Born with Rubinstein-Taybi Syndrome (RTS), Braxton and Family are
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After an uneventful pregnancy, I arrived at the hospital ready to meet my son and introduce him […]
Rubinstein–Taybi syndrome European Journal of Human Genetics
Our - The Rubinstein-Taybi Syndrome Children's Foundation
Rubinstein–Taybi syndrome in diverse populations - Tekendo‐Ngongang - 2020 - American Journal of Medical Genetics Part A - Wiley Online Library
What is Rubinstein-Taybi Syndrome? - Goally Apps & Tablets for Kids
Severe persistent pulmonary hypertension in a neonate with Rubinstein–Taybi syndrome accompanied by triple X syndrome - Pediatrics & Neonatology
What is RTS? Rubinstein-Taybi Syndrome
A case with Rubinstein-Taybi syndrome: A novel frameshift mutation in the CREBBP gene.
To the People Who Think I'm 'Jumping on the Bandwagon' on Rare Disease Day
What is RTS? Rubinstein-Taybi Syndrome
Whole exome sequencing reveals de novo pathogenic variants in KAT6A as a cause of a neurodevelopmental disorder - Millan - 2016 - American Journal of Medical Genetics Part A - Wiley Online Library
De Novo Nonsense Mutations in KAT6A, a Lysine Acetyl-Transferase Gene, Cause a Syndrome Including Microcephaly and Global Developmental Delay - ScienceDirect
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