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Results 1 - 10 of 25 for map
  1. FG syndrome 
    ... A, Moraine C. A gene for FG syndrome maps in the Xq12-q21.31 region. Am J ... heterogeneity of FG syndrome: a fourth locus (FGS4) maps to Xp11.4-p11.3 in an Italian ...
    https://medlineplus.gov/genetics/condition/fg-syndrome - Genetics
  2. Hyperprolinemia 
    ... the Drosophila melanogaster sluggish-A (proline oxidase) gene maps to 22q11.2, and is a candidate gene ...
    https://medlineplus.gov/genetics/condition/hyperprolinemia - Genetics
  3. Distal 18q deletion syndrome 
    ... resolution array CGH: an update of the phenotypic map. Am J Med Genet A. 2007 Aug 15; ...
    https://medlineplus.gov/.../condition/distal-18q-deletion-syndrome - Genetics
  4. 1p36 deletion syndrome 
    ... CD, Bacino CA, Shapira SK, Shaffer LG. Physical map of 1p36, placement of breakpoints in monosomy 1p36, ...
    https://medlineplus.gov/genetics/condition/1p36-deletion-syndrome - Genetics
  5. Horizontal gaze palsy with progressive scoliosis 
    ... RW. Familial horizontal gaze palsy with progressive scoliosis maps to chromosome 11q23-25. Neurology. 2002 Aug 13; ...
    https://medlineplus.gov/...tal-gaze-palsy-with-progressive-scoliosis - Genetics
  6. Spastic paraplegia type 8 
    ... Brazilian family with pure autosomal dominant spastic paraplegia maps to 8q: analysis of muscle beta 1 syntrophin. ...
    https://medlineplus.gov/genetics/condition/spastic-paraplegia-type-8 - Genetics
  7. Isolated Duane retraction syndrome 
    ... Duane's retraction syndrome as a dominant trait map to the DURS2 genetic locus. Invest Ophthalmol Vis ...
    https://medlineplus.gov/.../isolated-duane-retraction-syndrome - Genetics
  8. Weyers acrofacial dysostosis 
    ... dominant postaxial polydactyly, nail dystrophy, and dental abnormalities map to chromosome 4p16, in the region containing the ...
    https://medlineplus.gov/.../condition/weyers-acrofacial-dysostosis - Genetics
  9. CHMP2B-related frontotemporal dementia 
    ... Hardy J, Collinge J. Familial non-specific dementia maps to chromosome 3. Hum Mol Genet. 1995 Sep; ...
    https://medlineplus.gov/.../chmp2b-related-frontotemporal-dementia - Genetics
  10. Congenital cataracts, facial dysmorphism, and neuropathy 
    ... CCFDN) syndrome: a novel developmental disorder in Gypsies maps to 18qter. Eur J Hum Genet. 1999 Jul; ...
    https://medlineplus.gov/...taracts-facial-dysmorphism-and-neuropathy - Genetics
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