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European Journal of Obstetrics, Gynecology, and Reproductive Biology
|
February 16, 1999
Genetic abnormalities and male infertility. A comprehensive review
B F Thielemans, C Spiessens, T D'Hooghe, et al.
Genetic Counseling (Geneva, Switzerland)
|
January 1, 1993
Oculo-auriculo-vertebral spectrum malformation and contralateral absence of internal carotid artery
E Legius, M Hellemans, G Wilms, et al.
Journal of Medical Genetics
|
November 1, 1990
MASA syndrome: new clinical features and linkage analysis using DNA probes
C Schrander-Stumpel, E Legius, J P Fryns, et al.
Genetic Counseling (Geneva, Switzerland)
|
January 1, 1996
Marden-Walker phenotype: a diagnostic dilemma
D Soekarman, P Volcke, E Legius, et al.
Documenta Ophthalmologica. Advances in Ophthalmology
|
July 26, 2013
Role of visual evoked potentials in the assessment and management of optic pathway gliomas in children
C Van Mierlo, W Spileers, E Legius, et al.
American Journal of Medical Genetics
|
August 9, 1996
New findings in the behavioral profile of young FraX females
M Borghgraef, S Umans, J Steyaert, et al.
Clinical Genetics
|
August 1, 1990
Sporadic late onset ornithine transcarbamylase deficiency in a boy with somatic mosaicism for an intragenic deletion
E Legius, E Baten, M Stul, et al.
Annales De Genetique
|
January 1, 1985
Schinzel acrocallosal syndrome: a variant example of the Greig syndrome?
E Legius, J P Fryns, P Casaer, et al.
Brain & Development
|
January 1, 1985
Intraparenchymal meningioma in a 14-month-old infant: case report
E Legius, J S Vles, P Casaer, et al.
American Journal of Medical Genetics
|
October 1, 1988
Holzgreve-Wagner-Rehder syndrome: Potter sequence associated with persistent buccopharyngeal membrane. A second observation
E Legius, P Moerman, J P Fryns, et al.
Page
of 12
Search research articles
Search
Showing results (21-30 of 120) with videos related to
Sort By:
Page
of 12
European Journal of Obstetrics, Gynecology, and Reproductive Biology
|
February 16, 1999
Genetic abnormalities and male infertility. A comprehensive review
B F Thielemans, C Spiessens, T D'Hooghe, et al.
Genetic Counseling (Geneva, Switzerland)
|
January 1, 1993
Oculo-auriculo-vertebral spectrum malformation and contralateral absence of internal carotid artery
E Legius, M Hellemans, G Wilms, et al.
Journal of Medical Genetics
|
November 1, 1990
MASA syndrome: new clinical features and linkage analysis using DNA probes
C Schrander-Stumpel, E Legius, J P Fryns, et al.
Genetic Counseling (Geneva, Switzerland)
|
January 1, 1996
Marden-Walker phenotype: a diagnostic dilemma
D Soekarman, P Volcke, E Legius, et al.
Documenta Ophthalmologica. Advances in Ophthalmology
|
July 26, 2013
Role of visual evoked potentials in the assessment and management of optic pathway gliomas in children
C Van Mierlo, W Spileers, E Legius, et al.
American Journal of Medical Genetics
|
August 9, 1996
New findings in the behavioral profile of young FraX females
M Borghgraef, S Umans, J Steyaert, et al.
Clinical Genetics
|
August 1, 1990
Sporadic late onset ornithine transcarbamylase deficiency in a boy with somatic mosaicism for an intragenic deletion
E Legius, E Baten, M Stul, et al.
Annales De Genetique
|
January 1, 1985
Schinzel acrocallosal syndrome: a variant example of the Greig syndrome?
E Legius, J P Fryns, P Casaer, et al.
Brain & Development
|
January 1, 1985
Intraparenchymal meningioma in a 14-month-old infant: case report
E Legius, J S Vles, P Casaer, et al.
American Journal of Medical Genetics
|
October 1, 1988
Holzgreve-Wagner-Rehder syndrome: Potter sequence associated with persistent buccopharyngeal membrane. A second observation
E Legius, P Moerman, J P Fryns, et al.
Page
of 12