Search Results - Navid Almadani

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  1. 1
    Clinical data for 185 infertile Iranian men with Y-chromosome microdeletion

    Clinical data for 185 infertile Iranian men with Y-chromosome microdeletion by Mehdi Totonchi, Anahita Mohseni Meybodi, Parnaz Borjian Boroujeni, Mohammad Sedighi Gilani, Navid Almadani, Hamid Gourabi

    Published 2012
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  2. 2
    Sensorineural deafness and male infertility: a contiguous gene deletion syndrome

    Sensorineural deafness and male infertility: a contiguous gene deletion syndrome by Y. Zhang, Mahdi Malekpour, Navid Almadani, Kimia Kahrizi, M. Zanganeh, Marzieh Mohseni, Faezeh Mojahedi, Ahmad Daneshi, Hossein Najmabadi, Richard J. Smith

    Published 2006
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  3. 3
    Screening for <i>MYO15A</i> gene mutations in autosomal recessive nonsyndromic, <i>GJB2</i> negative Iranian deaf population

    Screening for <i>MYO15A</i> gene mutations in autosomal recessive nonsyndromic, <i>GJB2</i> negative Iranian deaf population by Zohreh Fattahi, A. Eliot Shearer, Mojgan Babanejad, Niloofar Bazazzadegan, Seyed Navid Almadani, Nooshin Nikzat, Khadijeh Jalalvand, Sanaz Arzhangi, Fatemehsadat Esteghamat, Rezvan Abtahi, Batool Azadeh, Richard J. Smith, Kimia Kahrizi, Hossein Najmabadi

    Published 2012
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  4. 4
    Whole-exome sequencing of familial cases of multiple morphological abnormalities of the sperm flagella (MMAF) reveals new<i>DNAH1</i>mutations

    Whole-exome sequencing of familial cases of multiple morphological abnormalities of the sperm flagella (MMAF) reveals new<i>DNAH1</i>mutations by Amir Amiri‐Yekta, Charles Coutton, Zine‐Eddine Kherraf, Thomas Karaouzène, Pauline Le Tanno, Mohammad Hossein Sanati, Marjan Sabbaghian, Navid Almadani, Mohammad Ali Sadighi Gilani, Seyedeh Hanieh Hosseini, Salahadin Bahrami, Abbas Daneshipour, Maurizio Bini, Christophe Arnoult, Roberto Colombo, Hamid Gourabi, Pierre F. Ray

    Published 2016
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  5. 5
    A molecular and clinical study of Larsen syndrome caused by mutations in FLNB

    A molecular and clinical study of Larsen syndrome caused by mutations in FLNB by Louise S. Bicknell, Claire Farrington‐Rock, Yousef Shafeghati, Patrick Rump, Yasemin Alanay, Yves Alembik, Navid Almadani, Helen V. Firth, Mohamad Hasan Kariminejad, Chong Ae Kim, Kathryn Leask, Melissa K. Maisenbacher, Ellen Moran, John Pappas, Paolo Prontera, Thomy de Ravel, J. P. Fryns, Elizabeth Sweeney, Alan Fryer, Sheila Unger, Louise C. Wilson, Ralph S. Lachman, David L. Rimoin, Daniel H. Cohn, Deborah Krakow, Stephen P. Robertson

    Published 2006
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