Published in
Elsevier, European Journal of Medical Genetics, 10(63), p. 104010, 2020
DOI: 10.1016/j.ejmg.2020.104010
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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
Journal article published in 2020 by
Renee Carroll,
Marie Shaw,
Maria Arvio,
Alison Gardner,
Raman Kumar,
Bree Hodgson,
Sarah Heron 
,
Fiona McKenzie,
Irma Järvelä,
Jozef Gecz
,
Fiona McKenzie,
Irma Järvelä,
Jozef Gecz
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