review of the literatureOral Surgery, Oral Medicine, Oral Pathology, 1992
- A deletion in the amelogenin gene (AMG) causes X-linked amelogenesis imperfecta (AIH1)Genomics, 1991
- Partial expression of sex-linked recessive amelogenesis imperfecta in females compatible with the Lyon hypothesisOral Surgery, Oral Medicine, Oral Pathology, 1967