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Results 1 - 10 of 114 for PMS
  1. ... PubMed AQUAPORIN 2; AQP2 NCBI Gene ClinVar Deen PM, Verdijk MA, Knoers NV, Wieringa B, Monnens LA, ... science.8140421. Citation on PubMed Knoers NV, Deen PM. Molecular and cellular defects in nephrogenic diabetes insipidus. ...
  2. ... NCBI Gene ClinVar Hahn AF, Jones DL, Knappskog PM, Boman H, McLeod JG. Cold-induced sweating syndrome: ... PH, Bamforth JS, Miles JH, McLeod JG, Knappskog PM, Boman H. Cold-induced sweating syndrome: CISS1 and ...
  3. ... Citation on PubMed Hahn AF, Jones DL, Knappskog PM, Boman H, McLeod JG. Cold-induced sweating syndrome: ... PH, Bamforth JS, Miles JH, McLeod JG, Knappskog PM, Boman H. Cold-induced sweating syndrome: CISS1 and ...
  4. ... 22. No abstract available. Citation on PubMed Elias PM, Williams ML, Crumrine D, Schmuth M. Inherited disorders ... M, Moskowitz DG, Christiano AM, Feingold KR, Elias PM. Structural and functional consequences of loricrin mutations in ...
  5. ... S, Boerkoel CF, Sicolo N, Martin M, Nishina PM, Naggert JK. Mutations in ALMS1 cause obesity, type ... GB, Hopkinson I, Sicolo N, Naggert JK, Nishina PM. New Alstrom syndrome phenotypes based on the evaluation ...
  6. ... A, Krause MP, Abad C, Tekin M, Neilsen PM, Callen DF, Scherer SW, Keller GM, Kaplan DR, ... Epub 2014 Nov 20. Citation on PubMed Neilsen PM, Cheney KM, Li CW, Chen JD, Cawrse JE, ...
  7. ... N, Bale SJ, DiGiovanna JJ, Compton JG, Steinert PM. A leucine----proline mutation in the H1 subdomain ... CC, DiGiovanna JJ, Bale SJ, Marekov LN, Steinert PM, Compton JG. Mutations in the H1 and 1A ...
  8. ... JI, Kanakura Y, Kohara N, Schrezenmeier H, Krawitz PM, Kinoshita T. Complement and inflammasome overactivation mediates paroxysmal ... doi: 10.1172/JCI123501. Citation on PubMed Krawitz PM, Hochsmann B, Murakami Y, Teubner B, Kruger U, ...
  9. ... Xie M, Vulto I, Phillips JA 3rd, Lansdorp PM, Greider CW, Loyd JE. Telomerase mutations in families ... H, Kajigaya S, Baerlocher GM, Chanock SJ, Lansdorp PM, Young NS. Mutations in TERT, the gene for ...
  10. ... 8; CMM8 NCBI Gene ClinVar Amiel J, Watkin PM, Tassabehji M, Read AP, Winter RM. Mutation of ... abstract available. Citation on PubMed Smith SD, Kelley PM, Kenyon JB, Hoover D. Tietz syndrome (hypopigmentation/deafness) ...
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