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E Legius

Showing results (81-90 of 120) with videos related to

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Journal of Neurology, Neurosurgery, and Psychiatry|December 1, 1995
Neurofibromatosis type 1 in childhood: correlation of MRI findings with intelligenceE Legius, M J Descheemaeker, J Steyaert, et al.
Clinical Genetics|April 5, 2014
Hypotrichosis-lymphedema-telangiectasia-renal defect associated with a truncating mutation in the SOX18 geneS Moalem, P Brouillard, D Kuypers, et al.
Archives of Neurology|August 1, 1995
Correlations between triplet repeat expansion and clinical features in Huntington's diseaseS Claes, K Van Zand, E Legius, et al.
Familial Cancer|June 1, 2006
Germline mutations of the hMLH1 and hMSH2 mismatch repair genes in Belgian hereditary nonpolyposis colon cancer (HNPCC) patientsM Spaepen, B Vankeirsbilck, S Van Opstal, et al.
Journal of Medical Genetics|June 1, 1996
Unusual molecular findings in autosomal recessive spinal muscular atrophyG Matthijs, E Schollen, E Legius, et al.
Human Reproduction (Oxford, England)|March 13, 2009
Preimplantation genetic diagnosis using fluorescent in situ hybridization for cancer predisposition syndromes caused by microdeletionsE Vanneste, C Melotte, S Debrock, et al.
American Journal of Medical Genetics|April 1, 1990
Alagille syndrome (arteriohepatic dysplasia) and del(20)(p11.2)E Legius, J P Fryns, B Eyskens, et al.
American Journal of Medical Genetics|July 12, 1996
Linkage analysis in three families with nonspecific X-linked mental retardationS Claes, X X Gu, E Legius, et al.
American Journal of Medical Genetics. Part A|May 20, 2004
Psychotic disorders in Prader-Willi syndromeA Vogels, M De Hert, M J Descheemaeker, et al.
Clinical Genetics|May 1, 1995
Increased and decreased relative risk for non-insulin-dependent diabetes mellitus conferred by HLA class II and by CD4 allelesM Z Ghabanbasani, M Spaepen, I Buyse, et al.
Pageof 12

Showing results (81-90 of 120) with videos related to

Sort By:
Pageof 12
Journal of Neurology, Neurosurgery, and Psychiatry|December 1, 1995
Neurofibromatosis type 1 in childhood: correlation of MRI findings with intelligenceE Legius, M J Descheemaeker, J Steyaert, et al.
Clinical Genetics|April 5, 2014
Hypotrichosis-lymphedema-telangiectasia-renal defect associated with a truncating mutation in the SOX18 geneS Moalem, P Brouillard, D Kuypers, et al.
Archives of Neurology|August 1, 1995
Correlations between triplet repeat expansion and clinical features in Huntington's diseaseS Claes, K Van Zand, E Legius, et al.
Familial Cancer|June 1, 2006
Germline mutations of the hMLH1 and hMSH2 mismatch repair genes in Belgian hereditary nonpolyposis colon cancer (HNPCC) patientsM Spaepen, B Vankeirsbilck, S Van Opstal, et al.
Journal of Medical Genetics|June 1, 1996
Unusual molecular findings in autosomal recessive spinal muscular atrophyG Matthijs, E Schollen, E Legius, et al.
Human Reproduction (Oxford, England)|March 13, 2009
Preimplantation genetic diagnosis using fluorescent in situ hybridization for cancer predisposition syndromes caused by microdeletionsE Vanneste, C Melotte, S Debrock, et al.
American Journal of Medical Genetics|April 1, 1990
Alagille syndrome (arteriohepatic dysplasia) and del(20)(p11.2)E Legius, J P Fryns, B Eyskens, et al.
American Journal of Medical Genetics|July 12, 1996
Linkage analysis in three families with nonspecific X-linked mental retardationS Claes, X X Gu, E Legius, et al.
American Journal of Medical Genetics. Part A|May 20, 2004
Psychotic disorders in Prader-Willi syndromeA Vogels, M De Hert, M J Descheemaeker, et al.
Clinical Genetics|May 1, 1995
Increased and decreased relative risk for non-insulin-dependent diabetes mellitus conferred by HLA class II and by CD4 allelesM Z Ghabanbasani, M Spaepen, I Buyse, et al.
Pageof 12