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  1. 1
    Whole Exome Sequencing Reveals Mutations in Known Retinal Disease Genes in 33 out of 68 Israeli Families with Inherited Retinopathies

    Whole Exome Sequencing Reveals Mutations in Known Retinal Disease Genes in 33 out of 68 Israeli Families with Inherited Retinopathies mā Avigail Beryozkin, Elia Shevah, Adva Kimchi, Liliana Mizrahi‐Meissonnier, Samer Khateb, Rinki Ratnapriya, Csilla H. Lazar, Anat Blumenfeld, Tamar Ben‐Yosef, Yitzhak Hemo, Jacob Pe’er, Eduard Averbuch, Michal Sagi, Alexis Boleda, Linn Gieser, Abraham Zlotogorski, Tzipora C. Falik‐Zaccai, Ola Alimi-Kasem, Samuel G. Jacobson, Itay Chowers, Anand Swaroop, Eyal Banin, Dror Sharon

    I whakaputaina 2015
    Whiwhi kuputuhi katoa Whiwhi kuputuhi katoa
    Artigo
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  2. 2
    The Two Common Mutations Causing Factor XI Deficiency in Jews Stem From Distinct Founders: One of Ancient Middle Eastern Origin and Another of More Recent European Origin

    The Two Common Mutations Causing Factor XI Deficiency in Jews Stem From Distinct Founders: One of Ancient Middle Eastern Origin and Another of More Recent European Origin mā Hava Peretz, Avital Mulai, Sali Usher, Ariella Zivelin, Avihai Segal, Zahavi Weisman, Moshe Mittelman, Hannah Lupo, Naomi Lanir, Benjamin Brenner, Ofer Shpilberg, Uri Seligsohn

    I whakaputaina 1997
    Whiwhi kuputuhi katoa Whiwhi kuputuhi katoa
    Artigo
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  3. 3
    Prevalence of <i>BRCA1</i> and <i>BRCA2</i> mutations in Ashkenazi Jewish families with breast and pancreatic cancer

    Prevalence of <i>BRCA1</i> and <i>BRCA2</i> mutations in Ashkenazi Jewish families with breast and pancreatic cancer mā Zsofia K. Stadler, Erin Salo‐Mullen, Sujata M. Patil, M. Catherine Pietanza, Joseph Vijai, Emmanouil Saloustros, Nichole Hansen, Noah D. Kauff, Robert C. Kurtz, David P. Kelsen, Kenneth Offit, Mark E. Robson

    I whakaputaina 2011
    Whiwhi kuputuhi katoa Whiwhi kuputuhi katoa
    Artigo
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  4. 4
    High carrier frequency of the 35delG deafness mutation in European populations

    High carrier frequency of the 35delG deafness mutation in European populations mā Paolo Gasparini, Raquel Rabionet, Guido Barbujani, Salvatore Melchionda, M B Petersen, Karen Brøndum‐Nielsen, Andres Metspalu, Eneli Oitmaa, Marina Pisano, Paolo Fortina, L. Zelante, Xavier Estivill

    I whakaputaina 2000
    Whiwhi kuputuhi katoa Whiwhi kuputuhi katoa
    Artigo
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  5. 5
    The spectrum of genetic defects in a panel of 40 Dutch families with symptomatic protein C deficiency type I: heterogeneity and founder effects

    The spectrum of genetic defects in a panel of 40 Dutch families with symptomatic protein C deficiency type I: heterogeneity and founder effects mā PH Reitsma, SR Poort, C.F. Allaart, E Briët, R M Bertina

    I whakaputaina 1991
    Whiwhi kuputuhi katoa Whiwhi kuputuhi katoa
    Artigo
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  6. 6
    Carrier frequency of the IVS4 + 4 A--&gt;T mutation of the Fanconi anemia gene FAC in the Ashkenazi Jewish population

    Carrier frequency of the IVS4 + 4 A--&gt;T mutation of the Fanconi anemia gene FAC in the Ashkenazi Jewish population mā PC Verlander, A.G. Kaporis, Q. Liu, Qingjiong Zhang, Uri Seligsohn, AD Auerbach

    I whakaputaina 1995
    Whiwhi kuputuhi katoa Whiwhi kuputuhi katoa
    Artigo
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  7. 7
    Bottlenecks in HIV-1 transmission: insights from the study of founder viruses

    Bottlenecks in HIV-1 transmission: insights from the study of founder viruses mā Sarah Joseph, Ronald Swanstrom, Angela D. M. Kashuba, Myron S. Cohen

    I whakaputaina 2015
    Whiwhi kuputuhi katoa
    Revisão
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  8. 8
    ‘Ghost’ alleles of the Mauritius kestrel

    ‘Ghost’ alleles of the Mauritius kestrel mā J. J. Groombridge, Carl G. Jones, Michael W. Bruford, Richard A. Nichols

    I whakaputaina 2000
    Whiwhi kuputuhi katoa Whiwhi kuputuhi katoa
    Artigo
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  9. 9
    Interpretation of patterns of genetic variation in endemic plant species of oceanic islands

    Interpretation of patterns of genetic variation in endemic plant species of oceanic islands mā Tod F. Stuessy, Kōji Takayama, Patricio López‐Sepúlveda, Daniel J. Crawford

    I whakaputaina 2013
    Whiwhi kuputuhi katoa Whiwhi kuputuhi katoa
    Revisão
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  10. 10
    A high proportion of novel mutations in BRCA1 with strong founder effects among Dutch and Belgian hereditary breast and ovarian cancer families.

    A high proportion of novel mutations in BRCA1 with strong founder effects among Dutch and Belgian hereditary breast and ovarian cancer families. mā Tamara Peelen, M van Vliet, Anne Petrij-Bosch, R Mieremet, Csilla I. Szabo, Ans MW van den Ouweland, Frans B.L. Hogervorst, Richard M. Brohet, M.J.L. Ligtenberg, Erik Teugels, Rob B. van der Luijt, Annemarie H. van der Hout, Gilles Thomas, Gerard Pals, Inge Jedema, Renske Olmer, Ingeborg van Leeuwen, Beth Newman, M Plandsoen, Mieke van der Est, Gijs R. van den Brink, S. Hageman, P J Arts, Egbert Bakker, Peter Devilee

    I whakaputaina 1997
    Whiwhi kuputuhi katoa
    Artigo
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  11. 11
    Population history and its impact on medical genetics in Quebec

    Population history and its impact on medical genetics in Quebec mā A‐M Laberge, Jacques L. Michaud, Andréa Richter, Emmanuelle Lemyre, M Lambert, Bernard Brais, GA Mitchell

    I whakaputaina 2005
    Whiwhi kuputuhi katoa Whiwhi kuputuhi katoa
    Revisão
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  12. 12
    Genomic diversity and differentiation of a managed island wild boar population

    Genomic diversity and differentiation of a managed island wild boar population mā Laura Iacolina, Massimo Scandura, Daniël J. Goedbloed, Panoraia Alexandri, R.P.M.A. Crooijmans, Greger Larson, Alan Archibald, Marco Apollonio, Lawrence B. Schook, Martien A. M. Groenen, Hendrik‐Jan Megens

    I whakaputaina 2015
    Whiwhi kuputuhi katoa Whiwhi kuputuhi katoa
    Artigo
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  13. 13
    Height-reducing variants and selection for short stature in Sardinia

    Height-reducing variants and selection for short stature in Sardinia mā Magdalena Żołędziewska, Carlo Sidore, Charleston W. K. Chiang, Serena Sanna, Antonella Mulas, Maristella Steri, Fabio Busonero, Joseph Marcus, Michele Marongiu, Andrea Maschio, Diego Ortega‐Del Vecchyo, Matteo Floris, Antonella Meloni, Alessandro Delitala, Maria Pina Concas, Federico Murgia, Ginevra Biino, Simona Vaccargiu, Ramaiah Nagaraja, Kirk E. Lohmueller, Nicholas J. Timpson, Nicole Soranzo, Ioanna Tachmazidou, George Dedoussis, Eleftheria Zeggini, Sergio Uzzau, Chris Jones, Robert Lyons, Andrea Angius, Gonçalo R. Abecasis, John Novembre, David Schlessinger, Francesco Cucca

    I whakaputaina 2015
    Whiwhi kuputuhi katoa
    Artigo
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  14. 14
    A common founder for the 35delG GJB2 gene mutation in connexin 26 hearing impairment

    A common founder for the 35delG GJB2 gene mutation in connexin 26 hearing impairment mā L. Van Laer

    I whakaputaina 2001
    Whiwhi kuputuhi katoa Whiwhi kuputuhi katoa
    Artigo
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  15. 15
    DETECTING RANGE EXPANSIONS FROM GENETIC DATA

    DETECTING RANGE EXPANSIONS FROM GENETIC DATA mā Benjamin M. Peter, Montgomery Slatkin

    I whakaputaina 2013
    Whiwhi kuputuhi katoa
    Artigo
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  16. 16
    Identification of a single ancestral CYP1B1 mutation in Slovak Gypsies (Roms) affected with primary congenital glaucoma

    Identification of a single ancestral CYP1B1 mutation in Slovak Gypsies (Roms) affected with primary congenital glaucoma mā Martina Plášilová, Ivaylo Stoilov, Mansoor Sarfarazi, L Kádasi, Eva Feráková, V. Ferák

    I whakaputaina 1999
    Whiwhi kuputuhi katoa Whiwhi kuputuhi katoa
    Artigo
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  17. 17
    Mitochondrial DNA Variation of Modern Tuscans Supports the Near Eastern Origin of Etruscans

    Mitochondrial DNA Variation of Modern Tuscans Supports the Near Eastern Origin of Etruscans mā Alessandro Achilli, Anna Olivieri, Maria Pala, Ene Metspalu, Simona Fornarino, Vincenza Battaglia, Matteo Accetturo, Ildus Kutuev, Э. К. Хуснутдинова, Erwan Pennarun, N. Cerutti, Cornelia Di Gaetano, Francesca Crobu, Domenico Palli, Giuseppe Matullo, A. Silvana Santachiara‐Benerecetti, Luigi Luca Cavalli-Sforza, Ornella Semino, Richard Villems, Hans-Jürgen Bandelt, Alberto Piazza, Antonio Torroni

    I whakaputaina 2007
    Whiwhi kuputuhi katoa Whiwhi kuputuhi katoa
    Artigo
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  18. 18
    Reconstructing Roma History from Genome-Wide Data

    Reconstructing Roma History from Genome-Wide Data mā Priya Moorjani, Nick Patterson, Po‐Ru Loh, Mark Lipson, Péter Kisfali, Béla Melegh, Michael Bonin, Ľudevít Kádaši, Olaf Rieß, Bonnie Berger, David Reich, Béla Melegh

    I whakaputaina 2013
    Whiwhi kuputuhi katoa Whiwhi kuputuhi katoa
    Artigo
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  19. 19
    Signatures of founder effects, admixture, and selection in the Ashkenazi Jewish population

    Signatures of founder effects, admixture, and selection in the Ashkenazi Jewish population mā Steven M. Bray, Jennifer G. Mullé, Anne Dodd, Ann E. Pulver, Stephen Wooding, Stephen T. Warren

    I whakaputaina 2010
    Whiwhi kuputuhi katoa
    Artigo
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  20. 20
    The exon 55 deletion in the nebulin gene – One single founder mutation with world-wide occurrence

    The exon 55 deletion in the nebulin gene – One single founder mutation with world-wide occurrence mā Vilma‐Lotta Lehtokari, Rebecca S. Greenleaf, Elizabeth T. DeChene, Mutsumi Kellinsalmi, Katarina Pelin, Nigel G. Laing, Alan H. Beggs, Carina Wallgren‐Pettersson

    I whakaputaina 2009
    Whiwhi kuputuhi katoa
    Artigo
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