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Results 1 - 10 of 42 for Citation ID
  1. SLC46A1 gene 
    ... doi: 10.1016/j.cmet.2006.12.004. Citation on PubMed Goldman ID. Hereditary Folate Malabsorption. 2008 Jun 17 [updated 2024 ... doi: 10.1301/nr.2007.dec.554-557. Citation on PubMed Zhao R, Goldman ID. The molecular identity and characterization of a Proton- ...
    https://medlineplus.gov/genetics/gene/slc46a1 - Genetics
  2. SGO1 gene 
    ... tig.2012.03.003. Epub 2012 Apr 27. Citation on PubMed Krantz ID. Cohesin embraces new phenotypes. Nat Genet. 2014 Nov;46(11):1157-8. doi: 10.1038/ng.3123. Citation on PubMed or Free article on PubMed Central ...
    https://medlineplus.gov/genetics/gene/sgo1 - Genetics
  3. JAG1 gene 
    ... 1004(2001)17:13.0.CO;2-T. Citation on PubMed Spinner NB, Loomes KM, Krantz ID, Gilbert MA. Alagille Syndrome. 2000 May 19 [updated 2024 Jan 4]. In: Adam MP, Feldman J, Mirzaa GM, Pagon RA, Wallace SE, Bean LJH, Gripp KW, Amemiya A, ... Citation on PubMed
    https://medlineplus.gov/genetics/gene/jag1 - Genetics
  4. BEST1 gene 
    ... 1136/jmg.2008.059881. Epub 2008 Jul 8. Citation on PubMed Burgess R, Millar ID, Leroy BP, Urquhart JE, Fearon IM, De Baere ... doi: 10.1016/j.ajhg.2007.08.004. Citation on PubMed or Free article on PubMed Central Davidson AE, Millar ID, Urquhart JE, Burgess-Mullan R, Shweikh Y, Parry ...
    https://medlineplus.gov/genetics/gene/best1 - Genetics
  5. RPS6KA3 gene 
    ... doi: 10.1016/j.modgep.2003.06.001. Citation on PubMed Hanauer A, Young ID. Coffin-Lowry syndrome: clinical and molecular features. J Med Genet. 2002 Oct;39(10):705-13. doi: 10.1136/jmg.39.10.705. Citation on PubMed or Free article on PubMed Central ...
    https://medlineplus.gov/genetics/gene/rps6ka3 - Genetics
  6. NIPBL gene 
    ... doi: 10.1086/424698. Epub 2004 Aug 18. Citation on PubMed or Free article on PubMed Central Krantz ID, McCallum J, DeScipio C, Kaur M, Gillis LA, ... doi: 10.1038/ng1364. Epub 2004 May 16. Citation on PubMed or Free article on PubMed ... V, Krantz ID, Musio A. Mutation spectrum and genotype-phenotype correlation ...
    https://medlineplus.gov/genetics/gene/nipbl - Genetics
  7. IDS gene 
    ... s00431-007-0635-4. Epub 2007 Nov 23. Citation on PubMed or Free article on PubMed Central
    https://medlineplus.gov/genetics/gene/ids - Genetics
  8. SMC1A gene 
    ... doi: 10.1086/511888. Epub 2007 Jan 17. Citation on PubMed or Free article on PubMed Central Deardorff MA, Noon SE, Krantz ID. Cornelia de Lange Syndrome. 2005 Sep 16 [updated ...
    https://medlineplus.gov/genetics/gene/smc1a - Genetics
  9. DRD5 gene 
    ... 2):162-6. doi: 10.1002/mds.21182. Citation on PubMed Gizer IR, Ficks C, Waldman ID. Candidate gene studies of ADHD: a meta-analytic review. Hum Genet. 2009 Jul;126(1):51-90. doi: 10.1007/s00439-009-0694-x. Epub 2009 Jun 9. Citation on PubMed Li D, Sham PC, Owen MJ, ...
    https://medlineplus.gov/genetics/gene/drd5 - Genetics
  10. NOTCH2 gene 
    ... 10.1002/humu.21546. Epub 2011 Sep 9. Citation on PubMed McDaniell R, Warthen DM, Sanchez-Lara PA, Pai A, Krantz ID, Piccoli DA, Spinner NB. NOTCH2 mutations cause Alagille ...
    https://medlineplus.gov/genetics/gene/notch2 - Genetics
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