Fatin Fahad Al Denaini

1PUBLICATIONS
2CO-AUTHORS
Developmental genetics (incl. sex determination)
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Publications (1)

|Oct 06, 2022
Pathogenic Novel Heterozygous Variant c.1076c>T p. (Ser359Phe) chr1: 120512166 in NOTCH2 Gene, Type 2 Alagille Syndrome Causing Neonatal Cholestasis: A Case Report.

Mohammed Shahab Uddin, Saleh Al Fulayyih, Fatin Fahad Al Denaini

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Frequent Collaborators

1 joint publications

Mohammed Shahab Uddin

1 joint publications

Saleh Al Fulayyih