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Results 1 - 10 of 76 for robert syndrome 16
  1. PRKAG2 gene 
    ... Lozado R, Shah G, Fananapazir L, Bachinski LL, Roberts R. Identification of a gene responsible for familial Wolff-Parkinson-White syndrome. N Engl J Med. 2001 Jun 14;344(24):1823-31. doi: 10.1056/NEJM200106143442403. Erratum In: N Engl J Med 2001 Aug 16;345(7):552. Hassan AS [corrected to Ali ...
    https://medlineplus.gov/genetics/gene/prkag2 - Genetics
  2. Wolff-Parkinson-White syndrome 
    ... Lozado R, Shah G, Fananapazir L, Bachinski LL, Roberts R. Identification of a gene responsible for familial Wolff-Parkinson-White syndrome. N Engl J Med. 2001 Jun 14;344(24):1823-31. doi: 10.1056/NEJM200106143442403. Erratum In: N Engl J Med 2001 Aug 16;345(7):552. Hassan AS [corrected to Ali ...
    https://medlineplus.gov/.../condition/wolff-parkinson-white-syndrome - Genetics
  3. Roberts syndrome 
    ... Zou H, Jabs EW. The molecular mechanism underlying Roberts syndrome involves loss of ... cohesion. Mol Biol Cell. 2005 Aug;16(8):3908-18. doi: 10.1091/mbc.e04- ...
    https://medlineplus.gov/genetics/condition/roberts-syndrome - Genetics
  4. ESCO2 gene 
    ... Zou H, Jabs EW. The molecular mechanism underlying Roberts syndrome involves loss of ... cohesion. Mol Biol Cell. 2005 Aug;16(8):3908-18. doi: 10.1091/mbc.e04- ...
    https://medlineplus.gov/genetics/gene/esco2 - Genetics
  5. PTPN11 gene 
    ... j.gde.2006.12.011. Epub 2007 Jan 16. Citation on PubMed Romano AA, Allanson JE, Dahlgren J, Gelb BD, Hall B, Pierpont ME, Roberts AE, Robinson W, Takemoto CM, Noonan JA. Noonan syndrome: clinical features, diagnosis, and management guidelines. Pediatrics. 2010 ...
    https://medlineplus.gov/genetics/gene/ptpn11 - Genetics
  6. NRAS gene 
    ... Int J Cancer. 2009 Jan 1;124(1):16-26. doi: 10.1002/ijc.23876. Citation on PubMed Romano AA, Allanson JE, Dahlgren J, Gelb BD, Hall B, Pierpont ME, Roberts AE, Robinson W, Takemoto CM, Noonan JA. Noonan syndrome: clinical features, diagnosis, and management guidelines. Pediatrics. 2010 ...
    https://medlineplus.gov/genetics/gene/nras - Genetics
  7. 16p11.2 deletion syndrome 
    ... a deletion of a small piece of chromosome 16. The deletion occurs near the middle of the ... kilobases (kb), at position p11.2 on chromosome 16. This deletion affects one of the two copies ...
    https://medlineplus.gov/genetics/condition/16p112-deletion-syndrome - Genetics
  8. 16p11.2 duplication 
    ... a small amount of genetic material within chromosome 16 is abnormally copied (duplicated). The duplication occurs near ... material on the short (p) arm of chromosome 16 at a position known as p11.2. This ...
    https://medlineplus.gov/genetics/condition/16p112-duplication - Genetics
  9. National Institute of Environmental Health Sciences (National Institute of Environmental Health Sciences)  
    ... DNA Damage, Hormonal Signaling, and Breast Cancer September 16 - From Cells to Society: Protecting Children and Pregnant ... 2022 - Tracking Nanoparticles Across the Placental Barrier June 16, 2022 - Fleshing Out a Fungal Toxin’s Role in ...
    https://www.niehs.nih.gov - Other Resources
  10. Progressive external ophthalmoplegia 
    ... doi: 10.1074/jbc.M506762200. Epub 2005 Jul 16. Citation on PubMed Cohen BH, Chinnery PF, Copeland WC. POLG-Related Disorders. 2010 Mar 16 [updated 2024 Feb 29]. In: Adam MP, Feldman ...
    https://medlineplus.gov/.../progressive-external-ophthalmoplegia - Genetics
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