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B P Leroy

Showing results (21-30 of 36) with videos related to

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International Journal of Pediatric Otorhinolaryngology|November 5, 2010
Etiological diagnosis in the hearing impaired newborn: proposal of a flow chartE M R De Leenheer, S Janssens, E Padalko, et al.
Bulletin De La Societe Belge D'Ophtalmologie|June 14, 2014
Bifocal optic and facial nerve t-cell lymphomaA Van Hoey, A Shah, J De Zaeytijd, et al.
The British Journal of Radiology|February 25, 2006
Visceral and testicular calcifications as part of the phenotype in pseudoxanthoma elasticum: ultrasound findings in Belgian patients and healthy carriersO M Vanakker, D Voet, M Petrovic, et al.
Experimental Eye Research|December 21, 2005
Retinal vessel dilation following repletion of vitamin A deficiencyM Larsen, R Pedersen, N C B B Taarnhøj, et al.
Investigative Ophthalmology & Visual Science|October 29, 2000
Novel locus for autosomal recessive cone-rod dystrophy CORD8 mapping to chromosome 1q12-Q24S Khaliq, A Hameed, M Ismail, et al.
The British Journal of Ophthalmology|May 19, 2007
High beta-trace protein concentration in the fluid of an orbital cyst associated with bilateral colobomatous microphthalmosC E Decock, C M Breusegem, E H Van Aken, et al.
European Journal of Human Genetics : EJHG|January 1, 1996
Refined genetic and physical mapping of BPES type IIL Messiaen, B P Leroy, S De Bie, et al.
Clinical Genetics|April 19, 2003
The contribution of USH1C mutations to syndromic and non-syndromic deafness in the UKD C Blaydon, R F Mueller, T P Hutchin, et al.
Stem Cell Research|May 30, 2025
Generation of two iPSC lines (UGENTi003 and UGENTi004) from patients with intermediate rod-cone dystrophy carrying the c.[-123C>T;701G>A];[806_810del] variants in the RDH12 geneM Bouckaert, F Van Den Broeck, M Ghazvini, et al.
Experimental Eye Research|April 20, 2001
Spectrum of mutations in USH2A in British patients with Usher syndrome type IIB P Leroy, J A Aragon-Martin, M D Weston, et al.
Pageof 4

Showing results (21-30 of 36) with videos related to

Sort By:
Pageof 4
International Journal of Pediatric Otorhinolaryngology|November 5, 2010
Etiological diagnosis in the hearing impaired newborn: proposal of a flow chartE M R De Leenheer, S Janssens, E Padalko, et al.
Bulletin De La Societe Belge D'Ophtalmologie|June 14, 2014
Bifocal optic and facial nerve t-cell lymphomaA Van Hoey, A Shah, J De Zaeytijd, et al.
The British Journal of Radiology|February 25, 2006
Visceral and testicular calcifications as part of the phenotype in pseudoxanthoma elasticum: ultrasound findings in Belgian patients and healthy carriersO M Vanakker, D Voet, M Petrovic, et al.
Experimental Eye Research|December 21, 2005
Retinal vessel dilation following repletion of vitamin A deficiencyM Larsen, R Pedersen, N C B B Taarnhøj, et al.
Investigative Ophthalmology & Visual Science|October 29, 2000
Novel locus for autosomal recessive cone-rod dystrophy CORD8 mapping to chromosome 1q12-Q24S Khaliq, A Hameed, M Ismail, et al.
The British Journal of Ophthalmology|May 19, 2007
High beta-trace protein concentration in the fluid of an orbital cyst associated with bilateral colobomatous microphthalmosC E Decock, C M Breusegem, E H Van Aken, et al.
European Journal of Human Genetics : EJHG|January 1, 1996
Refined genetic and physical mapping of BPES type IIL Messiaen, B P Leroy, S De Bie, et al.
Clinical Genetics|April 19, 2003
The contribution of USH1C mutations to syndromic and non-syndromic deafness in the UKD C Blaydon, R F Mueller, T P Hutchin, et al.
Stem Cell Research|May 30, 2025
Generation of two iPSC lines (UGENTi003 and UGENTi004) from patients with intermediate rod-cone dystrophy carrying the c.[-123C>T;701G>A];[806_810del] variants in the RDH12 geneM Bouckaert, F Van Den Broeck, M Ghazvini, et al.
Experimental Eye Research|April 20, 2001
Spectrum of mutations in USH2A in British patients with Usher syndrome type IIB P Leroy, J A Aragon-Martin, M D Weston, et al.
Pageof 4