rubinstein taybi

  • A novel CREBBP mutation and its phenotype in a case of Rubinstein–Taybi syndrome, BMC Medical Genomics

A novel CREBBP mutation and its phenotype in a case of Rubinstein–Taybi syndrome, BMC Medical Genomics
  • Social Skills

Social Skills
  • Molecular studies in 10 cases of Rubinstein-Taybi syndrome, including a mild variant showing a missense mutation in codon 1175 of CREBBP

Molecular studies in 10 cases of Rubinstein-Taybi syndrome, including a mild variant showing a missense mutation in codon 1175 of CREBBP
  • What Is Rubinstein-Taybi Syndrome? - StoryMD

What Is Rubinstein-Taybi Syndrome? - StoryMD
  • Rubinstein-Taybi syndrome - Atlas of Human Malformation Syndromes

Rubinstein-Taybi syndrome - Atlas of Human Malformation Syndromes
  • Molecular studies in 10 cases of Rubinstein-Taybi syndrome

Molecular studies in 10 cases of Rubinstein-Taybi syndrome
  • 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
  • A case of bilateral elbow dislocation in a patient with Rubinstein

A case of bilateral elbow dislocation in a patient with Rubinstein
  • Mosaic CREBBP mutation causes overlapping clinical features of Rubinstein– Taybi and Filippi syndromes

Mosaic CREBBP mutation causes overlapping clinical features of Rubinstein– Taybi and Filippi syndromes
  • Rubinstein - Taybi syndrome: phenotypic characteristics

Rubinstein - Taybi syndrome: phenotypic characteristics
  • Rubinstein-Taybi syndrome - Atlas of Human Malformation Syndromes in Diverse Populations

Rubinstein-Taybi syndrome - Atlas of Human Malformation Syndromes in Diverse Populations
  • Congenital glaucoma as a presenting feature of Rubinstein-Taybi

Congenital glaucoma as a presenting feature of Rubinstein-Taybi
  • A novel CREBBP mutation and its phenotype in a case of Rubinstein

A novel CREBBP mutation and its phenotype in a case of Rubinstein
  • Rubinstein-Taybi Syndrome OMIM# 180849 - FDNA™

Rubinstein-Taybi Syndrome OMIM# 180849 - FDNA™
  • Rubinstein–Taybi syndrome in diverse populations - Tekendo

Rubinstein–Taybi syndrome in diverse populations - Tekendo
  • Long-term results following osteotomy of the thumb delta phalanx

Long-term results following osteotomy of the thumb delta phalanx
  • Facial dysmorphism, skeletal anomalies, congenital glucoma, dysplastic nails: Mild Rubinstein-Taybi Syndrome - ScienceDirect

Facial dysmorphism, skeletal anomalies, congenital glucoma, dysplastic nails: Mild Rubinstein-Taybi Syndrome - ScienceDirect
  • Rubinstein–Taybi syndrome: clinical and molecular overview, Expert Reviews in Molecular Medicine

Rubinstein–Taybi syndrome: clinical and molecular overview, Expert Reviews in Molecular Medicine
  • Rubinstein-Taybi syndrome: MedlinePlus Genetics

Rubinstein-Taybi syndrome: MedlinePlus Genetics
  • Minha história: Christiane, Isabela e a síndrome de Rubinstein

Minha história: Christiane, Isabela e a síndrome de Rubinstein

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