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Results 21 - 29 of 29 for Grange syndrome
  1. 1q21.1 microdeletion 
    ... Obersztyn E, Nowakowska B, Rosengren SS, Bader PI, Grange DK, Naqvi S, Garnica AD, Bernes SM, Fong ...
    https://medlineplus.gov/genetics/condition/1q211-microdeletion - Genetics
  2. Hypohidrotic ectodermal dysplasia 
    ... 1):97-107. Citation on PubMed Wright JT, Grange DK, Fete M. Hypohidrotic Ectodermal Dysplasia. 2003 Apr ...
    https://medlineplus.gov/.../hypohidrotic-ectodermal-dysplasia - Genetics
  3. GLI3 gene 
    ... Dinulos MB, Flannery DB, Fox MA, Graham JM, Grange DK, Guttmacher AE, Hannibal MC, Henn W, Hennekam ...
    https://medlineplus.gov/genetics/gene/gli3 - Genetics
  4. 1q21.1 microduplication 
    ... Disorders (NORD) ClinicalTrials.gov ... S, Geragthy MT, Innis JW, Obersztyn E, Nowakowska B, Rosengren SS, Bader PI, Grange DK, Naqvi S, Garnica AD, Bernes SM, Fong ...
    https://medlineplus.gov/genetics/condition/1q211-microduplication - Genetics
  5. Chromosome 1 
    ... Obersztyn E, Nowakowska B, Rosengren SS, Bader PI, Grange DK, Naqvi S, Garnica AD, Bernes SM, Fong ...
    https://medlineplus.gov/genetics/chromosome/1 - Genetics
  6. Chromosome 20 
    ... 1.225. No abstract available. Citation on PubMed Grange DK, Garcia-Heras J, Kilani RA, Lamp S. ...
    https://medlineplus.gov/genetics/chromosome/20 - Genetics
  7. IDH2 gene 
    ... NR, Das AM, de Klerk JB, Feigenbaum AS, Grange DK, Hofstede FC, Holme E, Kirk EP, Korman ... spindle cell hemangioma in Ollier disease and Maffucci syndrome. Nat Genet. 2011 Nov 6;43(12):1256- ...
    https://medlineplus.gov/genetics/gene/idh2 - Genetics
  8. MTOR gene 
    ... Bowling KM, Mei D, Conti V, de la Grange P, Ferrand-Sorbets S, Dorfmuller G, Lambrecq V, ... Li Y, Yigit G, Wollnik B. Smith-Kingsmore syndrome: A third family with the MTOR mutation c. ...
    https://medlineplus.gov/genetics/gene/mtor - Genetics
  9. KCNQ1OT1 gene 
    ... Thomassin H, Pandey RR, Kanduri M, Gondor A, Grange T, Ohlsson R, Kanduri C. An antisense RNA ... Squire J. Tumor development in the Beckwith-Wiedemann syndrome is associated with a variety of constitutional molecular ...
    https://medlineplus.gov/genetics/gene/kcnq1ot1 - Genetics
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