Results : 1-25/119
Authors:
N. Risch
Journal: American journal of human genetics
Citation: N. Risch, Assessing the Role of HLA-linked and Unlinked Determinants of Disease, American journal of human genetics , 40(1), 1987, pp. 1-14
Authors:
Cannizzaro, L.A.
Croce, C.M.
Griffin, C.A.
Simeone, A.
Boncinelli, E.
Huebner, K.
Journal: American journal of human genetics
Citation: Cannizzaro, L.a et al., Human homeo box-containing genes located at chromosome regions 2q31-2q37 and 12q12-12q13, American journal of human genetics , 41-I(1), 1987, pp. 1-15
Authors:
Fabbro, D.
Desnick, R.J.
Grabowski, G.A.
Journal: American journal of human genetics
Citation: D. Fabbro, et al., Gaucher Disease: Genetic heterogeneity within and among the subtypes detected by immunoblotting, American journal of human genetics , 40(1), 1987, pp. 15-31
Authors:
Cantor, R.M.
Roy, C.
Lim, J.S.T.
Kaback, M.M.
Journal: American journal of human genetics
Citation: Cantor, R.m et al., Sandhoff disease heterozygote detection: a component of population screening for tay-sachs disease carriers. II. Sandhoff disease gene frequencies in american jewish and non-jewish populations, American journal of human genetics , 41-I(1), 1987, pp. 16-26
Authors:
Bowcock, A.M.
Farrer, L.A.
Cavalli-Sforza, L.L.
Hebert, J.M.
Kidd, K.K.
Frydman, M.
Bonne-Tamir, B.
Journal: American journal of human genetics
Citation: Bowcock, A.m et al., Mapping the wilson disease locus to a cluster of linked polymorphic markers on chromosome 13, American journal of human genetics , 41-I(1), 1987, pp. 27-35
Authors:
Ferraris, A.M.
Melani, C.
Canepa, L.
Meloni, T.
Forteleoni, G.
Gaetani, G.
Journal: American journal of human genetics
Citation: Ferraris, A.m et al., A case of ataxia telangiectasia with unbalanced glucose-6-phosphate dehydrogenase mosaicism in the granulocytic/monocytic lineages, American journal of human genetics , 40(1), 1987, pp. 32-38
Authors:
Wyatt, R.J.
Rivas, M.L.
Julian, B.A.
Quiggins, P.A.
Woodford, S.Y.
McMorrow, R.G.
Baehler, R.W.
Journal: American journal of human genetics
Citation: Wyatt, R.j et al., Regolarization in hereditary IgA nephropathy, American journal of human genetics , 41-I(1), 1987, pp. 36-50
Authors:
Gahl, W.A.
Finkelstein, J.D.
Mullen, K.D.
Bernardini, I.
Martin, J.J.
Backlund, P.
Ishak,K.G.
Hoofnagle, J.H.
Mudd, S.H.
Journal: American journal of human genetics
Citation: Gahl, W.a et al., Hepatic methionine adenosyltransferase deficiency in a 31-year-old man, American journal of human genetics , 40(1), 1987, pp. 39-49
Authors:
Robinson, B.H.
Oei, J.
Saudubray, J.M.
Marsac, C.
Bartelett, K.
Quan, F.
Gravel, R.
Journal: American journal of human genetics
Citation: Robinson, B.h et al., The french and north american phenotypes of pyruvate carboxylase deficiency correlation with biotin containing protein by H-Biotin incorporation, S-streptavidin labeling and northern blotting with a cloned cdna probe, American journal of human genetics , 40(1), 1987, pp. 50-59
Authors:
Meyers, D.A.
Beaty, T.H.
Freidhoff, L.R.
Marsh, D.G.
Journal: American journal of human genetics
Citation: Meyers, D.a et al., Inheritance of total serum IgE (Basal levels) in man, American journal of human genetics , 41-I(1), 1987, pp. 51-62
Authors:
Parry, D.M.
Berg, K.
Mulvihill, J.J.
Carter, C.L.
Miller, R.W.
Journal: American journal of human genetics
Citation: Parry, D.m et al., Strategies for controlling cancer through genetics: report of a workshop, American journal of human genetics , 41-I(1), 1987, pp. 63-69
Authors:
Hook, E.B.
Cross, P.K.
Journal: American journal of human genetics
Citation: Hook, E.b et Cross, P.k, Extra structurally abnormal chromosomes (ESAC) detected at amniocentesis: frequency in approximately 75,000 prenatal cytogenetic diagnoses and associations with maternal and paternal age, American journal of human genetics , 40(2), 1987, pp. 83-101
Authors:
Simon, M.
Le Mignon, L.
Fauchet, R.
Yaouanq, J.
David, V.
Edan, G.
Bourel, M.
Journal: American journal of human genetics
Citation: M. Simon, et al., A study of 609 HLA haplotypes marking for the hemochromatosis gene: (1) mapping of the gene near the hla-a locus and characters required to define a heterozygous population and (2) hypothesis concerning the undelying cause of hemochromatosis-hla association, American journal of human genetics , 41-I(2), 1987, pp. 89-105
Authors:
Munroe, D.G.
Chang, P.L.
Journal: American journal of human genetics
Citation: Munroe, D.g et Chang, P.l, Tissue-specific expression of human arylsulfatase-c isozymes and steroid sulfatase, American journal of human genetics , 40(2), 1987, pp. 102-114
Authors:
Stocks, J.
Paul, H.
Galton, D.
Journal: American journal of human genetics
Citation: J. Stocks, et al., Haplotypes identified by DNA restriction-fragment-lenght polymorphisms in the A-1 C-III A-IV gene region and hypertriglyceridemia, American journal of human genetics , 41-I(2), 1987, pp. 106-118
Authors:
Nigro, J.M.
Schweinfest, C.W.
Rajkovic, A.
Pavlovic, J.
Jamal, S.
Dottin, R.P.
Journal: American journal of human genetics
Citation: Nigro, J.m et al., cDNA cloning and mapping of the human creatine kinase m gene to 19q13, American journal of human genetics , 40(2), 1987, pp. 115-125
Authors:
Kamboh, M.I.
Ferrell, R.E.
Journal: American journal of human genetics
Citation: Kamboh, M.i et Ferrell, R.e, Genetic studies of human apolipoproteins. I. Polymorphism of apolipoprotein A-IV, American journal of human genetics , 41-I(2), 1987, pp. 119-127
Authors:
Saha, N.
Bhattacharyya, S.P.
Yeoh, S.C.
Chua, S.P.K.
Ratnam, S.S.
Journal: American journal of human genetics
Citation: N. Saha, et al., Glucose dehydrogenase polymorphism among ethnic groups of singapore - with report of two additional alleles, American journal of human genetics , 40(2), 1987, pp. 126-130
Authors:
Greenberg, C.R.
Hamerton, J.L.
Nigli, M.
Wrogemann, K.
Journal: American journal of human genetics
Citation: Greenberg, C.r et al., DNA studies in a family with duchenne muscular dystrophy and a deletion at Xp21, American journal of human genetics , 41-I(2), 1987, pp. 128-137
Analysis of fetal intestinal enzymes in amniotic fluid for the prenatal diagnosis of cystic fibrosis
Authors:
Mulivor, R.A.
Cook, D.
Muller, F.
Boué, A.
Gilbert, F.
Journal: American journal of human genetics
Citation: Mulivor, R.a et al., Analysis of fetal intestinal enzymes in amniotic fluid for the prenatal diagnosis of cystic fibrosis, American journal of human genetics , 40(2), 1987, pp. 131-146
Authors:
Lanman, J.T.
Bartlett, R.J.
Chen, J.C.
Yamaoka, L.
Koh, J.
Speer, M.C.
Hung, W.-Y.
Roses, A.D.
Journal: American journal of human genetics
Citation: Lanman, J.t et al., Familial inheritance of a DXS164 deletion mutation from a heterozygous female, American journal of human genetics , 41-I(2), 1987, pp. 138-144
Authors:
Bernstein, R.
Rosendorff, J.
Ramsay, M.
Pinto, M.R.
Page, D.C.
Journal: American journal of human genetics
Citation: R. Bernstein, et al., A unique dicentric X;Y translocation with Xq and Yp breakpoints: cytogenetic and molecular studies, American journal of human genetics , 41-I(2), 1987, pp. 145-156
Authors:
Carothers, A.D.
Journal: American journal of human genetics
Citation: Carothers, A.d, Down syndrome and maternal age: the effect of erroneous assignment of parental origin, American journal of human genetics , 40(2), 1987, pp. 147-150
Authors:
Holmquist, G.P.
Journal: American journal of human genetics
Citation: Holmquist, G.p, Role of replication time in the control of tissue-specific gene expression, American journal of human genetics , 40(2), 1987, pp. 151-173
Authors:
Gemmill, R.M.
Pearce-Birge, L.
Bixenman, H.
Hecht, B.K.
Allanson, J.E.
Journal: American journal of human genetics
Citation: Gemmill, R.m et al., Y chromosome-specific DNA sequences in turner-syndrome mosaicism, American journal of human genetics , 41-I(2), 1987, pp. 157-167