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  1. MOCS2 gene: MedlinePlus Genetics 
    https://medlineplus.gov/genetics/gene/mocs2
    ... form of the disorder designated type B or complementation group B. The MOCS2 gene mutations involved in molybdenum cofactor deficiency likely eliminate the ...
  2. Fanconi Anemia - GeneReviews® - NCBI Bookshelf 
    https://www.ncbi.nlm.nih.gov/books/NBK1401
    ... FANCE 602774 RAD51 PARALOG C; RAD51C 602956 FANCG GENE; FANCG 603467 FANCONI ANEMIA, COMPLEMENTATION GROUP F; FANCF 604094 MITOTIC ARREST-DEFICIENT 2 LIKE 2; ...
  3. pdf2018NewHeadingsSingleColumn508.pdf 
    https://www.nlm.nih.gov/.../2018NewHeadingsSingleColumn508.pdf
    ... and stabilize these proteins at homologous recombination sites. Mutations in the PALB2 gene are associated with FANCONI ANEMIA complementation group N; type 3 PANCREATIC NEOPLASMS; and susceptibility to ...
  4. Zellweger Spectrum Disorder - GeneReviews® - NCBI Bookshelf 
    https://www.ncbi.nlm.nih.gov/books/NBK1448
    ... Moser HW, Suzuki Y, Kondo N, Fujiki Y. Mutations in novel peroxin gene PEX26 that cause peroxisome-biogenesis disorders of complementation group 8 provide a genotype-phenotype correlation. Am J ...
  5. MOCS1 gene: MedlinePlus Genetics 
    https://medlineplus.gov/genetics/gene/mocs1
    ... form of the disorder designated type A or complementation group A. This is the most common form of the condition, accounting for approximately two-thirds of cases. The MOCS1 gene mutations involved in molybdenum cofactor deficiency likely eliminate the ...
  6. Molybdenum cofactor deficiency: MedlinePlus Genetics 
    https://medlineplus.gov/.../condition/molybdenum-cofactor-deficiency
    ... disorder, named types A, B, and C (or complementation groups A, B, and C). The forms have the same signs and symptoms but are distinguished by their genetic cause: MOCS1 gene mutations cause type A, MOCS2 gene mutations cause type ...
  7. NLM Digital Collections - Report to the Medical Research Council on the Work of the Division of Molecular Genetics, now ... 
    Publication: Produced: November 1971
    resource.nlm.nih.gov/101584582X71
    ... theory which explains rather well the paucity of complementation groups in this and other organisms. We know that some single gene mutations can produce profound changes in the organisation of ...
  8. Fanconi anemia: MedlinePlus Genetics 
    https://medlineplus.gov/genetics/condition/fanconi-anemia
    ... COMPLEMENTATION GROUP A; FANCA FANCONI ANEMIA, COMPLEMENTATION GROUP F; ... GENE; FANCM FANCONI ANEMIA, COMPLEMENTATION GROUP G; FANCG FANCONI ...
  9. Xeroderma pigmentosum: MedlinePlus Genetics 
    https://medlineplus.gov/genetics/condition/xeroderma-pigmentosum
    ... Disorders (NORD) Clinical Trials ClinicalTrials.gov ... GROUP F; XPF XERODERMA PIGMENTOSUM, COMPLEMENTATION GROUP G; XPG XERODERMA ...
  10. ERCC8 gene: MedlinePlus Genetics 
    https://medlineplus.gov/genetics/gene/ercc8
    ... syndrome. Additionally, it is unknown why the Trp361Cys mutation causes photosensitivity without the ... group 8 excision repair cross-complementing rodent repair deficiency, ...
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