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Two novel intragenic variants in the FMR1 gene in patients with suspect clinical diagnosis of Fragile X syndrome and no CGG repeat expansion |
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Titel: |
Two novel intragenic variants in the FMR1 gene in patients with suspect clinical diagnosis of Fragile X syndrome and no CGG repeat expansion |
Auteur: |
Carroll, Renee Shaw, Marie Arvio, Maria Gardner, Alison Kumar, Raman Hodgson, Bree Heron, Sarah McKenzie, Fiona Järvelä, Irma Gecz, Jozef |
Verschenen in: |
European journal of medical genetics |
Paginering: |
Jaargang 63 () nr. 10 pagina's p. |
Jaar: |
2020 |
Inhoud: |
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Uitgever: |
Elsevier Masson SAS |
Bronbestand: |
Elektronische Wetenschappelijke Tijdschriften |
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