Marshall Stickler Syndrome, My Cleft Palate & Me - Write Like No One's Watching
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
Marshall Syndrome
The Marshall-Smith syndrome: a review of the laryngeal complications | Semantic Scholar
Phenotype and natural history in Marshall–Smith syndrome - Shaw - 2010 - American Journal of Medical Genetics Part A - Wiley Online Library
Phoenix's Life With Marshall Smith Syndrome - YouTube
Phoenix Hatch, diagnosed with Marshall Smith Syndrome 2 months after birth. Life expectancy is 18 months, Phoenix is now 4 years… | Life expectancy, Awareness, Body
Novel mutations of NFIX gene causing Marshall-Smith syndrome or Sotos-like syndrome: one gene, two phenotypes | Pediatric Research
Marshall Stickler Syndrome, My Cleft Palate & Me - Write Like No One's Watching
Marshall syndrome
Marshall syndrome: definition and causes, Learn More
Splicing Mutations of 54-bp Exons in the COL11A1 Gene Cause Marshall Syndrome, but Other Mutations Cause Overlapping Marshall/Stickler Phenotypes - ScienceDirect
LSUHSC School of Medicine
A rare case of stickler marshall syndrome Gurnani B, Kaur K - TNOA J Ophthalmic Sci Res
Marshall-Smith syndrome: case report of a newborn male and review of the literature. - Abstract - Europe PMC
Unusual features in a child with Marshall-Smith syndrome due to a novel NFIX variant: Evidence for an abnormal protein function - ScienceDirect
Stickler Syndrome and Homoeopathy | Kavitha K Homeo