Phenotype and natural history in Marshall–Smith syndrome - Shaw - 2010 - American Journal of Medical Genetics Part A - Wiley Online Library
Malan syndrome: Sotos-like overgrowth with de novo NFIX sequence variants and deletions in six new patients and a review of the literature | European Journal of Human Genetics
Syndrome de Marshall-Smith - EURORDIS
Marshall–Smith syndrome: Natural history and evidence of an osteochondrodysplasia with connective tissue abnormalities - Adam - 2005 - American Journal of Medical Genetics Part A - Wiley Online Library
What is MSS? - marshallsmith.org
Sotos and Marshall Smith syndromes explained by gene mutation, Queensland scientists find - ABC News
Marshall–Smith syndrome: Natural history and evidence of an osteochondrodysplasia with connective tissue abnormalities - Adam - 2005 - American Journal of Medical Genetics Part A - Wiley Online Library
Marshall-Smith Syndrome OMIM# 602535 - FDNA™
Zeldzame Ziekten Fonds Marshall-Smith Syndroom - Zeldzame Ziekten Fonds
Marshall-Smith syndrome: Novel pathogenic variant and previously unreported associations with precocious puberty and aortic root dilatation - ScienceDirect
Phoenix's Life With Marshall Smith Syndrome - YouTube
Home - marshallsmith.org
Distinct Effects of Allelic NFIX Mutations on Nonsense-Mediated mRNA Decay Engender Either a Sotos-like or a Marshall-Smith Syndrome - ScienceDirect
PDF) Marshall-Smith syndrome: a distinct entity | Ashutosh Halder - Academia.edu
Unusual features in a child with Marshall-Smith syndrome due to a novel NFIX variant: Evidence for an abnormal protein function - ScienceDirect
Mobilisation autour de Colleen, 7 ans, atteinte d'une maladie rare - La Voix du Nord
Marshall–Smith syndrome: Natural history and evidence of an osteochondrodysplasia with connective tissue abnormalities - Adam - 2005 - American Journal of Medical Genetics Part A - Wiley Online Library
A standard of care for the ultra-rare Marshall-Smith syndrome - developmental process and lessons learned | Semantic Scholar
Novel mutations of NFIX gene causing Marshall-Smith syndrome or Sotos-like syndrome: one gene, two phenotypes | Pediatric Research
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