Rubinstein–Taybi syndrome associated with Chiari type I malformation caused by a large 16p13.3 microdeletion: A contiguous gene syndrome? - Wójcik - 2010 - American Journal of Medical Genetics Part A - Wiley Online Library
Por um escritor misterioso
Descrição
Clinical, genetic and imaging findings identify new causes for
Rubinstein–Taybi syndrome in diverse populations - Tekendo
Frontiers Genetic Diagnosis of Rubinstein–Taybi Syndrome With
Molecular studies in 10 cases of Rubinstein-Taybi syndrome
Rubinstein–Taybi syndrome: New neuroradiological and
Rubinstein–Taybi syndrome associated with Chiari type I
Mosaic CREBBP mutation causes overlapping clinical features of
Frontiers Genetic Diagnosis of Rubinstein–Taybi Syndrome With
Frontiers Case Report: Low-Level Maternal Mosaicism of a Novel
Chromosome 16p13.3 Deletion Syndrome, Proximal disease: Malacards
Rubinstein–Taybi syndrome: New neuroradiological and
Rubinstein–Taybi syndrome associated with Chiari type I
PDF) Rubinstein-Taybi syndrome: Clinical features, genetic basis
Clinical, genetic and imaging findings identify new causes for
de
por adulto (o preço varia de acordo com o tamanho do grupo)
