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E Legius

Showing results (11-20 of 120) with videos related to

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European Journal of Human Genetics : EJHG|October 22, 1998
Fine mapping of Noonan/cardio-facio cutaneous syndrome in a large familyE Legius, E Schollen, G Matthijs, et al.
B-ENT|July 28, 2005
Pneumosinus dilatans and orbital meningioma in neurofibromatosis type 2T Vauterin, I Mombaerts, M Jorissen, et al.
Clinical Genetics|April 1, 1994
Fine mapping of X-linked clasped thumb and mental retardation (MASA syndrome) in Xq28E Legius, L Kaepernick, J V Higgins, et al.
Clinical Genetics|September 1, 1993
Progressive pseudorheumatoid arthritis of childhood (PPAC) and normal adult heightE Legius, M Mulier, B Van Damme, et al.
Journal of Intellectual Disability Research : JIDR|October 26, 2012
Neuropsychological profile in adults with neurofibromatosis type 1 compared to a control groupM-J Descheemaeker, E Plasschaert, J-P Frijns, et al.
Pediatric Nephrology (Berlin, Germany)|April 1, 1989
Cutaneous telangiectasia, sparse hair and membranoproliferative glomerulonephritis. A new case of a newly recognized entityW Proesmans, E Legius, K Van Herck, et al.
Genetic Counseling (Geneva, Switzerland)|January 1, 1993
The Larsen syndrome. The diagnostic contribution of the analysis of the metacarpophalangeal pattern profileL De Smet, E Legius, G Fabry, et al.
European Journal of Human Genetics : EJHG|June 15, 2000
Lack of Hardy-Weinberg equilibrium for the most prevalent PMM2 mutation in CDG-Ia (congenital disorders of glycosylation type Ia)E Schollen, S Kjaergaard, E Legius, et al.
American Journal of Human Genetics|April 25, 2000
Unequal meiotic crossover: a frequent cause of NF1 microdeletionsC López Correa, H Brems, C Lázaro, et al.
Nature Genetics|February 1, 1993
Somatic deletion of the neurofibromatosis type 1 gene in a neurofibrosarcoma supports a tumour suppressor gene hypothesisE Legius, D A Marchuk, F S Collins, et al.
Pageof 12

Showing results (11-20 of 120) with videos related to

Sort By:
Pageof 12
European Journal of Human Genetics : EJHG|October 22, 1998
Fine mapping of Noonan/cardio-facio cutaneous syndrome in a large familyE Legius, E Schollen, G Matthijs, et al.
B-ENT|July 28, 2005
Pneumosinus dilatans and orbital meningioma in neurofibromatosis type 2T Vauterin, I Mombaerts, M Jorissen, et al.
Clinical Genetics|April 1, 1994
Fine mapping of X-linked clasped thumb and mental retardation (MASA syndrome) in Xq28E Legius, L Kaepernick, J V Higgins, et al.
Clinical Genetics|September 1, 1993
Progressive pseudorheumatoid arthritis of childhood (PPAC) and normal adult heightE Legius, M Mulier, B Van Damme, et al.
Journal of Intellectual Disability Research : JIDR|October 26, 2012
Neuropsychological profile in adults with neurofibromatosis type 1 compared to a control groupM-J Descheemaeker, E Plasschaert, J-P Frijns, et al.
Pediatric Nephrology (Berlin, Germany)|April 1, 1989
Cutaneous telangiectasia, sparse hair and membranoproliferative glomerulonephritis. A new case of a newly recognized entityW Proesmans, E Legius, K Van Herck, et al.
Genetic Counseling (Geneva, Switzerland)|January 1, 1993
The Larsen syndrome. The diagnostic contribution of the analysis of the metacarpophalangeal pattern profileL De Smet, E Legius, G Fabry, et al.
European Journal of Human Genetics : EJHG|June 15, 2000
Lack of Hardy-Weinberg equilibrium for the most prevalent PMM2 mutation in CDG-Ia (congenital disorders of glycosylation type Ia)E Schollen, S Kjaergaard, E Legius, et al.
American Journal of Human Genetics|April 25, 2000
Unequal meiotic crossover: a frequent cause of NF1 microdeletionsC López Correa, H Brems, C Lázaro, et al.
Nature Genetics|February 1, 1993
Somatic deletion of the neurofibromatosis type 1 gene in a neurofibrosarcoma supports a tumour suppressor gene hypothesisE Legius, D A Marchuk, F S Collins, et al.
Pageof 12