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Marshall-Smith Syndrome: Reaching for the STARS - eurordis.org
Marshall-Smith Syndrome: Reaching for the STARS - eurordis.org

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

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

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

Home - marshallsmith.org
Home - marshallsmith.org

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

and Congenital Anomalies | Ento Key
and Congenital Anomalies | Ento Key

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

Indian Pediatrics - Editorial
Indian Pediatrics - Editorial

Genetics of Neonatal Airway Disorders | SpringerLink
Genetics of Neonatal Airway Disorders | SpringerLink

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

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

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

Fronto-orbital advancement in a patient with Marshall-Smith syndrome: a case report and review of the literature | SpringerLink
Fronto-orbital advancement in a patient with Marshall-Smith syndrome: a case report and review of the literature | SpringerLink

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

Phoenix Hatch, diagnosed with Marshall Smith Syndrome 2 months after birth. Life expectancy is 18 months, Phoenix is now … | Life expectancy, Hair styles, Awareness
Phoenix Hatch, diagnosed with Marshall Smith Syndrome 2 months after birth. Life expectancy is 18 months, Phoenix is now … | Life expectancy, Hair styles, Awareness

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

Sweet's syndrome leading to acquired cutis laxa in a child (Marshall's syndrome): A rare case report | Semantic Scholar
Sweet's syndrome leading to acquired cutis laxa in a child (Marshall's syndrome): A rare case report | Semantic Scholar

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

Home - marshallsmith.org
Home - marshallsmith.org

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

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
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

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

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