Sökresultat - Bharti Morar

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  1. 1
    KIBRA genetic polymorphism influences episodic memory in later life, but does not increase the risk of mild cognitive impairment

    KIBRA genetic polymorphism influences episodic memory in later life, but does not increase the risk of mild cognitive impairment av Osvaldo P. Almeida, S.G. Schwab, Nicola T. Lautenschlager, Bharti Morar, Kathryn R. Greenop, Leon Flicker, Dieter B. Wildenauer

    Publicerad 2008
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  2. 2
    Deleterious GRM1 Mutations in Schizophrenia

    Deleterious GRM1 Mutations in Schizophrenia av Mohammed Akli Ayoub, Dora Angelicheva, David Vile, David Chandler, Bharti Morar, Juleen A. Cavanaugh, Peter M. Visscher, Assen Jablensky, Kevin D. G. Pfleger, Luba Kalaydjieva

    Publicerad 2012
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  3. 3
    Transcriptome-wide effects of a<i>POLR3A</i>gene mutation in patients with an unusual phenotype of striatal involvement

    Transcriptome-wide effects of a<i>POLR3A</i>gene mutation in patients with an unusual phenotype of striatal involvement av Dimitar N. Azmanov, Stefan J. Siira, Teodora Chamova, Ara Kaprelyan, Velina Guergueltcheva, Anne-Marie J. Shearwood, Ganqiang Liu, Bharti Morar, Oliver Rackham, Michael Bynevelt, Маргарита Грудкова, Zdravko Kamenov, Vassil Svechtarov, Ivailo Tournev, Luba Kalaydjieva, Aleksandra Filipovska

    Publicerad 2016
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  4. 4
    Origins and Divergence of the Roma (Gypsies)

    Origins and Divergence of the Roma (Gypsies) av David Gresham, Bharti Morar, Peter A. Underhill, Giuseppe Passarino, Alice A. Lin, C. Wise, Dora Angelicheva, Francesc Calafell, Peter J. Oefner, Peidong Shen, Ivailo Tournev, Rosario de Pablo, V. Kučinskas, Anna Pérez-Lezaun, Elena Marushiaková, Vesselin Popov, Luba Kalaydjieva

    Publicerad 2001
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  5. 5
    Autosomal-Recessive Congenital Cerebellar Ataxia Is Caused by Mutations in Metabotropic Glutamate Receptor 1

    Autosomal-Recessive Congenital Cerebellar Ataxia Is Caused by Mutations in Metabotropic Glutamate Receptor 1 av Velina Guergueltcheva, Dimitar N. Azmanov, Dora Angelicheva, Katherine R. Smith, Teodora Chamova, Laura V. Flórez, Michael Bynevelt, Thai B. Nguyen, Sylvia Cherninkova, Veneta Bojinova, Ara Kaprelyan, Lyudmila Angelova, Bharti Morar, David Chandler, Radka Kaneva, Melanie Bahlo, Ivailo Tournev, Luba Kalaydjieva

    Publicerad 2012
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  6. 6
    The Effective Mutation Rate at Y Chromosome Short Tandem Repeats, with Application to Human Population-Divergence Time

    The Effective Mutation Rate at Y Chromosome Short Tandem Repeats, with Application to Human Population-Divergence Time av Lev A. Zhivotovsky, Peter A. Underhill, Cengiz Cinnioğlu, Manfred Kayser, Bharti Morar, Toomas Kivisild, Rosaria Scozzari, Fulvio Cruciani, Giovanni Destro‐Bisol, Gabriella Spedini, Geoffrey K. Chambers, René J. Herrera, Kiau Kiun Yong, David Gresham, Ivailo Tournev, Marcus W. Feldman, Luba Kalaydjieva

    Publicerad 2004
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  7. 7
    Integrin Alpha 8 Recessive Mutations Are Responsible for Bilateral Renal Agenesis in Humans

    Integrin Alpha 8 Recessive Mutations Are Responsible for Bilateral Renal Agenesis in Humans av Camille Humbert, Flora Silbermann, Bharti Morar, Mélanie Parisot, Mohammed Zarhrate, Cécile Masson, Frédéric Torès, Patricia Blanchet, Marie-José Perez, Yuliya Petrov, Philippe Khau Van Kien, J. Roume, Brigitte Leroy, Olivier Gribouval, Luba Kalaydjieva, Laurence Heidet, Rémi Salomon, Corinne Antignac, Alexandre Benmerah, Sophie Saunier, Marc Jeanpierre

    Publicerad 2014
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  8. 8
    Mutation History of the Roma/Gypsies

    Mutation History of the Roma/Gypsies av Bharti Morar, David Gresham, Dora Angelicheva, Ivailo Tournev, Rebecca Gooding, Velina Guergueltcheva, Carolin Schmidt, Angela Abicht, Hanns Lochmüller, Attila Tordai, Lajos Kalmár, Melinda Nagy, Veronika Karcagi, Marc Jeanpierre, Ágnes Herczegfalvi, David Beeson, Viswanathan Venkataraman, Kim Warwick Carter, J. Reeve, Rosario de Pablo, Vaidutis Kučinskas, Luba Kalaydjieva

    Publicerad 2004
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  9. 9
    LTBP2 and CYP1B1 mutations and associated ocular phenotypes in the Roma/Gypsy founder population

    LTBP2 and CYP1B1 mutations and associated ocular phenotypes in the Roma/Gypsy founder population av Dimitar N. Azmanov, С. Димитрова, Laura V. Flórez, Sylvia Cherninkova, Dragomir Draganov, Bharti Morar, Rosmawati Saat, Manel Juan, Juan I. Aróstegui, Sriparna Ganguly, Himla Soodyall, Subhabrata Chakrabarti, Harish Padh, Miguel Ángel López‐Nevot, Violeta Chernodrinska, Botio Anguelov, Partha P. Majumder, Lyudmila Angelova, Radka Kaneva, David A. Mackey, Ivailo Tournev, Luba Kalaydjieva

    Publicerad 2010
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  10. 10
    <i>UFM1</i> founder mutation in the Roma population causes recessive variant of H-ABC

    <i>UFM1</i> founder mutation in the Roma population causes recessive variant of H-ABC av Eline M. Hamilton, Enrico Bertini, Luba Kalaydjieva, Bharti Morar, Dana Dojčáková, Judy Liu, Adeline Vanderver, Julian Curiel, Claudia M. Persoon, Daria Diodato, Lorenzo Pinelli, Nathalie L. van der Meij, Barbara Plecko, Susan Blasér, Nicole I. Wolf, Quinten Waisfisz, Truus E. M. Abbink, Marjo S. van der Knaap, Adele D’Amico, Ana Raguž, Paola la Boria, Graziella Cefalo, Argirios Dinopoulos, Sira Domènech, Maria Alice Donati, Daniele Frattini, Serena Gasperini, Lucio Giordano, Elena Procopio, Anita Rauch, Agustí Rodríguez‐Palmero, Komudi Siriwardena, Miguel Tomás‐Vila

    Publicerad 2017
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