Results : 101-125/195
Authors:
Gessler, M.
Thomas, G. H.
Couillin, P.
Junien, C.
McGillivray, B. C.
Hayden, M.
Jaschek, G.
Bruns, G. A. P.
Journal: American journal of human genetics
Citation: M. Gessler, et al., A deletion map of the WAGR region on chromosome II, American journal of human genetics , 44(4), 1989, pp. 486-495
Authors:
Sebastio, G.
Villa, M.
Sartorio, R.
Guzzetta, V.
Poggi, V.
Auricchio, S.
Boll, W.
Mantei, N.
Semenza, G.
Journal: American journal of human genetics
Citation: G. Sebastio, et al., Control of lactase in human adult-type hypolactasia and in weaning rabbits and rats, American journal of human genetics , 45-I(4), 1989, pp. 489-497
Authors:
Lindlöf, Mikael
Anne Kiuru,
Kääriäinen, Helena
Kalimo, Hannu
Lang, Heikki
Pihko, Helena
Rapola, Juhani
Somer, Hannu
Somer, Mirja
Savontaus, Marja-Lisa
de la Chapelle, Albert
Journal: American journal of human genetics
Citation: Lindlöf, Mikael et al., Gene deletions in X-linked muscular dystrophy, American journal of human genetics , 44(4), 1989, pp. 496-503
Authors:
Koenig, M.
Beggs, A. H.
Moyer, M.
Scherpf, S.
Heinrich, K.
Bettecken, T.
Meng, G.
Muller, C. R.
Lindlof, M.
Kaariainen, H.
de la Chapelle, A.
Kiuru, A.
Savontaus, M.-L.
Gilgenkrantz, H.
Recan, D.
Chelly, J.
Kaplan, J.-C.
Covone, A. E
Archidiacono, N.
Romeo, G.
Liechti-Gallati, S.
Schneider, V.
Braga, S.
Moser, H.
Darras, B. T.
Murphy, P.
Francke, U.
Chen, J. D.
Morgan, G.
Denton, M.
Greenberg, C. R.
Wrogemann, K.
Blonden, L. A. J.
van Paassen, H. M. B.
van Ommen, G. J. B.
Kunkel, L. M.
Journal: American journal of human genetics
Citation: M. Koenig, et al., The molecular basis for duchenne versus becker muscular dystrophy: correlation of severity with type of deletion, American journal of human genetics , 45-I(4), 1989, pp. 498-506
Authors:
Hertzberg, M.
Mickleson, K. N. P.
Serjeantson, S. W.
Prior, J. F.
Trent, R. J.
Journal: American journal of human genetics
Citation: M. Hertzberg, et al., An asian-specific 9-bp deletion of mitochondrial dna is frequently found in polynesians, American journal of human genetics , 44(4), 1989, pp. 504-510
Authors:
Gillard, E. F.
Chamberlain, J. S.
Murphy, E. G.
Duff, C L.
Smith, B.
Burghes, A. H. M.
Thompson, M. W.
Sutherland, J.
Oss, I.
Bodrug, S. E.
Klamut, H. J.
Ray, P. N.
Worton, R. G.
Journal: American journal of human genetics
Citation: F. Gillard, E. et al., Molecular and phenotypic analysis of patients with deletions within the deletion-rich region of the duchenne muscular dystropay (DMD) gene, American journal of human genetics , 45-I(4), 1989, pp. 507-520
Authors:
Lyonnet, Stanislas
Caillaud, Catherine
Rey, Françoise
Berthelon, Monique
Frézal, Jean
Rey, Jean
Munnich, Arnold
Journal: American journal of human genetics
Citation: Lyonnet, Stanislas et al., Molecular genetics of phenylketonuria in mediterranean countries: a mutation associated with partial phenylalanine hydroxylase deficiency, American journal of human genetics , 44(4), 1989, pp. 511-517
Authors:
Chamberlain, Susan
Shaw, Jacqui
Wallis, Julie
Rowland, Alison
Chow, Larry
Farrall, Martin
Keats, Bronya
Richter, Andrea
Roy, Madeleine
Melancon, Serge
Deufel, Thomas
Berciano, José
Williamson, Robert
Journal: American journal of human genetics
Citation: Chamberlain, Susan et al., Genetic homogeneity at the friedreich ataxia locus on chromosome 9, American journal of human genetics , 44(4), 1989, pp. 518-521
Authors:
Schildkraut, Joellen M.
Risch, Neil
Thompson, W. Douglas
Journal: American journal of human genetics
Citation: M. Schildkraut, Joellen et al., Evaluating genetic association among ovarian, breast, and endometrial cancer: evidence for a breast-ovarian cancer relationship, American journal of human genetics , 45-I(4), 1989, pp. 521-529
Authors:
Lobos, Elizabeth A.
Rudnick, Caroline H.
Watson, Michael S.
Isenberg, Keith E.
Journal: American journal of human genetics
Citation: A. Lobos, Elizabeth et al., Linkage disequilibrium study of RFLPs detected at the human muscle nicotinic acetylcholine receptor subunit genes, American journal of human genetics , 44(4), 1989, pp. 522-533
Authors:
Merry, Diane E.
Lesko, John G.
Sosnoski, Donna M.
Lewis, Richard A.
Lubinsky, Mark
Trask, Barbara
van den Engh, Ger
Collins, Francis S.
Nussbaum, Robert L.
Journal: American journal of human genetics
Citation: E. Merry, Diane et al., Choroideremia and deafness with stapes fixation: a contiguous gene deletion syndrome in Xq21, American journal of human genetics , 45-I(4), 1989, pp. 530-540
Authors:
Baker, Rohan T.
Board, Philip G.
Journal: American journal of human genetics
Citation: T. Baker, Rohan et G. Board, Philip, Unequal crossover generates variation in ubiquitin coding unit number at the human ubc polyubiquitin locus, American journal of human genetics , 44(4), 1989, pp. 534-542
Authors:
Payami, Haydeh
Joe, Sharon
Farid, Nadir R.
Stenszky, Valeria
Chan, S. H.
Yeo, P. P. B.
Cheah, J. S.
Thomson, Glenys
Journal: American journal of human genetics
Citation: Payami, Haydeh et al., Relative predispositional effects (RPEs) of marker alleles with disease: HLA-DR alleles and graves disease, American journal of human genetics , 45-I(4), 1989, pp. 541-546
Authors:
Ploughman, Lynn M.
Boehnke, Michael
Journal: American journal of human genetics
Citation: M. Ploughman, Lynn et Boehnke, Michael, Estimating the power of a proposed linkage study for a complex genetic trait, American journal of human genetics , 44(4), 1989, pp. 543-551
Authors:
Yandell, David W.
Dryja, Thaddeus P.
Journal: American journal of human genetics
Citation: W. Yandell, David et P. Dryja, Thaddeus, Detection of DNA sequence polymorphisms by enzymatic amplification and direct genomic sequencing, American journal of human genetics , 45-I(4), 1989, pp. 547-555
Authors:
Martinez, Maria M.
Goldin, Lynn R.
Journal: American journal of human genetics
Citation: M. Martinez, Maria et R. Goldin, Lynn, The detection of linkage and heterogeneity in nuclear families for complex disorders: one versus two marker loci, American journal of human genetics , 44(4), 1989, pp. 552-559
Authors:
Maestri, Nancy E.
Beaty, Terri H.
Boughman, Joann A.
Journal: American journal of human genetics
Citation: E. Maestri, Nancy et al., Etiologic heterogeneity in the familial aggregation of congenital cardiovascular malformations, American journal of human genetics , 45-I(4), 1989, pp. 556-564
Authors:
Skraastad, M. I.
Bakker, E.
de Lange, L. F.
Vegter-van der Vlis, M.
Klein-Breteler, E. G.
van Ommen, G. J. B.
Pearson, P. L.
Journal: American journal of human genetics
Citation: I. Skraastad, M. et al., Mapping of recombinant near the huntington disease locus by using G8 (D4S10) and newly isolated markers in the D4SI0 region, American journal of human genetics , 44(4), 1989, pp. 560-566
Authors:
Misra, Brijesh C.
Srivatsan, Eri S.
Journal: American journal of human genetics
Citation: C. Misra, Brijesh et S. Srivatsan, Eri, Localization of hela cell tumor-suppressor gene to the long arm of chromosome II, American journal of human genetics , 45-I(4), 1989, pp. 565-577
Authors:
Chen, Shi-Han
Scott, C. Ronald
Schoof, Jonathan
Lovrien, Everett W.
Kurachi, Kotoku
Journal: American journal of human genetics
Citation: Chen, Shi-han et al., Factor ixportland: a nonsense mutation (GA to IGA) resulting in hemophilia B, American journal of human genetics , 44(4), 1989, pp. 567-569
Authors:
Bradley, Daniel G.
Farrar, G. Jane
Sharp, Elizabeth M.
Kenna, Paul
Humphries, Marian M.
McConnell, David J.
Daiger, Stephen P.
McWilliam, Peter
Humphries, Peter
Journal: American journal of human genetics
Citation: G. Bradley, Daniel et al., Autosomal dominant retinitis pigmentosa: exclusion of the gene from the short arm of chromosome i including the region surrounding the rhesus locus, American journal of human genetics , 44(4), 1989, pp. 570-576
Authors:
Hall, Jeffrey M.
Zuppan, Patricia J.
Anderson, Lee A.
Huey, Bing
Carter, Christine
King, Mary-Claire
Journal: American journal of human genetics
Citation: M. Hall, Jeffrey et al., Oncogenes and human breast cancer, American journal of human genetics , 44(4), 1989, pp. 577-584
Authors:
Gershon, Elliot S.
Martinez, Maria
Goldin, Lynn
Gelernter, Joel
Silver, Jonathan
Journal: American journal of human genetics
Citation: S. Gershon, Elliot et al., Detection of marker associations with a dominant disease gene in genetically complex and heterogeneous diseases, American journal of human genetics , 45-I(4), 1989, pp. 578-585
Authors:
Sepehrnia, B.
Kamboh, M. I.
Adams-Campbell, L. L.
Bunker, C. H.
Nwankwo, M.
Majumder, P. P.
Ferrell, R. E.
Journal: American journal of human genetics
Citation: B. Sepehrnia, et al., Genetic studies of human apolipoproteins. X. the effect of the apoliproprotein e polymorphism on quantitative levels of lipoproteins in nigerian blacks, American journal of human genetics , 45-I(4), 1989, pp. 586-591
Authors:
Brown, Carolyn J.
Willard, Huntington F.
Journal: American journal of human genetics
Citation: J. Brown, Carolyn et F. Willard, Huntington, Noninactivation of a selectable human X-linked gene that complements a murine temperature-sensitive cell cycle defect, American journal of human genetics , 45-I(4), 1989, pp. 592-598