Rubinstein–Taybi syndrome in diverse populations - Tekendo
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a) Intraoral findings were a small mouth and malocclusion. (b) In
PDF) Rubinstein-Taybi syndrome: principal oral and dental disorders and literature update
Genes, Free Full-Text
PDF) FISH studies in 45 patients with Rubinstein-Taybi syndrome: Deletions associated with polysplenia, hypoplastic left heart and death in infancy
Facial clues to the photosensitive trichothiodystrophy phenotype in childhood
Rubinstein–Taybi syndrome in diverse populations - Tekendo‐Ngongang - 2020 - American Journal of Medical Genetics Part A - Wiley Online Library
Summary of deletion results. (a) Large deletions. A schematic
Wiley Special Collection on African Genomics: American Journal of Medical Genetics Part A
PDF) Rubinstein–Taybi syndrome 2 with cerebellar abnormality and neural tube defect
Expanding the genotypic and phenotypic spectrum in a diverse cohort of 104 individuals with Wiedemann‐Steiner syndrome - Sheppard - 2021 - American Journal of Medical Genetics Part A - Wiley Online Library
Expanding the genotypic and phenotypic spectrum in a diverse cohort of 104 individuals with Wiedemann‐Steiner syndrome - Sheppard - 2021 - American Journal of Medical Genetics Part A - Wiley Online Library
Main clinical signs of the thirty-one Italian RSTS patients.
Characteristics of RTS.
Identification of CREBBP mutation. A, Pedigree of family affected by
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