Thashi Bharadwaj - Search Results

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Bi-Allelic Novel Variants in CLIC5 Identified in a Cameroonian Multiplex Family with Non-Syndromic Hearing Impairment.

Wonkam-Tingang E, Schrauwen I, Esoh KK, Bharadwaj T, Nouel-Saied LM, Acharya A, Nasir A, Adadey SM, Mowla S, Leal SM, Wonkam A. Wonkam-Tingang E, et al. Among authors: bharadwaj t. Genes (Basel). 2020 Oct 23;11(11):1249. doi: 10.3390/genes11111249. Genes (Basel). 2020. PMID: 33114113 Free PMC article.

Practical approach to the genetic diagnosis of unsolved dystrophinopathies: a stepwise strategy in the genomic era.

Xie Z, Sun C, Liu Y, Yu M, Zheng Y, Meng L, Wang G, Cornejo-Sanchez DM, Bharadwaj T, Yan J, Zhang L, Pineda-Trujillo N, Zhang W, Leal SM, Schrauwen I, Wang Z, Yuan Y. Xie Z, et al. Among authors: bharadwaj t. J Med Genet. 2020 Sep 25:jmedgenet-2020-107113. doi: 10.1136/jmedgenet-2020-107113. Online ahead of print. J Med Genet. 2020. PMID: 32978268

Autosomal Dominantly Inherited GREB1L Variants in Individuals with Profound Sensorineural Hearing Impairment.

Schrauwen I, Liaqat K, Schatteman I, Bharadwaj T, Nasir A, Acharya A, Ahmad W, Van Camp G, Leal SM. Schrauwen I, et al. Among authors: bharadwaj t. Genes (Basel). 2020 Jun 23;11(6):687. doi: 10.3390/genes11060687. Genes (Basel). 2020. PMID: 32585897 Free PMC article.

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