Frontiers Case report: A preterm infant with rubinstein-taybi
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Frontiers Risk Factors for Adverse Neurodevelopment in Transient or Persistent Congenital Hyperinsulinism
A) sequence analysis of the genomic DNA of our rubinstein-taybi
Frontiers in Pediatrics
Lucja Bieleninik - Norce
of skull anomalies in Pfeiffer syndrome
Frontiers Case Report: Treatment of Extremely Preterm Infants With Birthweight Below 300 g: Case Series
Frontiers Case report: A preterm infant with rubinstein-taybi syndrome and Marmorata telangiectatica harboring a frameshift mutation in the CREBBP gene
Rubinstein–Taybi Syndrome in a Filipino Infant with a Novel CREBBP Gene Pathogenic Variant
PDF) Van Lohuizen Syndrome, a Late-Diagnosed Case in an 18 Years-Old Female
Frontiers Syndromic forms of congenital hyperinsulinism
Frontiers Impact of Comorbid Prematurity and Congenital Anomalies: A Review
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por adulto (o preço varia de acordo com o tamanho do grupo)
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