4 Newborn with Rubinstein-Taybi syndrome showing microcephaly
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Genetic heterogeneity in Rubinstein–Taybi syndrome: delineation of the phenotype of the first patients carrying mutations in EP300
Genetic heterogeneity in Rubinstein–Taybi syndrome: delineation of the phenotype of the first patients carrying mutations in EP300
Rubinstein–Taybi syndrome in diverse populations - Tekendo‐Ngongang - 2020 - American Journal of Medical Genetics Part A - Wiley Online Library
Congenital Malformations and Syndromes: Early Diagnosis and Prognosis in Neonatal Medicine
File:Rubinstein-Taybi Syndrome1.jpg - Wikipedia
Rubinstein-Taybi Syndrome: A Complete Overview — DermNet
Rubinstein‐Taybi Syndrome in a Fetus: Contribution of 2‐ and 3‐Dimensional Ultrasonography - Cardalliac - 2018 - Journal of Ultrasound in Medicine - Wiley Online Library
JaypeeDigital
PDF) Patent ductus arteriousus device closure in an infant with rubinstein-taybi syndrome
Two patients with EP300 mutations and facial dysmorphism different from the classic Rubinstein–Taybi syndrome - Bartsch - 2010 - American Journal of Medical Genetics Part A - Wiley Online Library
Congenital Hypothyroidism Associated with Rubinstein-Taybi Syndrome
Rubinstein–Taybi Syndrome in a Filipino Infant with a Novel CREBBP Gene Pathogenic Variant
Rubinstein-Taybi 2 associated to novel EP300 mutations: deepening the clinical and genetic spectrum, BMC Medical Genetics
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