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Results 1 - 7 of 7 for Sillence syndrome
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  1. COL1A1 gene 
    ... N, Zschocke J, Malfait F. The Ehlers-Danlos syndromes, rare types. Am J Med ... Abuzahra H, Couper R, Mundlos S, Sillence D, Ala Kokko L, Seidman JG, Cole WG, ...
    https://medlineplus.gov/genetics/gene/col1a1 - Genetics
  2. COL1A2 gene 
    ... autosomal recessive cardiac valvular form of Ehlers-Danlos syndrome results from ... DO. Osteogenesis imperfecta: clinical diagnosis, nomenclature and severity ...
    https://medlineplus.gov/genetics/gene/col1a2 - Genetics
  3. FBN1 gene 
    ... Mortier G, Odent S, Polak M, Rohrbach M, Sillence D, Stolte-Dijkstra I, Superti-Furga A, Rimoin ...
    https://medlineplus.gov/genetics/gene/fbn1 - Genetics
  4. COL2A1 gene 
    ... T, Le Merrer M, Leroy JG, Coucke PJ, Sillence D, Mortier GR. Czech dysplasia metatarsal type: another ... MP. Variation in the vitreous phenotype of Stickler syndrome can be caused by different amino acid substitutions ...
    https://medlineplus.gov/genetics/gene/col2a1 - Genetics
  5. MESP2 gene 
    ... on PubMed Whittock NV, Sparrow DB, Wouters MA, Sillence D, Ellard S, Dunwoodie SL, Turnpenny PD. Mutated ...
    https://medlineplus.gov/genetics/gene/mesp2 - Genetics
  6. CHST3 gene 
    ... Unger S, Lausch E, Rossi A, Megarbane A, Sillence D, Alcausin M, Aytes A, Mendoza-Londono R, ...
    https://medlineplus.gov/genetics/gene/chst3 - Genetics
  7. PYCR1 gene 
    ... Sommer A, Savarirayan R, Janecke AR, Steichen E, Sillence D, Hausser I, Budde B, Nurnberg G, Nurnberg ...
    https://medlineplus.gov/genetics/gene/pycr1 - Genetics