Frontiers Case report: A preterm infant with rubinstein-taybi
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Frontiers in Pediatrics
Rubinstein-Taybi Syndrome: A Case Report
Frontiers in Pediatrics Genetics of Common and Rare Diseases
Low bone mineral density on DXA and slipped capital femoral epiphysis as rare presentation in a child with Rubinstein-Taybi syndrome
Abstracts - 2023 - Congenital Anomalies - Wiley Online Library
a,b: Patient A at 3 weeks; c,d: Patient B at 6 weeks, note the opening
Frontiers in Pediatrics
Low bone mineral density on DXA and slipped capital femoral epiphysis as rare presentation in a child with Rubinstein-Taybi syndrome
A Novel CREBBP in-Frame Deletion Variant in a Chinese Girl with Atypical Rubinstein–Taybi Syndrome Phenotypes
Rubinstein-Taybi Syndrome: A Pediatric Case Report
Frontiers Case report: A preterm infant with rubinstein-taybi syndrome and Marmorata telangiectatica harboring a frameshift mutation in the CREBBP gene
Frontiers in Pediatrics Genetics of Common and Rare Diseases
JPM, Free Full-Text
Lucja Bieleninik - Norce
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