Novel R225C variant identified in the HGD gene in Jordanian patients with alkaptonuria
Mwafi, Nesrin R., Ali, Dema A., Khalil, Raida W., Alsbou', Ibrahim N., Saraireh, Ahmad M.
Published in AIMS molecular science (01.03.2021)
Published in AIMS molecular science (01.03.2021)
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Detection of novel LAMA3 mutation in Herlitz junctional epidermolysis bullosa in a Jordanian family: Epidermolysis bullosa: a novel mutation
Badran, Eman F., Battah, Hamdi A., Akl, Kamal F, Khalil, Raida W., Al Amori, Iyad
Published in Australasian journal of dermatology (01.08.2013)
Published in Australasian journal of dermatology (01.08.2013)
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Multiple sclerosis in Arabs in Jordan
Al-Din, A.S.Najim, El-Khateeb, M., Kurdi, A., Mubaidin, A., Wriekat, A., Al-Shehab, Ahmed, Khalil, Raida W.
Published in Journal of the neurological sciences (01.08.1995)
Published in Journal of the neurological sciences (01.08.1995)
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Journal Article
Epidemiology of multiple sclerosis in Arabs in Jordan: a comparative study between Jordanians and Palestinians
Najim Al-Din, Amir S., Kurdi, Ashraf, Mubaidin, Ammar, El-Khateeb, Mohammed, Khalil, Raida W., Wriekat, Abdel-Latif
Published in Journal of the neurological sciences (01.02.1996)
Published in Journal of the neurological sciences (01.02.1996)
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