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E Legius

Showing results (1-10 of 120) with videos related to

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European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|October 13, 2000
Visual loss as the presenting sign of Jeune syndromeI Casteels, E Demandt, E Legius
American Journal of Medical Genetics|March 1, 1996
Progressive extrapyramidal disorder with primary hypogonadism and alopecia in sibs: a new syndrome?K Devriendt, E Legius, J P Fryns
Journal of Medical Genetics|June 14, 2008
Clinical and molecular aspects of RAS related disordersE Denayer, Th de Ravel, E Legius
Clinical Genetics|April 1, 1994
Clinical aspects of the MASA syndrome in a large family, including expressing femalesL Kaepernick, E Legius, J Higgins, et al.
Ophthalmic Genetics|November 22, 2017
Unilateral Coats'-like disease and an intragenic deletion in the TERC gene: A case reportG Peene, E Smets, E Legius, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|March 24, 2015
Comparative study of the ophthalmological examinations in neurofibromatosis type 1. Proposal for a new screening algorithmS Caen, C Cassiman, E Legius, et al.
Genetic Counseling (Geneva, Switzerland)|January 1, 1994
Catel-Manzke palatodigital syndrome in a second trimester female foetus with nuchal oedema, costovertebral anomalies and radial ray defectP Petit, P Moerman, E Legius, et al.
Clinical Genetics|May 1, 1990
Dominant branchial cleft syndrome with characteristics of both branchio-oto-renal and branchio-oculo-facial syndromeE Legius, J P Fryns, H Van den Berghe
American Journal of Medical Genetics|August 9, 1996
Molecular-intelligence correlations in young fragile X males with a mild CGG repeat expansion in the FMR1 geneJ Steyaert, M Borghgraef, E Legius, et al.
Journal of Medical Genetics|August 1, 1989
Auralcephalosyndactyly: a new craniosynostosis syndrome or a variant of the Saethre-Chotzen syndrome?E Legius, J P Fryns, H Van den Berghe
Pageof 12

Showing results (1-10 of 120) with videos related to

Sort By:
Pageof 12
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|October 13, 2000
Visual loss as the presenting sign of Jeune syndromeI Casteels, E Demandt, E Legius
American Journal of Medical Genetics|March 1, 1996
Progressive extrapyramidal disorder with primary hypogonadism and alopecia in sibs: a new syndrome?K Devriendt, E Legius, J P Fryns
Journal of Medical Genetics|June 14, 2008
Clinical and molecular aspects of RAS related disordersE Denayer, Th de Ravel, E Legius
Clinical Genetics|April 1, 1994
Clinical aspects of the MASA syndrome in a large family, including expressing femalesL Kaepernick, E Legius, J Higgins, et al.
Ophthalmic Genetics|November 22, 2017
Unilateral Coats'-like disease and an intragenic deletion in the TERC gene: A case reportG Peene, E Smets, E Legius, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|March 24, 2015
Comparative study of the ophthalmological examinations in neurofibromatosis type 1. Proposal for a new screening algorithmS Caen, C Cassiman, E Legius, et al.
Genetic Counseling (Geneva, Switzerland)|January 1, 1994
Catel-Manzke palatodigital syndrome in a second trimester female foetus with nuchal oedema, costovertebral anomalies and radial ray defectP Petit, P Moerman, E Legius, et al.
Clinical Genetics|May 1, 1990
Dominant branchial cleft syndrome with characteristics of both branchio-oto-renal and branchio-oculo-facial syndromeE Legius, J P Fryns, H Van den Berghe
American Journal of Medical Genetics|August 9, 1996
Molecular-intelligence correlations in young fragile X males with a mild CGG repeat expansion in the FMR1 geneJ Steyaert, M Borghgraef, E Legius, et al.
Journal of Medical Genetics|August 1, 1989
Auralcephalosyndactyly: a new craniosynostosis syndrome or a variant of the Saethre-Chotzen syndrome?E Legius, J P Fryns, H Van den Berghe
Pageof 12