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 10 novembro 2024
Novel exon-skipping variant disrupting the basic domain of HCFC1
Genotype–phenotype specificity in Menke–Hennekam syndrome caused
The novel and recurrent variants in exon 31 of CREBBP in Japanese
A novel SYNJ1 homozygous variant causing developmental and
The novel and recurrent variants in exon 31 of CREBBP in Japanese
Diagnosis of Menke‐Hennekam syndrome by prenatal whole exome
The novel and recurrent variants in exon 31 of CREBBP in Japanese
TTC5 syndrome: Clinical and molecular spectrum of a severe and
Genomic profiling of 553 uncharacterized neurodevelopment patients
The novel and recurrent variants in exon 31 of CREBBP in Japanese
The missing link between genetic association and regulatory
Genotype–phenotype specificity in Menke–Hennekam syndrome caused
Novel CLTC variants cause new brain and kidney phenotypes
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