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
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Phenotype and natural history in Marshall–Smith syndrome - Shaw - 2010 - American Journal of Medical Genetics Part A - Wiley Online Library
Maxillomandibular distraction osteogenesis for Marshall–Smith syndrome - ScienceDirect
Atlas Entry - Marshall Syndrome
Marshall Syndrome Associated with a Splicing Defect at the COL11A1 Locus - ScienceDirect
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Genetics of Neonatal Airway Disorders | SpringerLink
Unusual features in a child with Marshall-Smith syndrome due to a novel NFIX variant: Evidence for an abnormal protein function - ScienceDirect
and Congenital Anomalies | Ento Key
Clinical features of type 2 Stickler syndrome | Journal of Medical Genetics
Marshall syndrome
Marshall syndrome - Flipbook by DLaws0620 | FlipHTML5
▷ Is Marshall syndrome - PFAPA hereditary?
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
![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
A rare case of stickler marshall syndrome
Sweet's syndrome leading to acquired cutis laxa in a child (Marshall's syndrome): A rare case report | Semantic Scholar
STICKLER SYNDROME Corrine Fillman, M.S., C.G.C. - ppt video online download
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Stickler Marshall Syndrome: Adelaide boy with rare genetic condition living mainstream life with specialist intervention | The Advertiser
Novel and recurrent COL11A1 and COL2A1 mutations in the Marshall–Stickler syndrome spectrum | Human Genome Variation
Splicing Mutations of 54-bp Exons in the COL11A1 Gene Cause Marshall Syndrome, but Other Mutations Cause Overlapping Marshall/Stickler Phenotypes - ScienceDirect
Marshall syndrome - wikidoc
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A report on 10 new patients with heterozygous mutations in the COL11A1 gene and a review of genotype–phenotype correlations in type XI collagenopathies - Majava - 2007 - American Journal of Medical
Acquired Cutis Laxa Type II (Marshall Syndrome) in an 18‐Month‐Old Child: A Case Report - Haider - 2010 - Pediatric Dermatology - Wiley Online Library
