Fatimah Mouayed AlJishi

2PUBLICATIONS
1CO-AUTHORS
Developmental genetics (incl. sex determination)Major global burdens of disease
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Publications (2)

|Oct 02, 2025
Identifying 17-β-HSD3 Deficiency in Patients with Karyotype 46,XY Misdiagnosed with Androgen Insensitivity Syndrome: A Pediatric Case Report.

Beshaier Almulhem, Fatimah Mouayed AlJishi, Mohammad Al-Qahtani

|May 20, 2017
Glucose-6-phosphate dehydrogenase deficiency induced haemolysis in a woman with newly diagnosed diabetes after normalisation of hyperglycaemia.

F ALjishi, M ALDarwish

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Frequent Collaborators

1 joint publications

Beshaier Almulhem