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E Legius

Showing results (91-100 of 120) with videos related to

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Journal of Applied Physiology (Bethesda, Md. : 1985)|June 1, 1997
Gender-specific regional changes in genetic structure of muscularity in early adolescenceR Loos, M Thomis, H H Maes, et al.
Genomics|August 1, 1992
NF1-related locus on chromosome 15E Legius, D A Marchuk, B K Hall, et al.
Human Mutation|October 26, 1999
Molecular studies in 20 submicroscopic neurofibromatosis type 1 gene deletionsC Lopez Correa, H Brems, C Lázaro, et al.
American Journal of Medical Genetics|December 18, 2001
Associated malformations and chromosomal anomalies in 42 cases of prenatally diagnosed diaphragmatic herniaI Witters, E Legius, P Moerman, et al.
Prenatal Diagnosis|December 18, 2001
Semilobar holoprosencephaly in a 46,XY female fetusI Witters, P Moerman, M Muenke, et al.
Genomics|August 1, 1996
Evidence for genetic heterogeneity in the carbohydrate-deficient glycoprotein syndrome type I (CDG1)G Matthijs, E Legius, E Schollen, et al.
Journal of Medical Genetics|April 1, 1994
Genetic heterogeneity in Rieger eye malformationE Legius, C E de Die-Smulders, F Verbraak, et al.
Clinical Genetics|October 23, 1997
A study of the cognitive and psychological profile in 16 children with congenital or juvenile myotonic dystrophyJ Steyaert, S Umans, D Willekens, et al.
American Journal of Human Genetics|March 28, 2003
Elevated risk for MPNST in NF1 microdeletion patientsT De Raedt, H Brems, P Wolkenstein, et al.
American Journal of Human Genetics|March 1, 1997
Skewed X-chromosome inactivation in female carriers of dyskeratosis congenitaK Devriendt, G Matthijs, E Legius, et al.
Pageof 12

Showing results (91-100 of 120) with videos related to

Sort By:
Pageof 12
Journal of Applied Physiology (Bethesda, Md. : 1985)|June 1, 1997
Gender-specific regional changes in genetic structure of muscularity in early adolescenceR Loos, M Thomis, H H Maes, et al.
Genomics|August 1, 1992
NF1-related locus on chromosome 15E Legius, D A Marchuk, B K Hall, et al.
Human Mutation|October 26, 1999
Molecular studies in 20 submicroscopic neurofibromatosis type 1 gene deletionsC Lopez Correa, H Brems, C Lázaro, et al.
American Journal of Medical Genetics|December 18, 2001
Associated malformations and chromosomal anomalies in 42 cases of prenatally diagnosed diaphragmatic herniaI Witters, E Legius, P Moerman, et al.
Prenatal Diagnosis|December 18, 2001
Semilobar holoprosencephaly in a 46,XY female fetusI Witters, P Moerman, M Muenke, et al.
Genomics|August 1, 1996
Evidence for genetic heterogeneity in the carbohydrate-deficient glycoprotein syndrome type I (CDG1)G Matthijs, E Legius, E Schollen, et al.
Journal of Medical Genetics|April 1, 1994
Genetic heterogeneity in Rieger eye malformationE Legius, C E de Die-Smulders, F Verbraak, et al.
Clinical Genetics|October 23, 1997
A study of the cognitive and psychological profile in 16 children with congenital or juvenile myotonic dystrophyJ Steyaert, S Umans, D Willekens, et al.
American Journal of Human Genetics|March 28, 2003
Elevated risk for MPNST in NF1 microdeletion patientsT De Raedt, H Brems, P Wolkenstein, et al.
American Journal of Human Genetics|March 1, 1997
Skewed X-chromosome inactivation in female carriers of dyskeratosis congenitaK Devriendt, G Matthijs, E Legius, et al.
Pageof 12