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Extending the ophthalmological phenotype of Galloway-Mowat syndrome with distinct retinal dysfunction: a report and review of ocular findings
by
Al-Rakan, Maha A
,
Abothnain, Manal D
,
Alrifai, Muhammad T
,
Alfadhel, Majid
Published in
BMC ophthalmology
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Further delineation of Wiedemann‐Rautenstrauch syndrome linked with POLR3A
by
Khan, Amjad
,
Al Shamsi, Bushra
,
Al Shehhi, Maryam
,
Kashgari, Amna A.
,
Al Balushi, Aaisha
,
Al Dihan, Fahad A.
,
Alghamdi, Mohannad A.
,
Manal, Abothnain
,
González‐Álvarez, Ana C.
,
Arold, Stefan T.
,
Eyaid, Wafaa
Published in
Molecular genetics & genomic medicine
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