Mouna Lemaamer

1PUBLICATIONS
4CO-AUTHORS
Developmental genetics (incl. sex determination)
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Publications (1)

|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

Khadija Belcadi Abassi

1 joint publications

Abdelilah Radi

1 joint publications

Rachid Abilkassem