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Results: 1-25/11430
Authors:
Ehnholm Christian
Sistonen Pertti
Citation: Ehnholm Christian et Sistonen Pertti, On the Heritability of Serum High Density Lipoprotein in Twins, American journal of human genetics , 32(1), 1980, pp. 1-7
Authors:
Edwards, Stephen M.
Kote-Jarai, Zsofia
Meitz, Julia
Hamoudi, Rifat
Hope, Questa
Osin, Peter
Jackson, Rachel
Southgate, Christine
Singh, Rashmi
Faconer, Alison
Dearnaley, David P.
Ardern-Jones, Audrey
Murkin, Annette
Dowe, Anna
Kelly, Jo
Williams, Sue
Oram, Richard
Stevens, Margaret
Teare, Dawn M.
Ponder, A.J. Bruce
Gayther, Simon A.
Cancer Research UK/British Prostate Group UK Familial Prostate Cancer Study Coll
British Association of Urological Surgeons Section of Oncology,
Easton, Doug F.
Eeles, Rosalind A.
Citation: M. Edwards, Stephen et al., Two Percent of Men with Early-Onset Prostate Cancer Harbor Germline Mutations in the BRCA2 Gene, American journal of human genetics , 72(1), 2003, pp. 1-12
Authors:
Tang, Hua
Coram, Marc
Wang, Pei
Zhu, Xiaofeng
Risch, Neil
Citation: Tang, Hua et al., Reconstructing Genetic Ancestry Blocks in Admixed Individuals, American journal of human genetics , 79(1), 2006, pp. 1-12
Authors:
Barbouti, Aikaterini
Stankiewicz, Pawel
Nusbaum, Chad
Cuomo, Christina
Cook, April
Höglund, Mattias
Johansson, Bertil
Hagemeijer, Anne
Park, Sung-Sup
Mitelman, Felix
Lupski, James R.
Fioretos, Thoas
Citation: Barbouti, Aikaterini et al., The Breakpoint Region of the Most Common Isochromosome, i(17q), in Human Neoplasia Is Characterized by a Complex Genomic Architecture with Large, Palindromic, Low-Copy Repeats, American journal of human genetics , 74(1), 2004, pp. 1-10
Authors:
Yoshida, A.
Citation: A. Yoshida,, Biochemical Genetics of Human Blood Group ABO System, American journal of human genetics , 34(1), 1982, pp. 1-14
Authors:
Mudd, S. H. , Skovby, F. , Levy, H. L. , Pettigrew, K. D. , Wilcken, B. , Pyerit
Citation: Mudd, S. H. , Skovby, F. , Levy, H. L. , Pettigrew, K. D. , Wilcken, B. , Pyerit, The natural history of homocystinuria due to cystathionine beta-synthase deficiency, American journal of human genetics , 37(1), 1985, pp. 1-31
Authors:
Cannizzaro, L.A.
Croce, C.M.
Griffin, C.A.
Simeone, A.
Boncinelli, E.
Huebner, K.
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:
Lowden J. A.
O' Brien John S.
Citation: A. Lowden J. et S. O' Brien John, Sialidosis: A Review oh Human Neuraminidase Deficiency, American journal of human genetics , 31(1), 1979, pp. 1-18
Authors:
Slunghter, C. A.
Gogolin, K. J.
Coseo, M. C.
Meyer, L. J.
Lesko, J.
Harris, H.
Citation: A. Slunghter, C. et al., Discrimination of Human Placental Alkaline Phosphatase Allelic Variants by Monoclonal Antibodies, American journal of human genetics , 35(1), 1983, pp. 1-20
Authors:
Stoetzel, Corinne
Muller, Jean
Laurier, Virginie
Davis, Erica E.
Zaghloul, Norann A
Vicaire, Serge
Jacquelin, Cécile
Plewniak, Frédéric
Leitch, Carmen C.
Sarda, Pierre
Hamel, Christian
De Ravel, Thomy J.L.
Lewis, Richard Alan
Friederich, Evelyne
Thibault, Christelle
Danse, Jean-Marc
Verloes, Alain
Bonneau, Dominique
Katsanis, Nicholas
Poch, Olivier
Dollfus, Hélène
Citation: Stoetzel, Corinne et al., Identification of a Novel BBS Gene (BBS12) Highlights the Major Role of a Vertebrate-Specific Branch of Chaperonin-Related Proteins in Bardet-Biedl Syndrome, American journal of human genetics , 80(1), 2007, pp. 1-11
Authors:
J. Overhauser, M. S. Golbus. S. A. Schonberg, and J. J. Wasmuth
Citation: J. Overhauser, M. S. Golbus. S. A. Schonberg, And J. J. Wasmuth, Molecular Analysis of an Unbalanced Deletion of the Short Arm of Chromosome 5 That Produces No Phenotype., American journal of human genetics , 39(1), 1986, pp. 1-10
Authors:
Delague, Valérie
Jacquier, Arnaud
Hamadouche, Tarik
Poitelon, Yannick
Baudot, Cécile
Boccaccio, Irène
Chouery, Eliane
Chaouch, Malika
Kassouri, Nora
Jabbour, Rosette
Grid, Djamel
Mégarbané, André
Haase, Georg
Lévy, Nicolas
Citation: Delague, Valérie et al., Mutations in FGD4 Encoding the Rho GDP/GTP Exchange Factor FRABIN Cause Autosomal Recessive Charcot-Marie-Tooth Type 4H, American journal of human genetics , 81(1), 2007, pp. 1-16
Authors:
Barton Childs
Huether Carl A.
Murphy Edmond A.
Citation: Barton Childs et al., Human Genetics Teaching in U.S. Medical Schools, American journal of human genetics , 33(1), 1981, pp. 1-10
Authors:
Kazazian, H. H. Jr.
Citation: Kazazian, H. H. Jr, The William Allan Memorial Award Presentation, American journal of human genetics , 38(1), 1986, pp. 1-3
Authors:
N. Risch
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:
Shaw, M. W.
Citation: W. Shaw, M., To be or not to be? That is the Question, American journal of human genetics , 36(1), 1984, pp. 1-9
Authors:
Willard Huntington F.
Mellman Ira S.
Rosenberg Leon E.
Citation: F. Willard Huntington et al., Genetic Complementation among Inherited Deficies of Methymalonyl-CoA Mutase Activity: Evidence for a New Class of Human Cobalamin Mutant, American journal of human genetics , 30(1), 1978, pp. 1-13
Authors:
Trask, Barbara J.
Massa, Hillary
Kenwrick, Sue
Gitschier, Jane
Citation: J. Trask, Barbara et al., Mapping of human chromosome Xq28 by two-color fluorescence in situ hybridization of DNA sequences to interphase cell nuclei., American journal of human genetics , 48-I(1), 1991, pp. 1-15
Authors:
Gouya, Laurent
Martin-Schmitt, Caroline
Robreau, Anne-Marie
Austerlitz, Frédéric
Da Silva, Vasco
Brun, Patrick
Simonin, Sylvie
Lyoumi, Saïd
Grandchamp, Bernard
Beaumont, Carole
Puy, Hervé
Deybach, Jean-Charles
Citation: Gouya, Laurent et al., Contribution of a Common Single-Nucleotide Polymorphism to the Genetic Predisposition for Erythropoietic Protoporphyria, American journal of human genetics , 78(1), 2006, pp. 2-14
Authors:
Ikeda, Yoshio
Dalton, Joline C.
Moseley, Melinda L.
Gardner, Kathy L.
Bird, Thomas D.
Ashizawa, Tetsuo
Seltzer, William K.
Pandolfo, Massimo
Milunsky, Aubrey
Potter, Nicholas T.
Shoji, Mikio
Vincent, John B.
Day, John W.
Ranum, Laura P.W.
Citation: Ikeda, Yoshio et al., Spinocerebellar Ataxia Type 8: Molecular Genetic Comparisonsand Haplotype Analysis of 37 Families with Ataxia, American journal of human genetics , 75(1), 2004, pp. 3-16
Authors:
Ramsay, Michele
Bernstein, Renee
Zwane, Esther
Page, David C.
Jenkins, Trefor
Citation: Ramsay, Michele et al., XX true hermaphroditism in southern african blacks: an enigma of primary sexual differentiation, American journal of human genetics , 43-I(1), 1988, pp. 4-13
Authors:
Kan, Y. W.
Citation: W. Kan, Y., The William Allan Memorial Award Address: Thalassemia: Molecular Mechanism and Detection, American journal of human genetics , 38(1), 1986, pp. 4-12
Authors:
Huggings, Marlene
Bloch, Maurice
Kanani Shelin
Quarrell, Oliver W. J.
Theilman, Jane
Hedrik, Amy
Dickens, Bernard
lynch, Abbyan
Hayden Michael
Citation: Huggings, Marlene et al., ethical and legal dilemmas arising during predective testing for adult-onset disease: the experience of hungtington disease, American journal of human genetics , 47-I(1), 1990, pp. 4-12
Authors:
Murray, Louann W.
Bautista, Jose
James, Payton L.
Rimoin, David L.
Citation: W. Murray, Louann et al., Type II collagen defects in the chondrodysplasias. I. spondyloepiphyseal dysplasias, American journal of human genetics , 45-I(1), 1989, pp. 5-15
Authors:
Ikonen, Elina
Palo, Jorma
Ott, jurg
Gusella, James
Somer, Hannu
Karila, Leena
Palotie, Aarno
Peltonen, Leena
Citation: Ikonen, Elina et al., Huntington disease in finland: linkage disequilibrium of chromosome 4 RELP haplotypes and exclusion of a tight linkage between the disease and D4S43 locus, American journal of human genetics , 46-I(1), 1990, pp. 5-11