Hasil Pencarian - Anna Rajab

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  1. 1
    Genetic disruption of WASHC4 drives endo-lysosomal dysfunction and cognitive-movement impairments in mice and humans

    Genetic disruption of WASHC4 drives endo-lysosomal dysfunction and cognitive-movement impairments in mice and humans oleh Jamie L Courtland, Tyler WA Bradshaw, Greg Waitt, Erik J Soderblom, Tricia Ho, Anna Rajab, Ricardo Vancini, Il Hwan Kim, Scott H Soderling

    Diterbitkan 2021-03-01
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  2. 2
    Fatal cardiac arrhythmia and long-QT syndrome in a new form of congenital generalized lipodystrophy with muscle rippling (CGL4) due to PTRF-CAVIN mutations.

    Fatal cardiac arrhythmia and long-QT syndrome in a new form of congenital generalized lipodystrophy with muscle rippling (CGL4) due to PTRF-CAVIN mutations. oleh Anna Rajab, Volker Straub, Liza J McCann, Dominik Seelow, Raymonda Varon, Rita Barresi, Anne Schulze, Barbara Lucke, Susanne Lützkendorf, Mohsen Karbasiyan, Sebastian Bachmann, Simone Spuler, Markus Schuelke

    Diterbitkan 2010-03-01
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  3. 3
    Repository of mutations from Oman: The entry point to a national mutation database [version 1; referees: 2 approved]

    Repository of mutations from Oman: The entry point to a national mutation database [version 1; referees: 2 approved] oleh Anna Rajab, Nishath Hamza, Salma Al Harasi, Fatma Al Lawati, Una Gibbons, Intesar Al Alawi, Karoline Kobus, Suha Hassan, Ghariba Mahir, Qasim Al Salmi, Barend Mons, Peter Robinson

    Diterbitkan 2015-09-01
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  4. 4
    DALIA- a comprehensive resource of Disease Alleles in Arab population.

    DALIA- a comprehensive resource of Disease Alleles in Arab population. oleh Aastha Vatsyayan, Parul Sharma, Shrey Gupta, Sumiti Sandhu, Seetha Lakshmi Venu, Vandana Sharma, Bouabid Badaoui, Kaidi Azedine, Serti Youssef, Anna Rajab, Alaaeldin Fayez, Seema Madinur, Anop Ranawat, Kavita Pandhare, Srinivasan Ramachandran, Sridhar Sivasubbu, Vinod Scaria

    Diterbitkan 2021-01-01
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