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Results 1 - 10 of 13 for mode
  1. GNAI3 gene 
    ... S, Amiel J. Heterogeneity of mutational mechanisms and modes of inheritance in auriculocondylar syndrome. J Med Genet. ...
    https://medlineplus.gov/genetics/gene/gnai3 - Genetics
  2. PLCB4 gene 
    ... S, Amiel J. Heterogeneity of mutational mechanisms and modes of inheritance in auriculocondylar syndrome. J Med Genet. ...
    https://medlineplus.gov/genetics/gene/plcb4 - Genetics
  3. Miller syndrome 
    ... Genee-Wiedemann in a family--remarks on the mode of inheritance: report on two sibs. Am J ...
    https://medlineplus.gov/genetics/condition/miller-syndrome - Genetics
  4. Dihydropyrimidinase deficiency 
    ... Population and family studies of dihydropyrimidinuria: prevalence, inheritance mode, and risk of fluorouracil toxicity. Am J Med ...
    https://medlineplus.gov/.../condition/dihydropyrimidinase-deficiency - Genetics
  5. Hereditary hemochromatosis 
    ... and other factors such as genetic cause and mode of inheritance.Type 1, the most common form ...
    https://medlineplus.gov/.../condition/hereditary-hemochromatosis - Genetics
  6. Auriculo-condylar syndrome 
    ... S, Amiel J. Heterogeneity of mutational mechanisms and modes of inheritance in auriculocondylar syndrome. J Med Genet. ...
    https://medlineplus.gov/.../condition/auriculo-condylar-syndrome - Genetics
  7. Intrauterine growth restriction, metaphyseal dysplasia, adrenal hypoplasia congenita, and genital anomalies 
    ... IMAGe association: additional clinical variants and a proposed mode of inheritance. J Clin Endocrinol Metab. 2005 Jun; ...
    https://medlineplus.gov/...ypoplasia-congenita-and-genital-anomalies - Genetics
  8. DPYS gene 
    ... Population and family studies of dihydropyrimidinuria: prevalence, inheritance mode, and risk of fluorouracil toxicity. Am J Med ...
    https://medlineplus.gov/genetics/gene/dpys - Genetics
  9. Anhidrotic ectodermal dysplasia with immune deficiency 
    ... signs and symptoms and are distinguished by the modes of inheritance: X-linked recessive or autosomal dominant. ...
    https://medlineplus.gov/...todermal-dysplasia-with-immune-deficiency - Genetics
  10. OPA1 gene 
    ... P. OPA1-related disorders: Diversity of clinical expression, modes of inheritance and pathophysiology. Neurobiol Dis. 2016 Jun; ...
    https://medlineplus.gov/genetics/gene/opa1 - Genetics
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