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Results 1 - 10 of 76 for Canada
  1. GCDH gene 
    ... 5) is prevalent in the Ojibwa population of Canada. As a result of this mutation, an abnormally ... acidemia type 1 in Manitoba and northwestern Ontario, Canada. Mol Genet Metab. 2002 Jan;75(1):70- ...
    https://medlineplus.gov/genetics/gene/gcdh - Genetics
  2. How can I find a genetics professional in my area?: MedlinePlus Genetics 
    ... of genetic counselors in the United States and Canada . You can search by location, name, area of ... has a searchable directory of genetic counselors in Canada . You can search by name, distance from an ...
    https://medlineplus.gov/.../consult/findingprofessional - Genetics
  3. Megalencephaly-polymicrogyria-polydactyly-hydrocephalus syndrome 
    ... N, Wieczorek D, Steinraths M, Majewski J; FORGE Canada Consortium; Boycot KM, Pilz DT, Ross ME, Dobyns ... Beaulieu CL; Finding of Rare Disease Genes (FORGE) Canada Consortium; Majewski J, Bulman DE, O'Driscoll M, ...
    https://medlineplus.gov/...ogyria-polydactyly-hydrocephalus-syndrome - Genetics
  4. AGL gene 
    ... with glycogen storage disease type III from Germany, Canada, Afghanistan, Iran, and Turkey. J Hum Genet. 2006; ...
    https://medlineplus.gov/genetics/gene/agl - Genetics
  5. EFTUD2 gene 
    ... AW, Lohmann DR, Hehr U, Bohm D; FORGE Canada Consortium; Majewski J, Bulman DE, Wieczorek D, Boycott ...
    https://medlineplus.gov/genetics/gene/eftud2 - Genetics
  6. D-bifunctional protein deficiency 
    ... SE, Mackenzie A, Beaulieu CL, Mooyer PA; FORGE Canada Consortium; Wanders RJ, Majewski J, Bulman DE, Geraghty ...
    https://medlineplus.gov/.../d-bifunctional-protein-deficiency - Genetics
  7. Hypophosphatasia 
    ... particularly frequent in a Mennonite population in Manitoba, Canada, where about 1 in 2,500 infants is ...
    https://medlineplus.gov/genetics/condition/hypophosphatasia - Genetics
  8. Autosomal recessive spastic ataxia of Charlevoix-Saguenay 
    ... first seen, the Charlevoix-Saguenay region of Quebec, Canada, ARSACS has been identified in individuals worldwide. The ...
    https://medlineplus.gov/...ive-spastic-ataxia-of-charlevoix-saguenay - Genetics
  9. Autosomal dominant cerebellar ataxia, deafness, and narcolepsy 
    ... L, Smith A, Pare G, Ainsworth P; Care4Rare Canada Consortium; Boycott KM, Warman-Chardon J, Sadikovic B. ...
    https://medlineplus.gov/...cerebellar-ataxia-deafness-and-narcolepsy - Genetics
  10. SRCAP gene 
    ... DR, Chudley AE, Chodirker BN, Marcadier J; FORGE Canada Consortium; Majewski J, Bulman DE, White SM, Boycott ...
    https://medlineplus.gov/genetics/gene/srcap - Genetics
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