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Results 1 - 10 of 24 for Pps
  1. Gout 
    ... on PubMed Central Khanna D, Fitzgerald JD, Khanna PP, Bae S, Singh MK, Neogi T, Pillinger MH, ... Free article on PubMed Central Khanna D, Khanna PP, Fitzgerald JD, Singh MK, Bae S, Neogi T, ...
    https://medlineplus.gov/genetics/condition/gout - Genetics
  2. Popliteal pterygium syndrome 
    ... to cause the disorder. Facio-genito-popliteal syndrome PPS Genetic Testing Registry: Popliteal pterygium syndrome National Organization for Rare Disorders (NORD) POPLITEAL PTERYGIUM SYNDROME; PPS PubMed Ghassibe M, Revencu N, Bayet B, Gillerot ...
    https://medlineplus.gov/.../condition/popliteal-pterygium-syndrome - Genetics
  3. Short/branched chain acyl-CoA dehydrogenase deficiency 
    ... Epub 2006 Sep 6. Citation on PubMed Madsen PP, Kibaek M, Roca X, Sachidanandam R, Krainer AR, ... M, Berry SA, Rinaldo P, Whitley CB, Madsen PP, van Calcar SC, Lussky RC, Andresen BS, Wolff ...
    https://medlineplus.gov/...d-chain-acyl-coa-dehydrogenase-deficiency - Genetics
  4. ALG12-congenital disorder of glycosylation 
    ... by a deficiency in dolichyl-P-mannose:Man7GlcNAc2-PP-dolichyl mannosyltransferase. J Biol Chem. 2002 Jul 12; ... Korner C. Deficiency of dolichyl-P-Man:Man7GlcNAc2-PP-dolichyl mannosyltransferase causes congenital disorder of glycosylation type ...
    https://medlineplus.gov/...lg12-congenital-disorder-of-glycosylation - Genetics
  5. Acute promyelocytic leukemia 
    ... 8674(91)90113-d. Citation on PubMed Pandolfi PP. Oncogenes and tumor suppressors in the molecular pathogenesis ... 8.1379. Citation on PubMed Salomoni P, Pandolfi PP. The role of PML in tumor suppression. Cell. ...
    https://medlineplus.gov/.../condition/acute-promyelocytic-leukemia - Genetics
  6. Multiple familial trichoepithelioma 
    ... Citation on PubMed Zhang XJ, Liang YH, He PP, Yang S, Wang HY, Chen JJ, Yuan WT, ...
    https://medlineplus.gov/.../multiple-familial-trichoepithelioma - Genetics
  7. Trichorhinophalangeal syndrome type II 
    ... Superti-Furga A, Moreira LM, Santo LD, Schiper PP, Carvalho JH, Giedion A. Long-term follow-up ...
    https://medlineplus.gov/.../trichorhinophalangeal-syndrome-type-ii - Genetics
  8. CHMP2B-related frontotemporal dementia 
    ... Pooter T, Peeters K, Santens P, De Deyn PP, Fisher EM, Collinge J, Isaacs AM, Van Broeckhoven ...
    https://medlineplus.gov/.../chmp2b-related-frontotemporal-dementia - Genetics
  9. Cowden syndrome 
    ... N, Liu J, Wei W, Eng C, Pandolfi PP. WWP1 Gain-of-Function Inactivation of PTEN in ...
    https://medlineplus.gov/genetics/condition/cowden-syndrome - Genetics
  10. Rheumatoid arthritis 
    ... M, Seldin MF, Shadick NA, Steer S, Tak PP, Thomson W, van der Helm-van Mil AH, ...
    https://medlineplus.gov/genetics/condition/rheumatoid-arthritis - Genetics
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