Search Results - Pratt, V.M.

  • Showing 1 - 4 results of 4
Refine Results
  1. 1
    Duplication 6q21q23 in two unrelated patients

    Duplication 6q21q23 in two unrelated patients by Pratt, V.M., Roberson, J.R., Weiss, L., Van Dyke, D.L.

    Get full text
    Items that this one cites
    Article
    Save to List
    Saved in:
  2. 2
    DNA Studies of Limb-Girdle Muscular Dystrophy Type 2A in the Amish Exclude a Modifying Mitochondrial Gene and Show No Evidence for a Modifying Nuclear Gene

    DNA Studies of Limb-Girdle Muscular Dystrophy Type 2A in the Amish Exclude a Modifying Mitochondrial Gene and Show No Evidence for a Modifying Nuclear Gene by Pratt, V.M., Jackson, C.E., Wallace, D.C., Gurley, D.S., Feit, A., Feldman, G.L.

    Get full text
    Items that this one cites
    Items that cite this one
    Article
    Save to List
    Saved in:
  3. 3
    Linkage of a new mutation in the proteolipid protein (PLP) gene to Pelizaeus-Merzbacher disease (PMD) in a large Finnish kindred

    Linkage of a new mutation in the proteolipid protein (PLP) gene to Pelizaeus-Merzbacher disease (PMD) in a large Finnish kindred by PRATT, V. M, KIEFER, J. R, LÄHDETIE, J, SCHLEUTKER, J, HODES, M. E, DLOUHY, S. R

    Get full text
    Article
    Save to List
    Saved in:
  4. 4
    AhaII polymorphism in human X-linked proteolipid protein gene (PLP)

    AhaII polymorphism in human X-linked proteolipid protein gene (PLP) by Trofatter, J A, Pratt, V M, Dlouhy, S R, Hodes, M E

    Published in Nucleic acids research
    Get full text
    Article
    Save to List
    Saved in:

Search Tools: