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
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Last updated 12 abril 2025


Genotype–phenotype specificity in Menke–Hennekam syndrome caused

Genotype–phenotype specificity in Menke–Hennekam syndrome caused

Further delineation of an entity caused by CREBBP and EP300

The novel and recurrent variants in exon 31 of CREBBP in Japanese

KRIT1 mutations in three Japanese pedigrees with hereditary

Novel exon-skipping variant disrupting the basic domain of HCFC1

The novel and recurrent variants in exon 31 of CREBBP in Japanese

Novel NTRK1 mutations in Chinese patients with congenital

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