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
Heterogeneous genetic landscape of congenital neutropenia in
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
Phenotypic expansion of KMT2D‐related disorder: Beyond Kabuki
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
Three-Generation Family With Congenital Central Hypoventilation
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
TTC5 syndrome: Clinical and molecular spectrum of a severe and
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
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
A Novel CREBBP in-Frame Deletion Variant in a Chinese Girl with
de por adulto (o preço varia de acordo com o tamanho do grupo)