1. Founder mutation in dystonin‐e underlying autosomal recessive epidermolysis bullosa simplex in Kuwait. (1st February 2015) Authors: Takeichi, T.; Nanda, A.; Liu, L.; Aristodemou, S.; McMillan, J.R.; Sugiura, K.; Akiyama, M.; Al‐Ajmi, H.; Simpson, M.A.; McGrath, J.A. Journal: British journal of dermatology Issue: Volume 172:Number 2(2015:Feb.) Page Start: 527 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. Founder mutation in dystonin‐e underlying autosomal recessive epidermolysis bullosa simplex in Kuwait. (30th December 2014) Authors: Takeichi, T.; Nanda, A.; Liu, L.; Aristodemou, S.; McMillan, J.R.; Sugiura, K.; Akiyama, M.; Al‐Ajmi, H.; Simpson, M.A.; McGrath, J.A. Journal: British journal of dermatology Issue: Volume 172:Number 2(2015:Feb.) Page Start: 527 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. Incontinentia pigmenti in a father and daughter. (1st November 2016) Authors: Rashidghamat, E.; Hsu, C.K.; Nanda, A.; Liu, L.; Al‐Ajmi, H.; McGrath, J.A. Journal: British journal of dermatology Issue: Volume 175:Number 5(2016) Page Start: 1059 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
4. Incontinentia pigmenti in a father and daughter. (24th July 2016) Authors: Rashidghamat, E.; Hsu, C.K.; Nanda, A.; Liu, L.; Al‐Ajmi, H.; McGrath, J.A. Journal: British journal of dermatology Issue: Volume 175:Number 5(2016) Page Start: 1059 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
5. Syndromic inherited poikiloderma due to a de novo mutation in FAM111B. (1st February 2017) Authors: Takeichi, T.; Nanda, A.; Yang, H.‐S.; Hsu, C.‐K.; Lee, J.Y.‐Y.; Al‐Ajmi, H.; Akiyama, M.; Simpson, M.A.; McGrath, J.A. Journal: British journal of dermatology Issue: Volume 176:Number 2(2017) Page Start: 534 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
6. Syndromic inherited poikiloderma due to a de novo mutation in FAM111B. (22nd December 2016) Authors: Takeichi, T.; Nanda, A.; Yang, H.‐S.; Hsu, C.‐K.; Lee, J.Y.‐Y.; Al‐Ajmi, H.; Akiyama, M.; Simpson, M.A.; McGrath, J.A. Journal: British journal of dermatology Issue: Volume 176:Number 2(2017) Page Start: 534 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
7. Whole‐exome sequencing diagnosis of two autosomal recessive disorders in one family. (1st May 2015) Authors: Takeichi, T.; Nanda, A.; Aristodemou, S.; McMillan, J.R.; Lee, J.; Akiyama, M.; Al‐Ajmi, H.; Simpson, M.A.; McGrath, J.A. Journal: British journal of dermatology Issue: Volume 172:Number 5(2015:May) Page Start: 1407 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
8. Whole‐exome sequencing diagnosis of two autosomal recessive disorders in one family. (7th March 2015) Authors: Takeichi, T.; Nanda, A.; Aristodemou, S.; McMillan, J.R.; Lee, J.; Akiyama, M.; Al‐Ajmi, H.; Simpson, M.A.; McGrath, J.A. Journal: British journal of dermatology Issue: Volume 172:Number 5(2015:May) Page Start: 1407 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗