Ghent University Academic Bibliography

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Novel FRMD7 mutations and genomic rearrangement expand the molecular pathogenesis of X-linked idiopathic infantile nystagmus

Basamat Almoallem Mohammed (UGent) , Miriam Bauwens (UGent) , SOPHIE WALRAEDT (UGent) , Patricia Delbeke, Julie De Zaeytijd (UGent) , Bart Leroy (UGent) and Elfride De Baere (UGent)

(2015) BeMGI Annual meeting, Abstracts.
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- Conference Paper
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Novel FRMD7 mutations and genomic rearrangement expand the molecular pathogenesis of X-linked idiopathic infantile nystagmus

Basamat Almoallem Mohammed (UGent) , Miriam Bauwens (UGent) , SOPHIE WALRAEDT (UGent) , Patricia Delbeke, Julie De Zaeytijd (UGent) , Bart Leroy (UGent) and Elfride De Baere (UGent)

(2015) INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE. 56(7).
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Novel FRMD7 mutations and genomic rearrangement expand the molecular pathogenesis of X-linked idiopathic infantile nystagmus

Basamat Almoallem Mohammed (UGent) , Miriam Bauwens (UGent) , SOPHIE WALRAEDT (UGent) , Patricia Delbeke, Julie De Zaeytijd (UGent) , Philippe Kestelyn (UGent) , Françoise Meire, Sandra Janssens (UGent) , Caroline Van Cauwenbergh (UGent) , Hannah Verdin (UGent) , et al.

(2015) INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE. 56(3). p.1701-1710
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Novel and known FRMD7 mutations and copy number variation in Belgian patients with X-linked idiopathic infantile nystagmus

Basamat Almoallem Mohammed (UGent) , Miriam Bauwens (UGent) , SOPHIE WALRAEDT (UGent) , Patricia Delbeke, Julie De Zaeytijd (UGent) , Bart Leroy (UGent) and Elfride De Baere (UGent)

(2014) Translational genetics : from cage over bench to bed.

Academic Bibliography

Novel FRMD7 mutations and genomic rearrangement expand the molecular pathogenesis of X-linked idiopathic infantile nystagmus

Novel FRMD7 mutations and genomic rearrangement expand the molecular pathogenesis of X-linked idiopathic infantile nystagmus

Novel FRMD7 mutations and genomic rearrangement expand the molecular pathogenesis of X-linked idiopathic infantile nystagmus

Novel and known FRMD7 mutations and copy number variation in Belgian patients with X-linked idiopathic infantile nystagmus

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