1. A homozygous potentially pathogenic variant in the PAXBP1 gene in a large family with global developmental delay and myopathic hypotonia. Issue 6 (15th September 2017) Authors: Alharby, E.; Albalawi, A.M.; Nasir, A.; Alhijji, S.A.; Mahmood, A.; Ramzan, K.; Abdusamad, F.; Aljohani, A.; Abdelsalam, O.; Eldardear, A.; Basit, S. Journal: Clinical genetics Issue: Volume 92:Issue 6(2017) Page Start: 579 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. Developmental dysplasia of the hip: usefulness of next generation genomic tools for characterizing the underlying genes – a mini review. Issue 1 (4th March 2016) Authors: Basit, S.; Hannan, M. A.; Khoshhal, K. I. Journal: Clinical genetics Issue: Volume 90:Issue 1(2016) Page Start: 16 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. E1. Risk of chronic hypertension in women with a history of hypertensive disorders of pregnancy – a nationwide cohort study. (12th August 2016) Authors: Behrens, I.; Basit, S.; Melbye, M.; Lykke, J. A.; Wohlfahrt, J.; Bundgaard, H.; Thilaganathan, B.; Boyd, H. A. Journal: Journal of maternal-fetal & neonatal medicine Issue: Volume 29(2016)Supplement 2 Page Start: 21 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
4. Exome sequencing revealed a novel splice site variant in the ALX1 gene underlying frontonasal dysplasia. Issue 3 (12th July 2016) Authors: Ullah, A.; Kalsoom, U.‐E; Umair, M.; John, P.; Ansar, M.; Basit, S.; Ahmad, W. Journal: Clinical genetics Issue: Volume 91:Issue 3(2017) Page Start: 494 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
5. First direct evidence of involvement of a homozygous loss‐of‐function variant in the EPS15L1 gene underlying split‐hand/split‐foot malformation. Issue 3 (25th January 2018) Authors: Umair, M.; Ullah, A.; Abbas, S.; Ahmad, F.; Basit, S.; Ahmad, W. Journal: Clinical genetics Issue: Volume 93:Issue 3(2018) Page Start: 699 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
6. Genetics of human isolated hereditary hair loss disorders. (22nd November 2014) Authors: Basit, S.; Khan, S.; Ahmad, W. Journal: Clinical genetics Issue: Volume 88:Number 3(2015:Sep.) Page Start: 203 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
7. Genetics of human isolated hereditary nail disorders. (1st October 2015) Authors: Khan, S.; Basit, S.; Habib, R.; Kamal, A.; Muhammad, N.; Ahmad, W. Journal: British journal of dermatology Issue: Volume 173:Number 4(2015:Oct.) Page Start: 922 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
8. Genetics of human isolated hereditary nail disorders. (8th September 2015) Authors: Khan, S.; Basit, S.; Habib, R.; Kamal, A.; Muhammad, N.; Ahmad, W. Journal: British journal of dermatology Issue: Volume 173:Number 4(2015:Oct.) Page Start: 922 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
9. Influence of reinforcement arrangement details on mechanical behavior of precast concrete barrier with loop connection. (October 2020) Authors: Basit, S.; Maki, T.; Mutsuyoshi, H.; Ishihara, Y.; Tajima, H. Journal: Structures Issue: Volume 27(2020) Page Start: 1682 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
10. Novel autosomal recessive LAMA3 and PLEC variants underlie junctional epidermolysis bullosa generalized intermediate and epidermolysis bullosa simplex with muscular dystrophy in two consanguineous families. (23rd May 2018) Authors: Ahmad, F.; Shah, K.; Umair, M.; Jan, A.; Irfanullah, ; Khan, S.; Muhammad, D.; Basit, S.; Wakil, S. M.; Ramzan, K.; Ahmad, W. Journal: Clinical and experimental dermatology Issue: Volume 43:Number 6(2018) Page Start: 752 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗