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Willows, Jamie.
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Journal articles
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Case report: investigation and molecular genetic diagnosis of familial hypomagnesaemia.
Willows, Jamie.
F1000 Research Ltd.
2019-01-01
Case report: investigation and molecular genetic diagnosis of familial hypomagnesaemia.
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Willows, Jamie.
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English
(1)
Category
Journal articles
(1)
Subject
Arrhythmias, Cardiac--Oman
(1)
Molecular genetics--Oman
(1)
Author
(-)
Willows, Jamie.
(1)
, .Othman IbrahimAl-Shihy
(1)
, Abbas Abdul HadiAl-Lawati
(1)
Al-Araimiyah, .Amna Salim
(1)
Al-Bahri, Osama Hashel Salim.
(1)
Al-Baqlani, Said Ali.
(1)
Al-Busaidiyah, Zakia Nasser.
(1)
Al-Dhahliyah, Buthaina Saif
(1)
Al-Faleh, Khalid M.
(1)
Al-Futaisi, Abdullah.
(1)
Al-Hashamiyah, Zainab Salam Suleiman.
(1)
Al-Khaliliyah, Shafiya Ahmed Hilal.
(1)
Al-Lamkyah, .Ruwaida Naseer
(1)
Al-Lawatiyah, Afaf Ali Juma
(1)
Al-Lawatiyah, Fatma.
(1)
Al-Lawatiyah, Najla.
(1)
Al-Mahrouqiyah, Sara Hamed Mohamed.
(1)
Al-Maqbaliyah, Salima R. S.
(1)
Al-Mazrouaiyah, .Safa Said Saif
(1)
Al-Rawahiyah, Wafaa Ahmed Abdullah.
(1)
Al-Rubkhiyah, Muna Ali Masoud.
(1)
Al-Sharjyah, Nawal Khalfan.
(1)
Al-Subhi, Ali Masoud.
(1)
Basak, Saroma.
(1)
Benda, Petr.
(1)
Bererhi, Hadia.
(1)
Bini Araba, Asma Saif
(1)
Elmehdawi, Rafik R.
(1)
Ince, Yavuz.
(1)
Jensen, Marlene M.
(1)
Koul, Rashan.
(1)
Mahapatra, Mana.
(1)
Rahhal, Nour Al Huda
(1)
Van der Nest, M. A.
(1)
Publisher
F1000 Research Ltd
(1)
sfy39587stp18