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Journal of Human Genetics|March 17, 2009
SLC26A4 mutation spectrum associated with DFNB4 deafness and Pendred's syndrome in PakistanisSaima Anwar, Saima Riazuddin, Zubair M Ahmed, et al.
Human Genetics|February 16, 2005
DFNB48, a new nonsyndromic recessive deafness locus, maps to chromosome 15q23-q25.1Jamil Ahmad, Shaheen N Khan, Shahid Y Khan, et al.
Human Genetics|September 29, 2005
Severe autosomal recessive retinitis pigmentosa maps to chromosome 1p13.3-p21.2 between D1S2896 and D1S457 but outside ABCA4Qingjiong Zhang, Fareeha Zulfiqar, Xueshan Xiao, et al.
Virology Journal|August 25, 2009
Nucleotide identity and variability among different Pakistani hepatitis C virus isolatesMuhammad Idrees, Sadia Butt, Zunaira Awan, et al.
Scientific Data|September 12, 2018
Whole genome sequencing data for two individuals of Pakistani descentShahid Y Khan, Firoz Kabir, Oussama M'Hamdi, et al.
Clinical Genetics|March 8, 2024
Homozygous novel truncating variant of CLPP associated with severe Perrault syndromeRabia Faridi, Pamela Stratton, Noemi Salmeri, et al.
The British Journal of Ophthalmology|June 12, 2010
Nonsense mutation in MERTK causes autosomal recessive retinitis pigmentosa in a consanguineous Pakistani familyAmber Shahzadi, S Amer Riazuddin, Shahbaz Ali, et al.
Human Genetics|August 23, 2008
Gene structure and mutant alleles of PCDH15: nonsyndromic deafness DFNB23 and type 1 Usher syndromeZubair M Ahmed, Saima Riazuddin, Sandar Aye, et al.
International Journal of Biological Macromolecules|February 9, 2023
Zinc oxide loaded chitosan-elastin-sodium alginate nanocomposite gel using freeze gelation for enhanced adipose stem cell proliferation and antibacterial propertiesAmna Ramzan, Azra Mehmood, Ramla Ashfaq, et al.
European Journal of Human Genetics : EJHG|October 16, 2008
Identification of two new mutations in the GPR98 and the PDE6B genes segregating in a Tunisian familyMounira Hmani-Aifa, Zeineb Benzina, Fareeha Zulfiqar, et al.
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