Molecular studies in 10 cases of Rubinstein-Taybi syndrome

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Molecular studies in 10 cases of Rubinstein-Taybi syndrome
Clinical photos of the patients. (a) Case 1: Dysmorphic facial features
Molecular studies in 10 cases of Rubinstein-Taybi syndrome
Oral and Dental Manifestations in Rubinstein-Taybi Syndrome: Report of a Rare Case
Molecular studies in 10 cases of Rubinstein-Taybi syndrome
PDF) CREBBP and EP300 mutational spectrum and clinical presentations in a cohort of Swedish patients with Rubinstein–Taybi syndrome
Molecular studies in 10 cases of Rubinstein-Taybi syndrome
Rubinstein-Taybi syndrome in a Saudi boy with distinct features and variants in both the CREBBP and EP300 genes: a case report, BMC Medical Genetics
Molecular studies in 10 cases of Rubinstein-Taybi syndrome
Epigenetic mechanisms of Rubinstein-Taybi syndrome. - Abstract - Europe PMC
Molecular studies in 10 cases of Rubinstein-Taybi syndrome
Clinical characteristics of present cohort of patients with
Molecular studies in 10 cases of Rubinstein-Taybi syndrome
CREBBP mutations in individuals without Rubinstein–Taybi syndrome phenotype - Menke - 2016 - American Journal of Medical Genetics Part A - Wiley Online Library
Molecular studies in 10 cases of Rubinstein-Taybi syndrome
Rubinstein Syndrome - an overview
Molecular studies in 10 cases of Rubinstein-Taybi syndrome
Ocular features in Rubinstein-Taybi syndrome: investigation of 24 patients and review of the literature
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