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L Van Maldergem

Showing results (21-30 of 114) with videos related to

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Genetic Counseling (Geneva, Switzerland)|February 26, 2013
Arterial tortuosity syndrome: case reportC Karakurt, G Koçak, O Elkiran, et al.
Annales De Genetique|January 1, 1989
Roberts-SC phocomelia syndrome with exencephalyA Verloes, C Herens, L Van Maldergem, et al.
Bulletin De La Societe Belge D'Ophtalmologie|January 1, 1993
[Ophthalmological manifestations of infantile Refsum's disease: apropos of 3 cases]V Van der Maren, M Cordonnier, L Van Maldergem, et al.
Obstetrics and Gynecology|March 1, 1990
Nonimmune hydrops fetalis associated with genetic abnormalitiesE Jauniaux, L Van Maldergem, C De Munter, et al.
Clinical Genetics|June 1, 1994
Congenital cutis laxa with ligamentous laxity and delayed development, Dandy-Walker malformation and minor heart and osseous defectsA Biver, S De Rijcke, V Toppet, et al.
Journal of Inherited Metabolic Disease|August 11, 2004
Relief of gastrointestinal symptoms under enzyme replacement therapy [corrected] in patients with Fabry diseaseF Dehout, D Roland, S Treille de Granseigne, et al.
Genetic Counseling (Geneva, Switzerland)|January 1, 1991
Ring chromosome 9 in a newborn male presenting with facial dysmorphia, hypospadias and skeletal abnormalitiesL Van Maldergem, F Avni, B Mossay, et al.
Acta Paediatrica Scandinavica|March 1, 1989
Echovirus meningoencephalitis in X-linked hypogammaglobulinemiaL Van Maldergem, F Mascart, D Ureel, et al.
Journal of Medical Genetics|July 1, 1990
Microspherophakia-metaphyseal dysplasia: a 'new' dominantly inherited bone dysplasia with severe eye involvementA Verloes, L Van Maldergem, P de Marneffe, et al.
Neuropediatrics|June 1, 2000
Atypical features in Angelman syndrome due to imprinting defect of uniparental disomy of chromosome 15B Dan, S G Boyd, F Christiaens, et al.
Pageof 12

Showing results (21-30 of 114) with videos related to

Sort By:
Pageof 12
Genetic Counseling (Geneva, Switzerland)|February 26, 2013
Arterial tortuosity syndrome: case reportC Karakurt, G Koçak, O Elkiran, et al.
Annales De Genetique|January 1, 1989
Roberts-SC phocomelia syndrome with exencephalyA Verloes, C Herens, L Van Maldergem, et al.
Bulletin De La Societe Belge D'Ophtalmologie|January 1, 1993
[Ophthalmological manifestations of infantile Refsum's disease: apropos of 3 cases]V Van der Maren, M Cordonnier, L Van Maldergem, et al.
Obstetrics and Gynecology|March 1, 1990
Nonimmune hydrops fetalis associated with genetic abnormalitiesE Jauniaux, L Van Maldergem, C De Munter, et al.
Clinical Genetics|June 1, 1994
Congenital cutis laxa with ligamentous laxity and delayed development, Dandy-Walker malformation and minor heart and osseous defectsA Biver, S De Rijcke, V Toppet, et al.
Journal of Inherited Metabolic Disease|August 11, 2004
Relief of gastrointestinal symptoms under enzyme replacement therapy [corrected] in patients with Fabry diseaseF Dehout, D Roland, S Treille de Granseigne, et al.
Genetic Counseling (Geneva, Switzerland)|January 1, 1991
Ring chromosome 9 in a newborn male presenting with facial dysmorphia, hypospadias and skeletal abnormalitiesL Van Maldergem, F Avni, B Mossay, et al.
Acta Paediatrica Scandinavica|March 1, 1989
Echovirus meningoencephalitis in X-linked hypogammaglobulinemiaL Van Maldergem, F Mascart, D Ureel, et al.
Journal of Medical Genetics|July 1, 1990
Microspherophakia-metaphyseal dysplasia: a 'new' dominantly inherited bone dysplasia with severe eye involvementA Verloes, L Van Maldergem, P de Marneffe, et al.
Neuropediatrics|June 1, 2000
Atypical features in Angelman syndrome due to imprinting defect of uniparental disomy of chromosome 15B Dan, S G Boyd, F Christiaens, et al.
Pageof 12