Rubinstein-Taybi syndrome - Atlas of Human Malformation Syndromes
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Diagnostic analysis of the Rubinstein-Taybi syndrome: five cosmids should be used for microdeletion detection and low number of protein truncating mutations
PDF) Rubinstein-Taybi syndrome in diverse populations
The natural history of adults with Rubinstein-Taybi syndrome: a families-reported experience
Possible case of Rubinstein‐Taybi syndrome in a prehistoric skeleton from west‐central Illinois - Wilbur - 2000 - American Journal of Medical Genetics - Wiley Online Library
High frequency of copy number imbalances in Rubinstein–Taybi patients negative to CREBBP mutational analysis
Glaucoma and Findings Simulating Glaucoma in the Rubinstein-Taybi Syndrome
Rubinstein–Taybi syndrome European Journal of Human Genetics
Rubinstein‐Taybi Syndrome in a Fetus: Contribution of 2‐ and 3‐Dimensional Ultrasonography - Cardalliac - 2018 - Journal of Ultrasound in Medicine - Wiley Online Library
Congenital Malformations and Syndromes: Early Diagnosis and Prognosis in Neonatal Medicine
KMT2C/D COMPASS complex-associated diseases [KCDCOM-ADs]: an emerging class of congenital regulopathies, Clinical Epigenetics
Rubinstein-Taybi syndrome with scoliosis treated with single-stage posterior spinal fusion: illustrative case in: Journal of Neurosurgery: Case Lessons Volume 1 Issue 11 (2021) Journals
Rubinstein-Taybi syndrome - Atlas of Human Malformation Syndromes in Diverse Populations
File:Rubinstein-Taybi Syndrome1.jpg - Wikipedia
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
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