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American Journal of Medical Genetics
|
July 1, 1987
Waardenburg syndrome, Hirschsprung megacolon, and Marcus Gunn ptosis
F Meire, L Standaert, J J De Laey, et al.
Clinical Genetics
|
May 1, 1994
DNA carrier detection in X-linked progressive cone dystrophy
A A Bergen, F Meire, E J Schuurman, et al.
Ophthalmologica. Journal International D'Ophtalmologie. International Journal of Ophthalmology. Zeitschrift Fur Augenheilkunde
|
January 1, 1995
Unilateral cytomegalovirus retinitis in a patient with immunoglobulin G2 deficiency
B A Lafaut, R N Vianna, F De Baets, et al.
Bulletin De La Societe Belge D'Ophtalmologie
|
January 1, 1985
A study of Usher's syndrome (cases from Belgium and China)
L H Zeng, F Meire, J J De Laey, et al.
Ophthalmic Paediatrics and Genetics
|
September 1, 1990
The Hermansky-Pudlak syndrome. Variable reaction to 1-desamino-8D-arginine vasopressin for correction of the bleeding time
D B Van Dorp, P W Wijermans, F Meire, et al.
Clinical Otolaryngology and Allied Sciences
|
April 1, 1997
The endoscopic approach for congenital nasolacrimal duct obstruction
K Ingels, P Kestelyn, F Meire, et al.
Journal of Neurology
|
September 19, 2000
Mitochondrial mutations of Leber's hereditary optic neuropathy: a risk factor for multiple sclerosis
L Vanopdenbosch, B Dubois, M B D'Hooghe, et al.
Bulletin De La Societe Belge D'Ophtalmologie
|
January 1, 1992
Leber's hereditary optic neuropathy: clinical and molecular genetic aspects. Preliminary results in our families
E Van Caelenberghe, F Meire, C Broux, et al.
American Journal of Medical Genetics
|
January 1, 1993
Osteoporosis-pseudoglioma syndrome
A De Paepe, J G Leroy, L Nuytinck, et al.
Bulletin De La Societe Belge D'Ophtalmologie
|
January 1, 1995
Ocular perforation in utero
A Gobert, G Vereecken, F Meire, et al.
Page
of 6
Search research articles
Search
Showing results (21-30 of 54) with videos related to
Sort By:
Page
of 6
American Journal of Medical Genetics
|
July 1, 1987
Waardenburg syndrome, Hirschsprung megacolon, and Marcus Gunn ptosis
F Meire, L Standaert, J J De Laey, et al.
Clinical Genetics
|
May 1, 1994
DNA carrier detection in X-linked progressive cone dystrophy
A A Bergen, F Meire, E J Schuurman, et al.
Ophthalmologica. Journal International D'Ophtalmologie. International Journal of Ophthalmology. Zeitschrift Fur Augenheilkunde
|
January 1, 1995
Unilateral cytomegalovirus retinitis in a patient with immunoglobulin G2 deficiency
B A Lafaut, R N Vianna, F De Baets, et al.
Bulletin De La Societe Belge D'Ophtalmologie
|
January 1, 1985
A study of Usher's syndrome (cases from Belgium and China)
L H Zeng, F Meire, J J De Laey, et al.
Ophthalmic Paediatrics and Genetics
|
September 1, 1990
The Hermansky-Pudlak syndrome. Variable reaction to 1-desamino-8D-arginine vasopressin for correction of the bleeding time
D B Van Dorp, P W Wijermans, F Meire, et al.
Clinical Otolaryngology and Allied Sciences
|
April 1, 1997
The endoscopic approach for congenital nasolacrimal duct obstruction
K Ingels, P Kestelyn, F Meire, et al.
Journal of Neurology
|
September 19, 2000
Mitochondrial mutations of Leber's hereditary optic neuropathy: a risk factor for multiple sclerosis
L Vanopdenbosch, B Dubois, M B D'Hooghe, et al.
Bulletin De La Societe Belge D'Ophtalmologie
|
January 1, 1992
Leber's hereditary optic neuropathy: clinical and molecular genetic aspects. Preliminary results in our families
E Van Caelenberghe, F Meire, C Broux, et al.
American Journal of Medical Genetics
|
January 1, 1993
Osteoporosis-pseudoglioma syndrome
A De Paepe, J G Leroy, L Nuytinck, et al.
Bulletin De La Societe Belge D'Ophtalmologie
|
January 1, 1995
Ocular perforation in utero
A Gobert, G Vereecken, F Meire, et al.
Page
of 6