Resumos publicados em anais de congressos internacionais

  1. M.Araujo, V.P.Forrer, E.C.Guilherme, C.F.Ramos, S.B.Farah, G.Guerra Jr e M.P.Mello, ``Molecular Studies On The 21- Hydroxylase Gene Cluster In Brazilian Families'', The 1994 Miami Bio/Tech. Winter Symp: Mol. Biol. of Human Diseases, Estados Unidos, 1, (1994).
  2. S.B.Farah, C.F.Ramos, R.K.Bortoleto, I.A.Cardinalli e P.Vogt, ``Y chromosome microdeletions in sterile males towards physical mapping of human spermatogenesis gene'', 11 Congresso latinoamercano de genetica, Mexico, 121, (1994).
  3. S.B.Farah, A.Edelmann, C.F.Ramos, O.Henegariu, P.Hirschmann, R.K.Bortoleto, R.A.Pfeiffer, I.A. Cardinallia, P.Kiesewetter e P.Vogt, ``Molecular deletions mapping of the Y chromosome in males with idiopathic azoospermia reveals a new class of microdeletions located in middle of Yq11'', 44th Annual meeting of the american society of human genetics, Canada, 55, 103, (1994).
  4. A.M.L.de A.Spin, ``Mitochondrial DNA variation in populations of the screwworm fly, Cochliomyia hominivorax (Diptera:Calliphoridae) from Brazil'', International Congress of Systematic and Evolutionary Biology, Estados Unidos, 55, (1994).
  5. L.M.Prioli, M.E.Williams e C.S.Levings III, ``Methomyl-resistant mutants of the T-urf13 gene in the Texas cytoplasm of maize'', 4th International Congress of Plant Molecular Biology, Holanda, 142, (1994).
  6. P.Vogt, A.Edelmann, P.Hirshmann, S.B.Farah, M.Hartmann, O.Haidl, P.Kiesewetter, D.Meschede, E.Nieschlag, W.Schill e W.Weidner, ``The clinical phenotype of sterile men with 46XY karyotytpe and different samll interstitial deletion in Yq11 is different'', Annual Meeting of the german human genetic society, Alemanha, 45, (1994).
  7. M.P.Mello, M.Araujo, V.P.Forrer, M.R.Sanches, L.A.Suzuki, G.Guerra Jr e S.B.Farah, ``Arranjos moleculares no complexo genico da enzima 21-hidroxilase (21-OH) em familias brasileiras'', XI concresso latino americano de genetica, Mexico, (1994).
  8. G.Guerra Jr, M.P.Mello, S.B.Farah, M.Araujo, M.T.Baptista e S.H.V.L.Marini, ``Clinical and molecular studies of 21 brazilian families with classical congenital adrenal hyperplasia due to 21-hydroxylase deficiency'', VIII Reunion Soc. Lat. de Endocrinologia Pedriatica, Chile, (1994).
  9. A.M.L.de A.Spin e M.E.Infante, ``Genetic variation and geografic differentiation in mitochondrial DNA of the primary screwworm fly, Cochliomyia hominivorax'', Annual meeting of the Entomological Soc. of America, Estados Unidos, 204, (1994).