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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PDF) Menke–Hennekam Syndrome: A Literature Review and a New Case
The missing link between genetic association and regulatory
Frontiers Case Report: Low-Level Maternal Mosaicism of a Novel
KRIT1 mutations in three Japanese pedigrees with hereditary
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Multiple endocrine neoplasia type 2 (MEN2) and RET specific
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The novel and recurrent variants in exon 31 of CREBBP in Japanese
The novel and recurrent variants in exon 31 of CREBBP in Japanese
A Novel CREBBP in-Frame Deletion Variant in a Chinese Girl with
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