1. Application of spore morphology to solve identification problems in certain species of family Dryopteridaceae from Malakand Division, Pakistan. Issue 8 (3rd March 2021) Authors: Shah, Syed N.; Ahmad, Mushtaq; Zafar, Muhammad; Hadi, Fazal; Khan, Muhammad N.; Noor, Adil; Malik, Khafsa; Rashid, Neelam; Kamal, Asif; Iqbal, Majid; Hussain, Murtaza Journal: Microscopy research and technique Issue: Volume 84:Issue 8(2021) Page Start: 1897 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. Determination of cefixime in pure form, in pharmaceutical products and biological samples through fluorescence quenching of eosin Y. (18th November 2020) Authors: Khan, Muhammad N.; Irum, ; Mursaleen, Muhammad Journal: Luminescence Issue: Volume 36:Number 2(2021) Page Start: 515 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. Genetic causes of MCPH in consanguineous Pakistani families. Issue 6 (8th November 2015) Authors: Kraemer, Nadine; Picker‐Minh, Sylvie; Abbasi, Ansar A.; Fröhler, Sebastian; Ninnemann, Olaf; Khan, Muhammad N.; Ali, Ghazanfar; Chen, Wei; Kaindl, Angela M. Journal: Clinical genetics Issue: Volume 89:Issue 6(2016) Page Start: 744 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
4. Identification of a novel homozygous TRAPPC9 gene mutation causing non‐syndromic intellectual disability, speech disorder, and secondary microcephaly. Issue 8 (14th October 2017) Authors: Abbasi, Ansar A.; Blaesius, Kathrin; Hu, Hao; Latif, Zahid; Picker‐Minh, Sylvie; Khan, Muhammad N.; Farooq, Sundas; Khan, Muzammil A.; Kaindl, Angela M. Journal: American journal of medical genetics Issue: Volume 174:Issue 8(2017) Page Start: 839 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
5. Identification of novel mutation in the HR gene responsible for atrichia with papular lesions in a Pakistani family. Issue 11 (20th September 2013) Authors: Ahmed, Muhammad S.; Rauf, Sobiah; Naeem, Muhammad; Khan, Muhammad N.; Mir, Asif Journal: Journal of dermatology Issue: Volume 40:Issue 11(2013) Page Start: 927 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
6. Mutations in the tRNA methyltransferase 1 gene TRMT1 cause congenital microcephaly, isolated inferior vermian hypoplasia and cystic leukomalacia in addition to intellectual disability. Issue 11 (5th October 2018) Authors: Blaesius, Kathrin; Abbasi, Ansar A.; Tahir, Tufail H.; Tietze, Anna; Picker‐Minh, Sylvie; Ali, Ghazanfar; Farooq, Sundas; Hu, Hao; Latif, Zahid; Khan, Muhammad N.; Kaindl, Angela Journal: American journal of medical genetics Issue: Volume 176:Issue 11(2018) Page Start: 2517 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
7. New environmentally attractive separation technology for flue gas mixture. (17th November 2018) Authors: Animasahun, Olamide H.; Khan, Muhammad N.; Peters, Cornelis J. Journal: Molecular physics Issue: Volume 116:Number 21/22(2018) Page Start: 3434 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
8. The Limited Role of Microbiological Culture and Sensitivity in the Management of Superficial Soft Tissue Abscesses. (2006) Authors: Khan, Muhammad N.; Vidya, Raghavan; Lee, Richard E. Journal: TheScientificWorldjournal Issue: Volume 6(2006) Page Start: 1118 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗