Frontiers Case report: A preterm infant with rubinstein-taybi
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Heart Failure in Pediatric Patients With Congenital Heart Disease
novel frameshift mutation - List of Frontiers' open access articles
PDF] Chromosome 16p13.3 Contiguous Gene Deletion Syndrome including the SLX4, DNASE1, TRAP1, and CREBBP Genes Presenting as a Relatively Mild Rubinstein–Taybi Syndrome Phenotype: A Case Report of a Saudi Boy
Frontiers in Pediatrics
novel frameshift mutation - List of Frontiers' open access articles
Role of Environmental Epigenetics in Perinatal and Neonatal Development
Physical features in RSTS patients. (A) Evolution of the phenotype from
Children With Disabilities, PDF, Preterm Birth
Frontiers Risk Factors for Adverse Neurodevelopment in Transient or Persistent Congenital Hyperinsulinism
Frontiers Risk Factors for Adverse Neurodevelopment in Transient or Persistent Congenital Hyperinsulinism
Frontiers in Pediatrics
Disease mechanisms of monogenic congenital anomalies of the kidney and urinary tract - Connaughton - 2022 - American Journal of Medical Genetics Part C: Seminars in Medical Genetics - Wiley Online Library
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
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