The Rubinstein-Taybi syndrome: a report of two cases.
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Novel heterozygous variants in the EP300 gene cause Rubinstein–Taybi syndrome 2: Reports from two Chinese children,Molecular Genetics & Genomic Medicine - X-MOL
PDF) Rubinstein-Taybi syndrome medical guidelines
PDF) Rubinstein-Taybi syndrome medical guidelines
Rubinstein-Taybi syndrome: A report of two siblings with unreported cutaneous stigmata - Indian Journal of Dermatology, Venereology and Leprology
Rubinstein-Taybi Syndrome – New Indian Journal of Pediatrics
Molecular studies in 10 cases of Rubinstein-Taybi syndrome, including a mild variant showing a missense mutation in codon 1175 of CREBBP
Dysmorphic and skeletal features of Rubinstein‐Taybi syndrome patients.
Rubinstein-Taybi Syndrome
PDF) Rubinstein-Taybi syndrome medical guidelines
Rubinstein–Taybi syndrome in diverse populations - Tekendo‐Ngongang - 2020 - American Journal of Medical Genetics Part A - Wiley Online Library
Ultrasound 2-D and 3-D diagnosis of Rubinstein–Taybi syndrome in a 21-week-old fetus
Inheritance and variable expression in Rubinstein–Taybi syndrome - Bartsch - 2010 - American Journal of Medical Genetics Part A - Wiley Online Library
PDF] Rubinstein-Taybi Syndrome: A Case Report
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