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Results 1 - 9 of 9 for PM 102
  1. Epidermolytic hyperkeratosis 
    ... CC, DiGiovanna JJ, Bale SJ, Marekov LN, Steinert PM, Compton JG. Mutations in the H1 and 1A domains in the keratin 1 gene in epidermolytic hyperkeratosis. J Invest Dermatol. 1994 Jan;102(1):17-23. doi: 10.1111/1523-1747. ...
    https://medlineplus.gov/.../condition/epidermolytic-hyperkeratosis - Genetics
  2. Greig cephalopolysyndactyly syndrome 
    ... hmg/8.9.1769. Citation on PubMed Kroisel PM, Petek E, Wagner K. Phenotype of five patients with Greig syndrome and microdeletion of 7p13. Am J Med Genet. 2001 Aug 15;102(3):243-9. doi: 10.1002/ajmg.1443. ...
    https://medlineplus.gov/.../greig-cephalopolysyndactyly-syndrome - Genetics
  3. Gestational diabetes 
    ... Res Clin Obstet Gynaecol. 2015 Jan;29(1):102-9. doi: 10.1016/j.bpobgyn.2014.08.008. Epub 2014 Aug 26. Citation on PubMed Catalano PM. The impact of gestational diabetes and maternal obesity ...
    https://medlineplus.gov/genetics/condition/gestational-diabetes - Genetics
  4. Cold-induced sweating syndrome 
    ... In: Am J Hum Genet. 2018 Apr 5;102(4):713. Citation on PubMed or Free article ... on PubMed Central Hahn AF, Jones DL, Knappskog PM, Boman H, McLeod JG. Cold-induced sweating syndrome: ...
    https://medlineplus.gov/.../condition/cold-induced-sweating-syndrome - Genetics
  5. Autosomal recessive congenital stationary night blindness 
    ... Acad Sci U S A. 2005 Mar 29;102(13):4884-9. doi: 10.1073/pnas.0501233102. ... S, Baba K, Tosini G, Pozdeyev N, Iuvone PM, Bojang P Jr, Pearring JN, Simonsz HJ, van ...
    https://medlineplus.gov/...ive-congenital-stationary-night-blindness - Genetics
  6. Pseudocholinesterase deficiency 
    ... prolonged neuromuscular block after succinylcholine. Anesthesiology. 2005 Mar;102(3):531-5. doi: 10.1097/00000542-200503000- ... T, Nightingale BN, Burns JC, Sullivan DR, Stewart PM. Butyrylcholinesterase (BCHE) genotyping for post-succinylcholine apnea in ...
    https://medlineplus.gov/.../pseudocholinesterase-deficiency - Genetics
  7. 16p11.2 duplication 
    ... locus. Nature. 2011 Aug 31;478(7367):97-102. doi: 10.1038/nature10406. Citation on PubMed or ...
    https://medlineplus.gov/genetics/condition/16p112-duplication - Genetics
  8. Warfarin sensitivity 
    ... Dosing: 2017 Update. Clin Pharmacol Ther. 2017 Sep;102(3):397-404. doi: 10.1002/cpt.668. ...
    https://medlineplus.gov/genetics/condition/warfarin-sensitivity - Genetics
  9. Combined oxidative phosphorylation deficiency 1 
    ... GFM1 mutations. Front Genet. 2015 Mar 23;6:102. doi: 10.3389/fgene.2015.00102. eCollection 2015. ... PubMed Central Smits P, Antonicka H, van Hasselt PM, Weraarpachai W, Haller W, Schreurs M, Venselaar H, ...
    https://medlineplus.gov/...ed-oxidative-phosphorylation-deficiency-1 - Genetics