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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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
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
A Novel CREBBP in-Frame Deletion Variant in a Chinese Girl with
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
The novel and recurrent variants in exon 31 of CREBBP in Japanese
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
PDF) Menke–Hennekam Syndrome: A Literature Review and a New Case
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
Genotype–phenotype specificity in Menke–Hennekam syndrome caused
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
The novel and recurrent variants in exon 31 of CREBBP in Japanese
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
Frontiers Novel Gross Deletion Mutations in NTRK1 Gene
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
KRIT1 mutations in three Japanese pedigrees with hereditary
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
A Novel CREBBP in-Frame Deletion Variant in a Chinese Girl with
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
Facial morphology of the presently described patient with the
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
The novel and recurrent variants in exon 31 of CREBBP in Japanese
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
PDF) Menke–Hennekam Syndrome: A Literature Review and a New Case

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