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Results 1 - 7 of 7 for Complementation
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  1. Fanconi anemia 
    ... Registry: Fanconi anemia Genetic Testing Registry: Fanconi anemia, complementation group M Genetic Testing Registry: Fanconi anemia complementation group A Genetic Testing Registry: Fanconi anemia complementation ...
    https://medlineplus.gov/genetics/condition/fanconi-anemia - Genetics
  2. Xeroderma pigmentosum 
    ... at least eight genetic forms of xeroderma pigmentosum: complementation group A (XP-A) through complementation group G (XP-G), plus a variant type ( ... for Rare Disorders (NORD) ClinicalTrials.gov XERODERMA PIGMENTOSUM, COMPLEMENTATION GROUP A; XPA XERODERMA PIGMENTOSUM, COMPLEMENTATION GROUP C; ...
    https://medlineplus.gov/genetics/condition/xeroderma-pigmentosum - Genetics
  3. Molybdenum cofactor deficiency 
    ... disorder, named types A, B, and C (or complementation groups A, B, and C). The forms have ... Rare Disorders (NORD) ClinicalTrials.gov MOLYBDENUM COFACTOR DEFICIENCY, COMPLEMENTATION GROUP A; MOCODA MOLYBDENUM COFACTOR DEFICIENCY, COMPLEMENTATION GROUP ...
    https://medlineplus.gov/.../condition/molybdenum-cofactor-deficiency - Genetics
  4. Bare lymphocyte syndrome type II 
    ... Genetic Testing Registry: Bare lymphocyte syndrome type 2, complementation group A Genetic Testing Registry: Bare lymphocyte syndrome, type II, complementation group c Immunodeficiency by defective expression of MHC ...
    https://medlineplus.gov/.../bare-lymphocyte-syndrome-type-ii - Genetics
  5. Homocystinuria 
    ... 10)-METHYLENETETRAHYDROFOLATE REDUCTASE ACTIVITY HOMOCYSTINURIA-MEGALOBLASTIC ANEMIA, cblE COMPLEMENTATION TYPE; HMAE METHYLMALONIC ACIDURIA AND HOMOCYSTINURIA, cblD TYPE; ...
    https://medlineplus.gov/genetics/condition/homocystinuria - Genetics
  6. Pyruvate dehydrogenase deficiency 
    ... two brothers and restoration of activity by protein complementation. J Clin Endocrinol Metab. 2005 Jul;90(7): ...
    https://medlineplus.gov/.../pyruvate-dehydrogenase-deficiency - Genetics
  7. UV-sensitive syndrome 
    ... is distinct from xeroderma pigmentosum variant and rodent complementation group I. Am J Hum Genet. 1995 Jun; ...
    https://medlineplus.gov/genetics/condition/uv-sensitive-syndrome - Genetics