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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
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

Indian Pediatrics - Editorial
Indian Pediatrics - Editorial

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

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

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

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

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

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

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

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

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

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

Marshall syndrome - wikidoc
Marshall syndrome - wikidoc

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

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

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

Home - marshallsmith.org
Home - marshallsmith.org

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

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

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

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

Home - marshallsmith.org
Home - marshallsmith.org

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

Atlas Entry - Marshall Syndrome
Atlas Entry - Marshall Syndrome

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