Rubinstein-Taybi syndrome - Atlas of Human Malformation Syndromes
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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 - Atlas of Human Malformation Syndromes in Diverse Populations
Rubinstein-Taybi Syndrome: A Complete Overview — DermNet
Atlas of Human Malformation Syndromes in Diverse Populations
Chromosome 16p13.3 Deletion Syndrome, Proximal disease: Malacards - Research Articles, Drugs, Genes, Clinical Trials
File:Rubinstein-Taybi Syndrome1.jpg - Wikipedia
Rubinstein–Taybi syndrome: New neuroradiological and neuropsychiatric insights from a multidisciplinary approach - Ajmone - 2018 - American Journal of Medical Genetics Part B: Neuropsychiatric Genetics - Wiley Online Library
Congenital Malformations and Syndromes: Early Diagnosis and Prognosis in Neonatal Medicine
PDF) Rubinstein-Taybi syndrome: Clinical features, genetic basis, diagnosis, and management
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