La Sindrome di Marshall-Smith - EURORDIS
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
Sotos and Marshall Smith syndromes explained by gene mutation, Queensland scientists find - ABC News
Phoenix's Life With Marshall Smith Syndrome - YouTube
Distinct Effects of Allelic NFIX Mutations on Nonsense-Mediated mRNA Decay Engender Either a Sotos-like or a Marshall-Smith Syndrome - ScienceDirect
Three Dutch kids with the very rare Marshall-Smith Syndrom… | Flickr
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PDF) Marshall-Smith Syndrome: a distinct entity
Unusual features in a child with Marshall-Smith syndrome due to a novel NFIX variant: Evidence for an abnormal protein function - ScienceDirect
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MSS (Marshall Smith Syndrome) Research Foundation | The Hague
Mattéo - marshallsmith.org
![PDF] A Grain of Normality Weaning a Child With Marshall-Smith Syndrome From the Feeding Tube: A Case Report | Semantic Scholar](https://d3i71xaburhd42.cloudfront.net/87edc93420fda779179d29519b92f323153382d1/3-Figure1-1.png "PDF] A Grain of Normality Weaning a Child With Marshall-Smith Syndrome From the Feeding Tube: A Case Report | Semantic Scholar")
PDF] A Grain of Normality Weaning a Child With Marshall-Smith Syndrome From the Feeding Tube: A Case Report | Semantic Scholar
MSS... - MSS (Marshall Smith Syndrome) Research Foundation
Home - marshallsmith.org
Home - marshallsmith.org
Mobilisation autour de Colleen, 7 ans, atteinte d'une maladie rare - La Voix du Nord
Wow!... - MSS (Marshall Smith Syndrome) Research Foundation | Facebook
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: Natural history and evidence of an osteochondrodysplasia with connective tissue abnormalities - Adam - 2005 - American Journal of Medical Genetics Part A - Wiley Online Library
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Casa - marshallsmith.org
Novel mutations of NFIX gene causing Marshall-Smith syndrome or Sotos-like syndrome: one gene, two phenotypes | Pediatric Research
Marshall-Smith syndrome: Novel pathogenic variant and previously unreported associations with precocious puberty and aortic root dilatation - ScienceDirect
![PDF] Marshall-Smith Syndrome in a Chinese Boy | Semantic Scholar](https://d3i71xaburhd42.cloudfront.net/933a4f46ff01f8ce6710042decf65ce0022f889b/2-Figure1-1.png "PDF] Marshall-Smith Syndrome in a Chinese Boy | Semantic Scholar")