Coloboma Associated With Rubinstein-Taybi Syndrome
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Frontiers Genetic Diagnosis of Rubinstein–Taybi Syndrome With Multiplex Ligation-Dependent Probe Amplification (MLPA) and Whole-Exome Sequencing (WES): Case Series With a Novel CREBBP Variant
Rubinstein-Taybi Syndrome
Rubinstein-Taybi Syndrome
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
KoreaMed Synapse
Genetics of syndromic ocular coloboma: CHARGE and COACH syndromes - ScienceDirect
Genes, Free Full-Text
Rubinstein–Taybi syndrome in diverse populations - Tekendo‐Ngongang - 2020 - American Journal of Medical Genetics Part A - Wiley Online Library
Journal of Pediatric Ophthalmology 1974: Vol 11 Index : Free Download, Borrow, and Streaming : Internet Archive
Coloboma - EyeWiki
A novel CREBBP mutation and its phenotype in a case of Rubinstein–Taybi syndrome, BMC Medical Genomics