## Abstract Rapid advances in new basic knowledge have led to a greater understanding of the genetic, embryologic, molecular biologic, and functional mechanisms underlying the ectodermal dysplasias. Scientists, researchers, and clinicians from diverse fields desire a classification that meets the n
โฆ LIBER โฆ
Ectodermal dysplasias: An overview and update of clinical and molecular-functional mechanisms
โ Scribed by Manuela Priolo
- Publisher
- John Wiley and Sons
- Year
- 2009
- Tongue
- English
- Weight
- 200 KB
- Volume
- 149A
- Category
- Article
- ISSN
- 1552-4825
No coin nor oath required. For personal study only.
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## Abstract We report on a patient with an interstitial deletion of the long arm of chromosome 2 at 2q31.2q33.2. She had prenatal and postnatal growth retardation, microcephaly, facial dysmorphism, cleft palate, camptodactyly, bilateral talipes equinovarus, severe intellectual disability, and ectod