4 Newborn with Rubinstein-Taybi syndrome showing microcephaly
Por um escritor misterioso
Descrição
Rubinstein–Taybi syndrome in diverse populations - Tekendo‐Ngongang - 2020 - American Journal of Medical Genetics Part A - Wiley Online Library
JCM, Free Full-Text
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
CREBBP mutations in individuals without Rubinstein–Taybi syndrome phenotype - Menke - 2016 - American Journal of Medical Genetics Part A - Wiley Online Library
Seckel Syndrome: Most Up-to-Date Encyclopedia, News & Reviews
Congenital Hypothyroidism Associated with Rubinstein-Taybi Syndrome
MICROCEPHALY jo.pptx
Microcephaly
Case report: a Chinese girl like atypical Rubinstein–Taybi syndrome caused by a novel heterozygous mutation of the EP300 gene, BMC Medical Genomics
Congenital Malformations and Syndromes: Early Diagnosis and Prognosis in Neonatal Medicine
A Case of Rubinstein-Taybi Syndrome with Tetralogy of Fallot
Rubinstein–Taybi Syndrome in a Filipino Infant with a Novel CREBBP Gene Pathogenic Variant
4 Newborn with Rubinstein-Taybi syndrome showing microcephaly, frontal
Dermatologic Manifestations of Rubinstein-Taybi Syndrome Clinical Presentation: History, Physical Examination, Complications
Facial dysmorphism, skeletal anomalies, congenital glucoma, dysplastic nails: Mild Rubinstein-Taybi Syndrome - ScienceDirect
de
por adulto (o preço varia de acordo com o tamanho do grupo)
