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Splicing Mutations of 54-bp Exons in the COL11A1 Gene Cause Marshall Syndrome, but Other Mutations Cause Overlapping Marshall/Stickler Phenotypes - ScienceDirect
Splicing Mutations of 54-bp Exons in the COL11A1 Gene Cause Marshall Syndrome, but Other Mutations Cause Overlapping Marshall/Stickler Phenotypes - ScienceDirect

PDF] Marshall-Smith Syndrome in a Chinese Boy | Semantic Scholar
PDF] Marshall-Smith Syndrome in a Chinese Boy | Semantic Scholar

Marshall Stickler Syndrome, My Cleft Palate & Me - Write Like No One's Watching
Marshall Stickler Syndrome, My Cleft Palate & Me - Write Like No One's Watching

Marshall Syndrome
Marshall Syndrome

Family circle - marshallsmith.org
Family circle - marshallsmith.org

Acquired Cutis Laxa Type II (Marshall Syndrome) in an 18‐Month‐Old Child: A Case Report - Haider - 2010 - Pediatric Dermatology - Wiley Online Library
Acquired Cutis Laxa Type II (Marshall Syndrome) in an 18‐Month‐Old Child: A Case Report - Haider - 2010 - Pediatric Dermatology - Wiley Online Library

Marshall-Smith syndrome: Novel pathogenic variant and previously unreported associations with precocious puberty and aortic root dilatation - ScienceDirect
Marshall-Smith syndrome: Novel pathogenic variant and previously unreported associations with precocious puberty and aortic root dilatation - ScienceDirect

Marshall syndrome: definition and causes, Learn More
Marshall syndrome: definition and causes, Learn More

Marshall-Smith Syndrome OMIM# 602535 - FDNA
Marshall-Smith Syndrome OMIM# 602535 - FDNA

LSUHSC School of Medicine
LSUHSC School of Medicine

Stickler Syndrome and Homoeopathy | Kavitha K Homeo
Stickler Syndrome and Homoeopathy | Kavitha K Homeo

A rare case of stickler marshall syndrome Gurnani B, Kaur K - TNOA J Ophthalmic Sci Res
A rare case of stickler marshall syndrome Gurnani B, Kaur K - TNOA J Ophthalmic Sci Res

Marshall syndrome causes, symptoms, diagnosis, treatment & prognosis
Marshall syndrome causes, symptoms, diagnosis, treatment & prognosis

The Marshall-Smith syndrome: a review of the laryngeal complications | Semantic Scholar
The Marshall-Smith syndrome: a review of the laryngeal complications | Semantic Scholar

Marshall syndrome - Flipbook by DLaws0620 | FlipHTML5
Marshall syndrome - Flipbook by DLaws0620 | FlipHTML5

Maxillomandibular distraction osteogenesis for Marshall–Smith syndrome - Journal of Plastic, Reconstructive & Aesthetic Surgery
Maxillomandibular distraction osteogenesis for Marshall–Smith syndrome - Journal of Plastic, Reconstructive & Aesthetic Surgery

Marshall Syndrome Associated with a Splicing Defect at the COL11A1 Locus - ScienceDirect
Marshall Syndrome Associated with a Splicing Defect at the COL11A1 Locus - ScienceDirect

Marshall-Smith syndrome: case report of a newborn male and review of the literature. - Abstract - Europe PMC
Marshall-Smith syndrome: case report of a newborn male and review of the literature. - Abstract - Europe PMC

PDF] Marshall's syndrome* | Semantic Scholar
PDF] Marshall's syndrome* | Semantic Scholar

Marshall syndrome causes, symptoms, diagnosis, treatment & prognosis
Marshall syndrome causes, symptoms, diagnosis, treatment & prognosis

Novel and recurrent COL11A1 and COL2A1 mutations in the Marshall–Stickler syndrome spectrum | Human Genome Variation
Novel and recurrent COL11A1 and COL2A1 mutations in the Marshall–Stickler syndrome spectrum | Human Genome Variation

STICKLER SYNDROME Corrine Fillman, M.S., C.G.C. - ppt video online download
STICKLER SYNDROME Corrine Fillman, M.S., C.G.C. - ppt video online download

Home - marshallsmith.org
Home - marshallsmith.org

Sweet's syndrome leading to acquired cutis laxa in a child (Marshall's syndrome): A rare case report Bangaru H, Surendran K, Nanjundaswamy B L, Vijaya B - Indian J Paediatr Dermatol
Sweet's syndrome leading to acquired cutis laxa in a child (Marshall's syndrome): A rare case report Bangaru H, Surendran K, Nanjundaswamy B L, Vijaya B - Indian J Paediatr Dermatol

Facial phenotype: (A) MS71 I:1; (B) MS71 II:2; (C) MS1 II:6; (D) MS1... | Download Scientific Diagram
Facial phenotype: (A) MS71 I:1; (B) MS71 II:2; (C) MS1 II:6; (D) MS1... | Download Scientific Diagram

Unusual features in a child with Marshall-Smith syndrome due to a novel NFIX variant: Evidence for an abnormal protein function - ScienceDirect
Unusual features in a child with Marshall-Smith syndrome due to a novel NFIX variant: Evidence for an abnormal protein function - ScienceDirect