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E Legius

Showing results (61-70 of 120) with videos related to

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Genes, Chromosomes & Cancer|January 1, 1991
Molecular and cytogenetic analysis of tumors in von Recklinghausen neurofibromatosisT W Glover, C K Stein, E Legius, et al.
Genetic Counseling (Geneva, Switzerland)|January 23, 1999
The macrocephaly-cutis marmorata telangiectatica congenita syndrome. Long-term follow-up data in 4 children and adolescentsA Vogels, K Devriendt, E Legius, et al.
Neurology|May 16, 2002
Familial temporal lobe epilepsy with febrile seizuresC Depondt, W Van Paesschen, G Matthijs, et al.
American Journal of Medical Genetics|December 1, 1990
Opitz C syndrome and pseudohypoaldosteronismJ De Koster, E Legius, F de Zegher, et al.
Journal of Medical Genetics|August 6, 2002
PTPN11 mutations in LEOPARD syndromeE Legius, C Schrander-Stumpel, E Schollen, et al.
Genetic Counseling (Geneva, Switzerland)|April 7, 1999
The behavioural phenotype in velo-cardio-facial syndrome (VCFS): from infancy to adolescenceA Swillen, K Devriendt, E Legius, et al.
Medical and Pediatric Oncology|January 1, 1995
Consecutive glioblastoma and B cell non-Hodgkin's lymphoma in a young child with von Recklinghausen's NeurofibromatosisA Uyttebroeck, E Legius, P Brock, et al.
Genetic Counseling (Geneva, Switzerland)|November 5, 1999
A novel 7.4 kb mitochondrial deletion in a patient with congenital progressive external ophthalmoplegia, muscle weakness and mental retardationM Tabaku, E Legius, W Robberecht, et al.
Genes, Chromosomes & Cancer|October 27, 1999
Germline mutations in NF1 patients with malignanciesR Wu, C López-Correa, J L Rutkowski, et al.
Journal of Medical Genetics|April 1, 1997
Prader-Willi syndrome in a child with mosaic trisomy 15 and mosaic triplo-X: a molecular analysisK Devriendt, G Matthijs, S Claes, et al.
Pageof 12

Showing results (61-70 of 120) with videos related to

Sort By:
Pageof 12
Genes, Chromosomes & Cancer|January 1, 1991
Molecular and cytogenetic analysis of tumors in von Recklinghausen neurofibromatosisT W Glover, C K Stein, E Legius, et al.
Genetic Counseling (Geneva, Switzerland)|January 23, 1999
The macrocephaly-cutis marmorata telangiectatica congenita syndrome. Long-term follow-up data in 4 children and adolescentsA Vogels, K Devriendt, E Legius, et al.
Neurology|May 16, 2002
Familial temporal lobe epilepsy with febrile seizuresC Depondt, W Van Paesschen, G Matthijs, et al.
American Journal of Medical Genetics|December 1, 1990
Opitz C syndrome and pseudohypoaldosteronismJ De Koster, E Legius, F de Zegher, et al.
Journal of Medical Genetics|August 6, 2002
PTPN11 mutations in LEOPARD syndromeE Legius, C Schrander-Stumpel, E Schollen, et al.
Genetic Counseling (Geneva, Switzerland)|April 7, 1999
The behavioural phenotype in velo-cardio-facial syndrome (VCFS): from infancy to adolescenceA Swillen, K Devriendt, E Legius, et al.
Medical and Pediatric Oncology|January 1, 1995
Consecutive glioblastoma and B cell non-Hodgkin's lymphoma in a young child with von Recklinghausen's NeurofibromatosisA Uyttebroeck, E Legius, P Brock, et al.
Genetic Counseling (Geneva, Switzerland)|November 5, 1999
A novel 7.4 kb mitochondrial deletion in a patient with congenital progressive external ophthalmoplegia, muscle weakness and mental retardationM Tabaku, E Legius, W Robberecht, et al.
Genes, Chromosomes & Cancer|October 27, 1999
Germline mutations in NF1 patients with malignanciesR Wu, C López-Correa, J L Rutkowski, et al.
Journal of Medical Genetics|April 1, 1997
Prader-Willi syndrome in a child with mosaic trisomy 15 and mosaic triplo-X: a molecular analysisK Devriendt, G Matthijs, S Claes, et al.
Pageof 12