The novel and recurrent variants in exon 31 of CREBBP in Japanese patients with Menke–Hennekam syndrome - Nishi - 2022 - American Journal of Medical Genetics Part A - Wiley Online Library
Por um escritor misterioso
Descrição
Heterogeneous genetic landscape of congenital neutropenia in
The missing link between genetic association and regulatory
Phenotypic expansion of KMT2D‐related disorder: Beyond Kabuki
Three-Generation Family With Congenital Central Hypoventilation
The novel and recurrent variants in exon 31 of CREBBP in Japanese
PDF) Menke–Hennekam Syndrome: A Literature Review and a New Case
TTC5 syndrome: Clinical and molecular spectrum of a severe and
Genotype–phenotype specificity in Menke–Hennekam syndrome caused
PDF) Menke–Hennekam Syndrome: A Literature Review and a New Case
A Novel CREBBP in-Frame Deletion Variant in a Chinese Girl with
de
por adulto (o preço varia de acordo com o tamanho do grupo)