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

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

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

Phoenix's Life With Marshall Smith Syndrome - YouTube
Phoenix's Life With Marshall Smith Syndrome - YouTube

Marshall-Smith Syndrome: Reaching for the STARS - EURORDIS
Marshall-Smith Syndrome: Reaching for the STARS - EURORDIS

Mosaicism in Stickler syndrome. | Semantic Scholar
Mosaicism in Stickler syndrome. | Semantic Scholar

Marshall syndrome
Marshall syndrome

Clinical features of type 2 Stickler syndrome | Journal of Medical Genetics
Clinical features of type 2 Stickler syndrome | Journal of Medical Genetics

Home - marshallsmith.org
Home - marshallsmith.org

Indian Pediatrics - Editorial
Indian Pediatrics - Editorial

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

Spontaneous Rupture of the Lens Capsule in a Case of Marshall Syndrome | Journal of Pediatric Ophthalmology & Strabismus
Spontaneous Rupture of the Lens Capsule in a Case of Marshall Syndrome | Journal of Pediatric Ophthalmology & Strabismus

Stickler Syndrome and Homoeopathy – Kavitha K Homeo
Stickler Syndrome and Homoeopathy – Kavitha K Homeo

Maxillomandibular distraction osteogenesis for Marshall–Smith syndrome - ScienceDirect
Maxillomandibular distraction osteogenesis for Marshall–Smith syndrome - ScienceDirect

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

Syndrome de Marshall : symptômes, diagnostic et traitement : Femme Actuelle Le MAG
Syndrome de Marshall : symptômes, diagnostic et traitement : Femme Actuelle Le MAG

Marshall syndrome - wikidoc
Marshall syndrome - wikidoc

Phenotype and natural history in Marshall–Smith syndrome - Shaw - 2010 - American Journal of Medical Genetics Part A - Wiley Online Library
Phenotype and natural history in Marshall–Smith syndrome - Shaw - 2010 - American Journal of Medical Genetics Part A - Wiley Online Library

Atlas Entry - Marshall Syndrome
Atlas Entry - Marshall Syndrome

Stickler Marshall Syndrome: Adelaide boy with rare genetic condition living mainstream life with specialist intervention | The Advertiser
Stickler Marshall Syndrome: Adelaide boy with rare genetic condition living mainstream life with specialist intervention | The Advertiser

File:Marshall syndrome.jpg - Wikimedia Commons
File:Marshall syndrome.jpg - Wikimedia Commons

Sotos and Marshall Smith syndromes explained by gene mutation, Queensland scientists find - ABC News
Sotos and Marshall Smith syndromes explained by gene mutation, Queensland scientists find - ABC News

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

▷ Is Marshall syndrome - PFAPA hereditary?
▷ Is Marshall syndrome - PFAPA hereditary?

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
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

Novel mutations of NFIX gene causing Marshall-Smith syndrome or Sotos-like syndrome: one gene, two phenotypes | Pediatric Research
Novel mutations of NFIX gene causing Marshall-Smith syndrome or Sotos-like syndrome: one gene, two phenotypes | Pediatric Research

Stickler syndrome: MedlinePlus Genetics
Stickler syndrome: MedlinePlus Genetics

Genes | Free Full-Text | Hearing Loss in Stickler Syndrome: An Update
Genes | Free Full-Text | Hearing Loss in Stickler Syndrome: An Update

Home - marshallsmith.org
Home - marshallsmith.org

Stickler Syndrome: Symptoms & Outlook
Stickler Syndrome: Symptoms & Outlook

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