1. Extending the spectrum of CLRN1‐ and ABCA4‐associated inherited retinal dystrophies caused by novel and recurrent variants using exome sequencing. Issue 3 (22nd January 2020) Authors: Abu‐Ameerh, Mohammed; Mohammad, Hashim; Dardas, Zain; Barham, Raghda; Ali, Dema; Bijawi, Maysa; Tawalbeh, Mohamed; Amr, Sami; Hatmal, Ma'mon M.; Al‐Bdour, Muawyah; Awidi, Abdalla; Azab, Belal Journal: Molecular genetics & genomic medicine Issue: Volume 8:Issue 3(2020) Page Start: n/a Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. Variant Analysis of Alkaptonuria Families with Significant Founder Effect in Jordan. (11th March 2021) Authors: Khalil, Raida; Ali, Dema; Mwafi, Nesrin; Alsaraireh, Arwa; Obeidat, Loiy; Albsoul, Eman; Al Sbou', Ibrahim Other Names: He Jing Academic Editor. Journal: BioMed research international Issue: Volume 2021(2021) Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗