Khadija Belcadi Abassi

2PUBLICATIONS
4CO-AUTHORS
Cardiovascular medicine and haematology not elsewhere classifiedDevelopmental genetics (incl. sex determination)
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Publications (2)

|Apr 16, 2026
Type 3 Von Willebrand disease: two clinical cases of a rare disorder.

|Mar 11, 2026
Novel ANKRD11 Mutation in KBG Syndrome: A diagnostic triad of hearing loss, radiological macrodontia and artificial intelligence-assisted facial phenotyping.

Azzeddine Laaraje, Khadija Belcadi Abassi, Mouna Lemaamer

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Frequent Collaborators

1 joint publications

Azzeddine Laaraje

1 joint publications

Mouna Lemaamer

1 joint publications

Abdelilah Radi

1 joint publications

Rachid Abilkassem