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
Last updated 27 dezembro 2024
The missing link between genetic association and regulatory
Multiple endocrine neoplasia type 2 (MEN2) and RET specific
A Novel CREBBP in-Frame Deletion Variant in a Chinese Girl with
De novo heterozygous Hb G-Waimanalo (α64(E13)Asp>Asn, CTG>CCG
Genes, Free Full-Text
Okamoto syndrome has features overlapping with Au–Kline syndrome
Community‐based recruitment and exome sequencing indicates high
Genotype–phenotype specificity in Menke–Hennekam syndrome caused
De novo ANKRD11 and KDM1A gene mutations in a male with features
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