Rubinstein-Taybi Syndrome
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Rubinstein-Taybi syndrome: MedlinePlus Genetics
Rubinstein-Taybi syndrome, Radiology Reference Article
Facial dysmorphism, skeletal anomalies, congenital glucoma, dysplastic nails: Mild Rubinstein-Taybi Syndrome - ScienceDirect
Exon deletions of the EP300 and CREBBP genes in two children with Rubinstein –Taybi syndrome detected by aCGH
IJMS, Free Full-Text
Rubinstein-Taybi Syndrome
Rubinstein-Taybi Syndrome Info Bank • RTS Support Group
DBMCI MDS : Formerly MDS Experts - RUBINSTEIN TAYBI SYNDROME An autosomal dominant disease associated with deletions of the short arm of ch 16. Clinical Features: - Mental retardation - Broad thumbs
Rubinstein–Taybi Syndrome in a Filipino Infant with a Novel CREBBP Gene Pathogenic Variant
Congenital glaucoma as a presenting feature of Rubinstein-Taybi syndrome in an infant with a novel pathogenic variant in the CREBBP gene
Rubinstein-Taybi syndrome-showing distinctive clinical features like
Ocular features in Rubinstein-Taybi syndrome: investigation of 24 patients and review of the literature
Pediatric on Squares on X: Rubinstein Taybi Syndrome #Pediatric #Genetics # syndrome / X
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