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200 results
  1. Methods - Testing of CYP2C19 Variants and Platelet Reactivity for Guiding Antiplatelet Treatment - NCBI Bookshelf 
    https://www.ncbi.nlm.nih.gov/books/NBK236986
    ... case of biallelic loci dominant, recessive, additive, or co-dominant genetic models of inheritance are possible. Inferences under ...
  2. von Willebrand Disease - GeneReviews® - NCBI Bookshelf 
    https://www.ncbi.nlm.nih.gov/books/NBK7014
    ... type 3 von Willebrand disease: further evidence for co-dominant inheritance of mutant alleles. J Thromb Haemost. 2013; ...
  3. Alpha-1 Antitrypsin Deficiency - GeneReviews® - NCBI Bookshelf 
    https://www.ncbi.nlm.nih.gov/books/NBK1519
    ... antitrypsin deficiency (AATD) is inherited in an autosomal co-dominant manner. Risk to Family Members Parents of a ...
  4. Managing non-muscle-invasive bladder cancer - Bladder Cancer - NCBI Bookshelf 
    https://www.ncbi.nlm.nih.gov/books/NBK356304
    ... in patients aged ≤55 years old regardless of co-morbid status. For patients ≥70 years old, conservative therapy was either dominant or had an ICER that was likely to ...
  5. Cantú syndrome: MedlinePlus Genetics 
    https://medlineplus.gov/genetics/condition/cantu-syndrome
    ... 1002/(sici)1096-8628(19970317)69:23.0.co;2-l. Citation on PubMed Grange DK, Lorch SM, Cole PL, Singh GK. Cantu syndrome in a woman and her two daughters: Further confirmation of autosomal dominant inheritance and review of the cardiac manifestations. Am ...
  6. EBP gene: MedlinePlus Genetics 
    https://medlineplus.gov/genetics/gene/ebp
    ... 10.1002/1096-8628(20001002)94:43.0.co;2-3. Citation on PubMed Milunsky JM, Maher TA, Metzenberg AB. Molecular, biochemical, and phenotypic analysis of a hemizygous male with a severe atypical phenotype for X-linked dominant Conradi-Hunermann-Happle syndrome and a mutation in ...
  7. Huntington Disease-Like 2 - GeneReviews® - NCBI Bookshelf 
    https://www.ncbi.nlm.nih.gov/books/NBK1529
    ... Huntington disease (HD), and is based on the co-occurrence of: (1) movement abnormalities (chorea, dystonia, and/or parkinsonism) reflecting basal ganglia dysfunction, dementia, and psychiatric disturbances; and (2) autosomal dominant inheritance. The most obvious diagnosis to exclude is ...
  8. Oculofaciocardiodental syndrome: MedlinePlus Genetics 
    https://medlineplus.gov/.../oculofaciocardiodental-syndrome
    ... 1002/(SICI)1096-8628(19960503)63:13.0.CO;2-G. Citation on PubMed Hedera P, Gorski JL. Oculo-facio-cardio-dental syndrome: skewed X chromosome inactivation in mother and daughter suggest X-linked dominant Inheritance. Am J Med Genet A. 2003 Dec ...
  9. Autosomal Dominant Robinow Syndrome - GeneReviews® - NCBI Bookshelf 
    https://www.ncbi.nlm.nih.gov/books/NBK268648
    ... 2454 Email: office@restrictedgrowth.co.uk www.restrictedgrowth.co.uk ... Dominant Robinow Syndrome: Genes and Databases View in own ...
  10. Genetics of Prostate Cancer (PDQ®) - PDQ Cancer Information Summaries - NCBI Bookshelf 
    https://www.ncbi.nlm.nih.gov/books/NBK65784
    ... linkage analysis, which searches for genetic risk variants co-segregating ... dominant, autosomal recessive , X-linked, and mitochondrial). GWAS, on ...
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