Resultados da busca - Riazuddin, Saima

Some Deafness-Causing Mutations Can Be Silenced with the Appropriate Gene Partner por Wilcox, Edward, Riazuddin, Saima, Riazuddin, Sheikh

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Usher proteins in inner ear structure and function por Ahmed, Zubair M., Frolenkov, Gregory I., Riazuddin, Saima

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Delineation of Homozygous Variants Associated with Prelingual Sensorineural Hearing Loss in Pakistani Families por Noman, Muhammad, Ishaq, Rafaqat, Bukhari, Shazia A., Ahmed, Zubair M., Riazuddin, Saima

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Identification of Hearing Loss-Associated Variants of PTPRQ, MYO15A, and SERPINB6 in Pakistani Families por Mahmood, Umair, Bukhari, Shazia A., Ali, Muhammad, Ahmed, Zubair M., Riazuddin, Saima

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Delineation of Novel Compound Heterozygous Variants in LTBP2 Associated with Juvenile Open Angle Glaucoma por Saeedi, Osamah, Yousaf, Sairah, Tsai, Joby, Palmer, Kathleen, Riazuddin, Saima, Ahmed, Zubair M.

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Molecular characterization of SLC24A5 variants and evaluation of Nitisinone treatment efficacy in a zebrafish model of OCA6 por Yousaf, Sairah, Sethna, Saumil, Chaudhary, Muhammad A., Shaikh, Rehan S., Riazuddin, Saima, Ahmed, Zubair M.

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USH1K, a novel locus for type I Usher syndrome, maps to chromosome 10p11.21-q21.1 por Jaworek, Thomas J., Bhatti, Rashid, Latief, Naureen, Khan, Shaheen N., Riazuddin, Saima, Ahmed, Zubair M

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Genomics of Otitis Media (OM): Molecular Genetics Approaches to Characterize Disease Pathophysiology por Giese, Arnaud P. J., Ali, Saadat, Isaiah, Amal, Aziz, Ishrat, Riazuddin, Saima, Ahmed, Zubair M.

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USH1H, a novel locus for type I Usher syndrome, maps to chromosome 15q22-23 por Ahmed, Zubair M, Riazuddin, Saima, Khan, Shaheen N, Friedman, Penelope L, Riazuddin, Sheikh, Friedman, Thomas B

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Biallelic in-frame deletion of SOX4 is associated with developmental delay, hypotonia and intellectual disability por Ghaffar, Amama, Rasheed, Faiza, Rashid, Muhammad, van Bokhoven, Hans, Ahmed, Zubair M., Riazuddin, Sheikh, Riazuddin, Saima

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Novel Mutations in CLPP, LARS2, CDH23, and COL4A5 Identified in Familial Cases of Prelingual Hearing Loss por Zafar, Saba, Shahzad, Mohsin, Ishaq, Rafaqat, Yousaf, Ayesha, Shaikh, Rehan S., Akram, Javed, Ahmed, Zubair M., Riazuddin, Saima

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Biallelic Variants in EPHA2 Identified in Three Large Inbred Families with Early-Onset Cataract por Jarwar, Priya, Sheikh, Shakeel Ahmed, Waryah, Yar Muhammad, Ujjan, Ikram Uddin, Riazuddin, Saima, Waryah, Ali Muhammad, Ahmed, Zubair M.

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Novel Homozygous Missense Variant in GJA3 Connexin Domain Causing Congenital Nuclear and Cortical Cataracts por Hassan, Abdullah Y., Yousaf, Sairah, Levin, Moran R., Saeedi, Osamah J., Riazuddin, Saima, Alexander, Janet L., Ahmed, Zubair M.

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Mutations in Diphosphoinositol-Pentakisphosphate Kinase PPIP5K2 are associated with hearing loss in human and mouse por Yousaf, Rizwan, Gu, Chunfang, Ahmed, Zubair M., Khan, Shaheen N., Friedman, Thomas B., Riazuddin, Sheikh, Shears, Stephen B., Riazuddin, Saima

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DFNB86, a novel autosomal recessive nonsyndromic deafness locus on chromosome 16p13.3 por Ali, Rana A., Rehman, Atteeq U., Khan, Shaheen N., Husnain, Tayyab, Riazuddin, Sheikh, Friedman, Thomas B., Ahmed, Zubair M., Riazuddin, Saima

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A New Locus for Nonsyndromic Deafness DFNB51 Maps to Chromosome 11p13-p12 por Shaikh, Rehan Sadiq, Ramzan, Khushnooda, Nazli, Sabiha, Sattar, Sameera, Khan, Shaheen N., Riazuddin, Saima, Ahmed, Zubair M., Friedman, Thomas B., Riazuddin, Sheikh

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Phenotypic variability of CLDN14 mutations causing DFNB29 hearing loss in the Pakistani population por Bashir, Zil-e-Huma, Latief, Noreen, Belyantseva, Inna A., Iqbal, Farheena, Riazuddin, S. Amer, Khan, Shaheen N., Friedman, Thomas B., Riazuddin, Sheikh, Riazuddin, Saima

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A novel CHST3 allele associated with Spondyloepiphyseal dysplasia and hearing loss in Pakistani kindred por Waryah, Ali M., Shahzad, Mohsin, Shaikh, Hina, Sheikh, Shakeel A., Channa, Naseem A., Hufnagel, Robert B., Makhdoom, Asadullah, Riazuddin, Saima, Ahmed, Zubair M.

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Gene structure and mutant alleles of PCDH15: nonsyndromic deafness DFNB23 and type 1 Usher syndrome por Ahmed, Zubair M., Riazuddin, Saima, Aye, Sandar, Ali, Rana A., Venselaar, Hanka, Anwar, Saima, Belyantseva, Polina P., Qasim, Muhammad, Riazuddin, Sheikh, Friedman, Thomas B.

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Identification and clinical characterization of Hermansky-Pudlak syndrome alleles in the Pakistani population por Yousaf, Sairah, Shahzad, Mohsin, Tasleem, Kausar, Sheikh, Shakeel A., Tariq, Nabeela, Shabbir, Asra S., Ali, Muhammad, Waryah, Ali M., Shaikh, Rehan S., Riazuddin, Saima, Ahmed, Zubair M.

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