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Page 1
Identification of novel mutations in Pakistani families with autosomal recessive retinitis pigmentosa.
Azam M, Collin RW, Malik A, Khan MI, Shah ST, Shah AA, Hussain A, Sadeque A, Arimadyo K, Ajmal M, Azam A, Qureshi N, Bokhari H, Strom TM, Cremers FP, Qamar R, den Hollander AI. Azam M, et al. Among authors: bokhari h. Arch Ophthalmol. 2011 Oct;129(10):1377-8. doi: 10.1001/archophthalmol.2011.290. Arch Ophthalmol. 2011. PMID: 21987686 No abstract available.
Homozygosity mapping identifies genetic defects in four consanguineous families with retinal dystrophy from Pakistan.
Khan MI, Ajmal M, Micheal S, Azam M, Hussain A, Shahzad A, Venselaar H, Bokhari H, de Wijs IJ, Hoefsloot LH, Waheed NK, Collin RW, den Hollander AI, Qamar R, Cremers FP. Khan MI, et al. Among authors: bokhari h. Clin Genet. 2013 Sep;84(3):290-3. doi: 10.1111/cge.12039. Epub 2012 Nov 7. Clin Genet. 2013. PMID: 23134348 No abstract available.
HriGFP Novel Flourescent Protein: Expression and Applications.
Saeed S, Mehreen H, Gerlevik U, Tariq A, Manzoor S, Noreen Z, Sezerman U, Bokhari H. Saeed S, et al. Among authors: bokhari h. Mol Biotechnol. 2020 May;62(5):280-288. doi: 10.1007/s12033-020-00243-1. Mol Biotechnol. 2020. PMID: 32108285
112 results