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8 results
  1. pdf2019NewMeShHeadingsSingleColumn.pdf 
    https://www.nlm.nih.gov/.../2019NewMeShHeadingsSingleColumn.pdf
    ... also used in the treatment of rapidly progressing AUTOSOMAL DOMINANT POLYCYSTIC KIDNEY DISEASE to slow the rate of cyst development and ...
  2. pdf2019NewMeShHeadings.pdf 
    https://www.nlm.nih.gov/mesh/2019/download/2019NewMeShHeadings.pdf
    ... also used in the treatment of rapidly progressing AUTOSOMAL DOMINANT POLYCYSTIC KIDNEY DISEASE to slow the rate of cyst development and ...
  3. pdf2018MeShTreeHierarchy.pdf 
    https://www.nlm.nih.gov/mesh/2018/download/2018MeShTreeHierarchy.pdf
    ... Pelger-Huet Anomaly C16.320.798...........................................Polycystic Kidney Diseases C16.320.798.500...........................................Polycystic Kidney, Autosomal Dominant C16.320.798.510...........................................Polycystic Kidney, Autosomal Recessive ...
  4. pdfNLM Technical Bulletin, no.129-140 
    https://www.nlm.nih.gov/.../nlmarchives/techbull/129-140-1980.pdf
    ... XU ENCEPHALITIS VIRUS. ST. LOUIS XU KYASANUR FOREST DISEASE VIRUS XU LANOAT VIRUS FROGS AND ... An autosomal dominant diaeaae featuring multiple colonlc polyposis with malignant tendency, ...
  5. pdfNLM Technical Bulletin, no.117-128 
    https://www.nlm.nih.gov/.../nlmarchives/techbull/117-128-1979.pdf
    ... 440 E5 478 610 500 X BROAD BETA DISEASE X ... G4 610 555 412 an autosomal dominant trait The theory that T-cells monitor cell ...
  6. pdfNLM Annual Report of Programs and Services, 1980 
    https://www.nlm.nih.gov/.../nlmarchives/annualreport/1980.pdf
    ... A. McKusick: Mendelian Inheritance in Man: Catalog of Autosomal Dominant, Autosomal Recessive and X-linked Phenotypes, 5th ed., Baltimore, ...
  7. pdfNational Library of Medicine Programs and Services FY2014 
    https://www.nlm.nih.gov/ocpl/anreports/fy2014.pdf
    ... a study involving genetic counseling for carriers of autosomal recessive genetic diseases. Beginning in July 2014, GHR implemented a customer ... RCSB Research Collaboratory for Structural Bioinformatics RDMS Rare Disease ... Reference Sequence (database) RefSNP Reference SNP (database) RELACIGER Red ...
  8. MEDLINE Data Changes - 2007. NLM Technical Bulletin. 2006 Nov–Dec 
    https://www.nlm.nih.gov/.../nd06/nd06_medline_data_changes2007.html
    ... Regulating Neutral Endopeptidase/deficiency Hypophosphatemic Rickets, X-Linked Dominant Transforming Growth Factor beta1/deficiency Camurati-Engelmann Syndrome alpha-Galactosidase/deficiency Fabry Disease Additional Changes to MEDLINE and OLDMEDLINE Data 1. ...