Rubinstein-Taybi Syndrome 1
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A novel CREBBP mutation and its phenotype in a case of Rubinstein–Taybi syndrome, BMC Medical Genomics
Patent Ductus Arteriousus Device Closure in an Infant with Rubinstein–Taybi Syndrome, Iranian Journal of Pediatrics
Rubinstein-Taybi Syndrome: Child Characteristics and Parental Perception Noorwijkerhout Ina van Berckelaer-Onnes & Josette Wulffaert. - ppt download
Rubinstein-Taybi Syndrome: A Complete Overview — DermNet
Rubinstein-Taybi Syndrome 1
Psychiatric Profile in Rubinstein-Taybi Syndrome
Fetal phenotype of Rubinstein‐Taybi syndrome caused by CREBBP mutations - Van‐Gils - 2019 - Clinical Genetics - Wiley Online Library
Born with Rubinstein-Taybi Syndrome (RTS), Braxton and Family are Full of Hope - Global Genes
Analysis of mutations within the intron20 splice donor site of CREBBP in patients with and without classical RSTS
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: A case report
Dermatologic Manifestations of Rubinstein-Taybi Syndrome Clinical Presentation: History, Physical Examination, Complications
4 Newborn with Rubinstein-Taybi syndrome showing microcephaly, frontal
Low bone mineral density on DXA and slipped capital femoral epiphysis as rare presentation in a child with Rubinstein-Taybi syndrome
Rubinstein-Taybi Syndrome
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