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Phoenix Hatch, diagnosed with Marshall Smith Syndrome 2 months after birth. Life expectancy is 18 months, Phoenix is now … | Life expectancy, Hair styles, Awareness
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Phenotype and natural history in Marshall–Smith syndrome - Shaw - 2010 - American Journal of Medical Genetics Part A - Wiley Online Library
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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
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Novel and recurrent COL11A1 and COL2A1 mutations in the Marshall–Stickler syndrome spectrum | Human Genome Variation
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Novel mutations of NFIX gene causing Marshall-Smith syndrome or Sotos-like syndrome: one gene, two phenotypes | Pediatric Research
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Acquired Cutis Laxa Type II (Marshall Syndrome) in an 18‐Month‐Old Child: A Case Report - Haider - 2010 - Pediatric Dermatology - Wiley Online Library
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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
Stickler Marshall Syndrome: Adelaide boy with rare genetic condition living mainstream life with specialist intervention | The Advertiser
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