Hasil Pencarian - Anushree Acharya

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  1. 1
    A Start Codon Variant in NOG Underlies Symphalangism and Ossicular Chain Malformations Affecting Both the Incus and the Stapes

    A Start Codon Variant in NOG Underlies Symphalangism and Ossicular Chain Malformations Affecting Both the Incus and the Stapes oleh Nathan R. Lindquist, Eric N. Appelbaum, Anushree Acharya, Jeffrey T. Vrabec, Suzanne M. Leal, Isabelle Schrauwen

    Diterbitkan 2019-01-01
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  2. 2
    Depression, malnutrition, and health-related quality of life among Nepali older patients

    Depression, malnutrition, and health-related quality of life among Nepali older patients oleh Saruna Ghimire, Binaya Kumar Baral, Buddhi Raj Pokhrel, Asmita Pokhrel, Anushree Acharya, Dipta Amatya, Prabisha Amatya, Shiva Raj Mishra

    Diterbitkan 2018-08-01
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  3. 3
    Identification of microduplications at Xp21.2 and Xq13.1 in neurodevelopmental disorders

    Identification of microduplications at Xp21.2 and Xq13.1 in neurodevelopmental disorders oleh Hannaleena Kokkonen, Auli Siren, Tuomo Määttä, Magda Kamila Kadlubowska, Anushree Acharya, Liz M. Nouel‐Saied, Suzanne M. Leal, Irma Järvelä, Isabelle Schrauwen

    Diterbitkan 2021-12-01
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  4. 4
    Autosomal recessive nonsyndromic hearing impairment in two Finnish families due to the population enriched CABP2 c.637+1G>T variant

    Autosomal recessive nonsyndromic hearing impairment in two Finnish families due to the population enriched CABP2 c.637+1G>T variant oleh Thashi Bharadwaj, Isabelle Schrauwen, Anushree Acharya, Liz M. Nouel‐Saied, Marja‐Leena Väisänen, Minna Kraatari, Elisa Rahikkala, Irma Jarvela, Jouko Kotimäki, Suzanne M. Leal

    Diterbitkan 2022-03-01
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  5. 5
    Novel digenic inheritance of PCDH15 and USH1G underlies profound non-syndromic hearing impairment

    Novel digenic inheritance of PCDH15 and USH1G underlies profound non-syndromic hearing impairment oleh Isabelle Schrauwen, Imen Chakchouk, Anushree Acharya, Khurram Liaqat, Irfanullah, University of Washington Center for Mendelian Genomics, Deborah A. Nickerson, Michael J. Bamshad, Khadim Shah, Wasim Ahmad, Suzanne M. Leal

    Diterbitkan 2018-07-01
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  6. 6
    A novel autosomal dominant GREB1L variant associated with non-syndromic hearing impairment in Ghana

    A novel autosomal dominant GREB1L variant associated with non-syndromic hearing impairment in Ghana oleh Samuel Mawuli Adadey, Elvis Twumasi Aboagye, Kevin Esoh, Anushree Acharya, Thashi Bharadwaj, Nicole S. Lin, Lucas Amenga-Etego, Gordon A. Awandare, Isabelle Schrauwen, Suzanne M. Leal, Ambroise Wonkam

    Diterbitkan 2022-11-01
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  7. 7
    Optical genome mapping unveils hidden structural variants in neurodevelopmental disorders

    Optical genome mapping unveils hidden structural variants in neurodevelopmental disorders oleh Isabelle Schrauwen, Yasmin Rajendran, Anushree Acharya, Susanna Öhman, Maria Arvio, Ritva Paetau, Auli Siren, Kristiina Avela, Johanna Granvik, Suzanne M. Leal, Tuomo Määttä, Hannaleena Kokkonen, Irma Järvelä

    Diterbitkan 2024-05-01
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  8. 8
    Human Papillomavirus (HPV) Infection: Molecular Epidemiology, Genotyping, Seroprevalence and Associated Risk Factors among Arab Women in Qatar.

    Human Papillomavirus (HPV) Infection: Molecular Epidemiology, Genotyping, Seroprevalence and Associated Risk Factors among Arab Women in Qatar. oleh Asha A Elmi, Devendra Bansal, Anushree Acharya, Sini Skariah, Soha R Dargham, Laith J Abu-Raddad, Nady Mohamed-Nady, Paul Amuna, Asma A J Al-Thani, Ali A Sultan

    Diterbitkan 2017-01-01
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  9. 9
    Antimicrobial susceptibility and molecular epidemiology of extended-spectrum beta-lactamase-producing Enterobacteriaceae from intensive care units at Hamad Medical Corporation, Qatar

    Antimicrobial susceptibility and molecular epidemiology of extended-spectrum beta-lactamase-producing Enterobacteriaceae from intensive care units at Hamad Medical Corporation, Qat... oleh Mazen A Sid Ahmed, Devendra Bansal, Anushree Acharya, Asha A. Elmi, Jemal M Hamid, Abuelhassan M Sid Ahmed, Prem Chandra, Emad Ibrahim, Ali A Sultan, Sanjay Doiphode, Naser Eldin Bilal, Anand Deshmukh

    Diterbitkan 2016-02-01
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  10. 10
    Long‐read whole‐genome sequencing for the genetic diagnosis of dystrophinopathies

    Long‐read whole‐genome sequencing for the genetic diagnosis of dystrophinopathies oleh Zhiying Xie, Chengyue Sun, Siwen Zhang, Yilin Liu, Meng Yu, Yiming Zheng, Lingchao Meng, Anushree Acharya, Diana M Cornejo‐Sanchez, Gao Wang, Wei Zhang, Isabelle Schrauwen, Suzanne M. Leal, Zhaoxia Wang, Yun Yuan

    Diterbitkan 2020-10-01
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  11. 11
    Exome sequencing of families from Ghana reveals known and candidate hearing impairment genes

    Exome sequencing of families from Ghana reveals known and candidate hearing impairment genes oleh Ambroise Wonkam, Samuel Mawuli Adadey, Isabelle Schrauwen, Elvis Twumasi Aboagye, Edmond Wonkam-Tingang, Kevin Esoh, Kalinka Popel, Noluthando Manyisa, Mario Jonas, Carmen deKock, Victoria Nembaware, Diana M. Cornejo Sanchez, Thashi Bharadwaj, Abdul Nasir, Jenna L. Everard, Magda K. Kadlubowska, Liz M. Nouel-Saied, Anushree Acharya, Osbourne Quaye, Geoffrey K. Amedofu, Gordon A. Awandare, Suzanne M. Leal

    Diterbitkan 2022-04-01
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