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Results 1 - 10 of 177 for bps
  1. TRIP13 gene 
    ... early development. More About This Health Condition 16E1-BP 16E1BP HPV16 E1 protein binding protein human papillomavirus ...
    https://medlineplus.gov/genetics/gene/trip13 - Genetics
  2. DYRK1A gene 
    ... Levy R, O'Day DR, Krumm N, Coe BP, Martin BK, Borenstein E, Nickerson DA, Mefford HC, ... L, Girirajan S, Karakoc E, Krumm N, Coe BP, Levy R, Ko A, Lee C, Smith JD, ...
    https://medlineplus.gov/genetics/gene/dyrk1a - Genetics
  3. X-linked infantile nystagmus 
    ... RC, Aamir A, Sano R, Jin J, Brooks BP, Kohl S, Arveiler B, Montoliu L, Engle EC, ... M, Lindsay S, Kumar A, Araki M, Leroy BP, McLean RJ, Sheth V, Maconachie G, Thomas S, ...
    https://medlineplus.gov/.../condition/x-linked-infantile-nystagmus - Genetics
  4. 7q11.23 duplication syndrome 
    ... 1. Citation on PubMed Mervis CB, Klein-Tasman BP, Huffman MJ, Velleman SL, Pitts CH, Henderson DR, ... PubMed Central Mervis CB, Morris CA, Klein-Tasman BP, Velleman SL, Osborne LR. 7q11.23 Duplication Syndrome. ...
    https://medlineplus.gov/.../condition/7q1123-duplication-syndrome - Genetics
  5. TH gene 
    ... L, Wessel J, Zhang K, Wen G, Kennedy BP, Rana BK, Das M, Rodriguez-Flores JL, Smith ... L, Wessel J, Zhang K, Wen G, Kennedy BP, Rana BK, Das M, Rodriguez-Flores JL, Smith ...
    https://medlineplus.gov/genetics/gene/th - Genetics
  6. ADNP syndrome 
    ... PubMed Helsmoortel C, Vulto-van Silfhout AT, Coe BP, Vandeweyer G, Rooms L, van den Ende J, ... Van Dijck A, Vulto-van Silfhout AT, Coe BP, Bernier R, Gerdts J, Rooms L, van den ...
    https://medlineplus.gov/genetics/condition/adnp-syndrome - Genetics
  7. Genetic epilepsy with febrile seizures plus 
    ... EH, Baulac S, Moller RS, Hjalgrim H, Koeleman BP; EuroEPINOMICS RES Consortium; Jurkat-Rott K, Lehman-Horn ... Nieuwenhuizen O, Lindhout D, George AL Jr, Koeleman BP, Rook MB. Nav 1.1 dysfunction in genetic ...
    https://medlineplus.gov/...netic-epilepsy-with-febrile-seizures-plus - Genetics
  8. 16p12.2 microdeletion 
    ... Epub 2015 Jul 8. Citation on PubMed Coe BP, Girirajan S, Eichler EE. The genetic variability and ... A, Weaver DD, Mark PR, Dickerson J, Garg BP, Ellingwood SA, Smith R, Banks VC, Smith W, ...
    https://medlineplus.gov/genetics/condition/16p122-microdeletion - Genetics
  9. KCNH2 gene 
    ... J, Elayi CS, Bartos DC, Burgess DE, Delisle BP. Mechanistic basis for type 2 long QT syndrome ... CL, Burgess DE, Elayi CS, January CT, Delisle BP. Molecular pathogenesis of long QT syndrome type 2. ...
    https://medlineplus.gov/genetics/gene/kcnh2 - Genetics
  10. FOXL2 gene 
    ... V, Laframboise R, Laissue P, Leppig K, Leroy BP, Miller DT, Mowat D, Neumann L, Plomp A, ... Citation on PubMed Beysen D, Raes J, Leroy BP, Lucassen A, Yates JR, Clayton-Smith J, Ilyina ...
    https://medlineplus.gov/genetics/gene/foxl2 - Genetics
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