Search Results - Rafiullah, Rafiullah

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  1. 1
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    Biallelic variants in CSMD1 are implicated in a neurodevelopmental disorder with intellectual disability and variable cortical malformations by Werren, Elizabeth A. (Author) , Peirent, Emily R. (Author) , Jantti, Henna (Author) , Guxholli, Alba (Author) , Srivastava, Kinshuk Raj (Author) , Orenstein, Naama (Author) , Narayanan, Vinodh (Author) , Wiszniewski, Wojciech (Author) , Dawidziuk, Mateusz (Author) , Gawlinski, Pawel (Author) , Umair, Muhammad (Author) , Khan, Amjad (Author) , Khan, Shahid Niaz (Author) , Geneviève, David (Author) , Lehalle, Daphné (Author) , van Gassen, K. L. I. (Author) , Giltay, Jacques C. (Author) , Oegema, Renske (Author) , van Jaarsveld, Richard H. (Author) , Rafiullah, Rafiullah (Author) , Rappold, Gudrun (Author) , Rabin, Rachel (Author) , Pappas, John G. (Author) , Wheeler, Marsha M. (Author) , Bamshad, Michael J. (Author) , Tsan, Yao-Chang (Author) , Johnson, Matthew B. (Author) , Keegan, Catherine E. (Author) , Srivastava, Anshika (Author) , Bielas, Stephanie L. (Author) ,


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  2. 2
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    Sex hormones regulate SHANK expression by Berkel, Simone (Author) , Eltokhi, Ahmed (Author) , Fröhlich, Henning (Author) , Porras-Gonzalez, Diana (Author) , Rafiullah, Rafiullah (Author) , Sprengel, Rolf (Author) , Rappold, Gudrun (Author) ,


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  3. 3
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    A novel homozygous ARL13B variant in patients with Joubert syndrome impairs its guanine nucleotide-exchange factor activity by Rafiullah, Rafiullah (Author) , Blum, Martin (Author) , Berkel, Simone (Author) , Paramasivam, Nagarajan (Author) , Rappold, Gudrun (Author) ,


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  4. 4
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    Identification and characterization of genes underlying for intellectual disability and autism spectrum disorder by Rafiullah, Rafiullah (Author)

    2017

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  5. 5
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    Foxp1 expression is essential for sex-specific murine neonatal ultrasonic vocalization by Fröhlich, Henning (Author) , Rafiullah, Rafiullah (Author) , Abele, Sonja (Author) , Rappold, Gudrun (Author) ,


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  6. 6
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    Homozygous missense mutation in the LMAN2L gene segregates with intellectual disability in a large consanguineous Pakistani family by Rafiullah, Rafiullah (Author) , Aslamkhan, Muhammad (Author) , Paramasivam, Nagarajan (Author) , Thiel, Christian (Author) , Mustafa, Ghulam (Author) , Wiemann, Stefan (Author) , Schlesner, Matthias (Author) , Wade, Rebecca C. (Author) , Rappold, Gudrun (Author) , Berkel, Simone (Author) ,


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