Marshall syndrome: Further evidence of a distinct phenotypic entity and report of new findings
Indian Pediatrics - Editorial
Fronto-orbital advancement in a patient with Marshall-Smith syndrome: a case report and review of the literature | SpringerLink
Alex Richter-Boix on Twitter: "El síndrome de Marshall es un trastorno genético que se caracteriza por un aumento en el grosor del cráneo y una estructura facial con alteraciones. https://t.co/WRx1j4c4E2" / Twitter
![PDF] Marshall's syndrome* | Semantic Scholar](https://d3i71xaburhd42.cloudfront.net/8692715a2d8f922bfa0e453fcf08fdb91bfa259c/2-Figure2-1.png "PDF] Marshall's syndrome* | Semantic Scholar")
PDF] Marshall's syndrome* | Semantic Scholar
Marshall syndrome - wikidoc
Stickler Syndrome | SpringerLink
Home - marshallsmith.org
A rare case of stickler marshall syndrome
LSUHSC School of Medicine
Phenotype and natural history in Marshall–Smith syndrome - Shaw - 2010 - American Journal of Medical Genetics Part A - Wiley Online Library
Clinical features of type 2 Stickler syndrome | Journal of Medical Genetics
Marshall syndrome causes, symptoms, diagnosis, treatment & prognosis
File:Marshall syndrome.jpg - Wikimedia Commons
Stickler Syndrome: Symptoms & Outlook
Novel mutations of NFIX gene causing Marshall-Smith syndrome or Sotos-like syndrome: one gene, two phenotypes | Pediatric Research
Genes | Free Full-Text | Hearing Loss in Stickler Syndrome: An Update
PDF) Marshall-Smith Syndrome: a distinct entity
Atlas Entry - Marshall Syndrome
Wow!... - MSS (Marshall Smith Syndrome) Research Foundation | Facebook
STICKLER SYNDROME Corrine Fillman, M.S., C.G.C. - ppt video online download
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
Maxillomandibular distraction osteogenesis for Marshall–Smith syndrome - 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")
PDF] Marshall-Smith Syndrome in a Chinese Boy | Semantic Scholar
Acquired Cutis Laxa Type II (Marshall Syndrome) in an 18‐Month‐Old Child: A Case Report - Haider - 2010 - Pediatric Dermatology - Wiley Online Library
