Skip navigation

Official websites use .gov
A .gov website belongs to an official government organization in the United States.

Secure .gov websites use HTTPS
A lock ( ) or https:// means you’ve safely connected to the .gov website. Share sensitive information only on official, secure websites.

Results 1 - 10 of 13 for Sillence syndrome
Did you mean silence syndrome?
  1. Kleefstra syndrome 
    ... Heaps L, Peters G, Sholler G, Tzioumi D, Sillence DO, Mowat D. Three patients ... chromosome 9q subtelomere deletion syndrome. Am J Med Genet C Semin Med Genet. ...
    https://medlineplus.gov/genetics/condition/kleefstra-syndrome - Genetics
  2. 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
  3. 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
  4. 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
  5. Frontometaphyseal dysplasia 
    ... Kim CA, Krakow D, Morava E, Neuhann T, Sillence D, Superti-Furga A, Veenstra-Knol HE, Wieczorek ...
    https://medlineplus.gov/.../condition/frontometaphyseal-dysplasia - Genetics
  6. CHST3-related skeletal dysplasia 
    ... Unger S, Lausch E, Rossi A, Megarbane A, Sillence D, Alcausin M, Aytes A, Mendoza-Londono R, ...
    https://medlineplus.gov/.../chst3-related-skeletal-dysplasia - Genetics
  7. Spondylocostal dysostosis 
    ... on PubMed Whittock NV, Sparrow DB, Wouters MA, Sillence D, Ellard S, Dunwoodie SL, Turnpenny PD. Mutated ...
    https://medlineplus.gov/genetics/condition/spondylocostal-dysostosis - Genetics
  8. Caffey disease 
    ... Bastepe M, Abuzahra H, Couper R, Mundlos S, Sillence D, Ala Kokko L, Seidman JG, Cole WG, ...
    https://medlineplus.gov/genetics/condition/caffey-disease - Genetics
  9. 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
  10. 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
previous · 1 · 2 · next