Facial dysmorphism, skeletal anomalies, congenital glucoma
Por um escritor misterioso
Last updated 25 janeiro 2025
Congenital Malformations of the Eye and Orbit
Full article: Retinal detachment in a child with Frank-ter Haar syndrome
Axenfeld–Rieger syndrome: orthopedic and orthodontic management in a pediatric patient: a case report, Head & Face Medicine
Clinical phenotype of family BDCS1. The facial features of BDCS1-17 at
Facial dysmorphism, skeletal anomalies, congenital glucoma, dysplastic nails: Mild Rubinstein-Taybi Syndrome - ScienceDirect
PDF) Cornelia de Lange Syndrome with Congenital Glaucoma
Anterior segment developmental disorders - ScienceDirect
Facial dysmorphism, skeletal anomalies, congenital glucoma, dysplastic nails: Mild Rubinstein-Taybi Syndrome - ScienceDirect
TASP1 mutation in a female with craniofacial anomalies, anterior segment dysgenesis, congenital immunodeficiency and macrocytic anemia - Balkin - 2019 - Molecular Genetics & Genomic Medicine - Wiley Online Library
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