Meet Phoenix: A Children's Wisconsin Champion
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Marshall-Smith syndrome: case report of a newborn male and review of the literature. - Abstract - Europe PMC
Novel and recurrent COL11A1 and COL2A1 mutations in the Marshall–Stickler syndrome spectrum | Human Genome Variation
Marshall syndrome causes, symptoms, diagnosis, treatment & prognosis
Sweet's syndrome leading to acquired cutis laxa in a child (Marshall's syndrome): A rare case report | Semantic Scholar
Alternative splicing modifies the effect of mutations in COL11A1 and results in recessive type 2 Stickler syndrome with profound hearing loss | Journal of Medical Genetics
Family's Bittersweet Journey Spares One Son From Rare Disease, But Not the Other - ABC News
Speaking About Top Diseases in the Marshall Islands
Dynamics of health and disease: Carter L. Marshall: 9780390598936: Amazon.com: Books
Accueil - marshallsmith.org
Accueil - marshallsmith.org
Novel mutations of NFIX gene causing Marshall-Smith syndrome or Sotos-like syndrome: one gene, two phenotypes | Pediatric Research
Syndrome de Marshall : symptômes, diagnostic et traitement : Femme Actuelle Le MAG
Marshall syndrome | PPT
Unusual features in a child with Marshall-Smith syndrome due to a novel NFIX variant: Evidence for an abnormal protein function - ScienceDirect
Marshall syndrome causes, symptoms, diagnosis, treatment & prognosis
Family's Bittersweet Journey Spares One Son From Rare Disease, But Not the Other - ABC News
Marshall Syndrome disease: Malacards - Research Articles, Drugs, Genes, Clinical Trials
Marshall Syndrome | Hereditary Ocular Diseases
Sotos and Marshall Smith syndromes explained by gene mutation, Queensland scientists find - ABC News
![PDF] Marshall's syndrome* | Semantic Scholar](https://d3i71xaburhd42.cloudfront.net/8692715a2d8f922bfa0e453fcf08fdb91bfa259c/2-Figure2-1.png "PDF] Marshall's syndrome* | Semantic Scholar")