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 96 for CG 11
  1. Collagen VI-related dystrophy 
    ... AR, Mohassel P, Donkervoort S, Bolduc V, Bonnemann CG. Collagen VI-Related Dystrophies. 2004 Jun 25 [updated 2021 Mar 11]. In: Adam MP, Feldman J, Mirzaa GM, Pagon ...
    https://medlineplus.gov/.../condition/collagen-vi-related-myopathy - Genetics
  2. Autosomal recessive primary microcephaly 
    ... Free article on PubMed Central Thornton GK, Woods CG. Primary microcephaly: do all roads lead to Rome? Trends Genet. 2009 Nov;25(11):501-10. doi: 10.1016/j.tig.2009. ...
    https://medlineplus.gov/.../autosomal-recessive-primary-microcephaly - Genetics
  3. SELENON gene 
    ... Kress W, Bonnemann CG, Breitbach-Faller N, Korenke CG, Schreiber G, Stoetter M, Ferreiro A, von der Hagen M. The phenotype and long-term follow-up in 11 patients with juvenile selenoprotein N1-related myopathy. Eur ...
    https://medlineplus.gov/genetics/gene/selenon - Genetics
  4. 15q13.3 microdeletion 
    ... J, Bachman K, Troxell R, Clark G, Minard CG, Stankiewicz P, Beaudet A, Schaaf CP. The complex behavioral phenotype of 15q13.3 microdeletion syndrome. Genet Med. 2016 Nov;18(11):1111-1118. doi: 10.1038/gim.2016.9. ...
    https://medlineplus.gov/genetics/condition/15q133-microdeletion - Genetics
  5. ASPM gene 
    ... RK, Sharif SM, Bennett C, Glover DM, Woods CG, Morrison EE, Bond J. Human ASPM participates in spindle organisation, spindle orientation and cytokinesis. BMC Cell Biol. 2010 Nov 2;11:85. doi: 10.1186/1471-2121-11-85. ...
    https://medlineplus.gov/genetics/gene/aspm - Genetics
  6. ALG12 gene 
    ... Apr 30. Citation on PubMed Grubenmann CE, Frank CG, Kjaergaard S, Berger EG, Aebi M, Hennet T. ALG12 mannosyltransferase defect in congenital disorder of glycosylation type lg. Hum Mol Genet. 2002 Sep 15;11(19):2331-9. doi: 10.1093/hmg/11. ...
    https://medlineplus.gov/genetics/gene/alg12 - Genetics
  7. ALG12-congenital disorder of glycosylation 
    ... Apr 30. Citation on PubMed Grubenmann CE, Frank CG, Kjaergaard S, Berger EG, Aebi M, Hennet T. ALG12 mannosyltransferase defect in congenital disorder of glycosylation type lg. Hum Mol Genet. 2002 Sep 15;11(19):2331-9. doi: 10.1093/hmg/11. ...
    https://medlineplus.gov/...lg12-congenital-disorder-of-glycosylation - Genetics
  8. LMNA-related congenital muscular dystrophy 
    ... j.nmd.2011.08.009. Epub 2012 Jan 11. Citation on PubMed Heller F, Dabaj I, Mah JK, Bergounioux J, Essid A, Bonnemann CG, Rutkowski A, Bonne G, Quijano-Roy S, Wahbi ...
    https://medlineplus.gov/...mna-related-congenital-muscular-dystrophy - Genetics
  9. FGFR3 gene 
    ... No abstract available. Citation on PubMed L'Hote CG, Knowles MA. Cell responses to FGFR3 signalling: growth, differentiation and apoptosis. Exp Cell Res. 2005 Apr 1;304(2):417-31. doi: 10.1016/j.yexcr.2004.11.012. Epub 2004 Dec 16. Citation on PubMed ...
    https://medlineplus.gov/genetics/gene/fgfr3 - Genetics
  10. ATG16L1 gene 
    ... B, Folsch UR, Lengauer T, Platzer M, Mathew CG, Krawczak M, Schreiber S. A genome-wide association scan of nonsynonymous SNPs identifies a susceptibility variant for Crohn disease in ATG16L1. Nat Genet. 2007 Feb;39(2):207-11. doi: 10.1038/ng1954. Epub 2006 Dec 31. ...
    https://medlineplus.gov/genetics/gene/atg16l1 - Genetics
previous · 1 · 2 · 3 · 4 · 5 · 6 · 7 · 8 · 9 · 10 · next