Rubinstein-Taybi syndrome - Atlas of Human Malformation Syndromes
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Rubinstein-Taybi syndrome - Atlas of Human Malformation Syndromes in Diverse Populations
PDF] Rubinstein-Taybi Syndrome Associated with Pituitary Macroadenoma: A Case Report
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
Canal Dehiscense
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
A case with Rubinstein-Taybi syndrome: A novel frameshift mutation in the CREBBP gene.
Dandy walker variant an association with Rubinstein Taybi syndrome
Congenital Malformations and Syndromes: Early Diagnosis and Prognosis in Neonatal Medicine
Facial features and limb anomalies of all the patients: a Facial
Rubinstein-Taybi syndrome - Atlas of Human Malformation Syndromes in Diverse Populations
Glaucoma and Findings Simulating Glaucoma in the Rubinstein-Taybi Syndrome
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
Mosaic CREBBP mutation causes overlapping clinical features of Rubinstein– Taybi and Filippi syndromes
PDF) Rubinstein-Taybi syndrome with deletions of FISH probe RT1 at 16p13.3: Two UK patients
PDF) New dysmorphic features in Rubinstein-Taybi syndrome
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