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S Claes

Showing results (21-30 of 44) with videos related to

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American Journal of Medical Genetics|July 9, 1999
Regional localization of a gene for nonspecific XLMR to Xp11.3-p11. 23 (MRX51) and tentative localization of an MRX gene to Xq23-q26.1S Claes, P Volcke, K Devriendt, et al.
Psychological Medicine|August 31, 2012
Self-critical perfectionism and its relationship to fatigue and pain in the daily flow of life in patients with chronic fatigue syndromeS Kempke, P Luyten, S Claes, 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.
Knee Surgery, Sports Traumatology, Arthroscopy : Official Journal of the ESSKA|February 3, 2025
Improving predictability of post-operative knee joint line obliquity in high tibial osteotomy: A new radiographic parameter correcting for foot positionM Mertens, N van Beek, T Claes, et al.
Clinical Genetics|October 23, 1997
X-linked severe mental retardation and a progressive neurological disorder in a Belgian family: clinical and genetic studiesS Claes, K Devriendt, P D'Adamo, 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.
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|September 12, 2000
Novel syndromic form of X-linked complicated spastic paraplegiaS Claes, K Devriendt, G Van Goethem, et al.
Human Mutation|February 6, 1998
Hydrocephalus and spastic paraplegia result from a donor splice site mutation (2872 + 1G to A) in the L1CAM gene in a Venezuelan pedigreeS Claes, T Aguirre, V Simosa, et al.
Annals of Neurology|October 23, 1997
The X-linked infantile spasms syndrome (MIM 308350) maps to Xp11.4-Xpter in two pedigreesS Claes, K Devriendt, L Lagae, et al.
Pageof 5

Showing results (21-30 of 44) with videos related to

Sort By:
Pageof 5
American Journal of Medical Genetics|July 9, 1999
Regional localization of a gene for nonspecific XLMR to Xp11.3-p11. 23 (MRX51) and tentative localization of an MRX gene to Xq23-q26.1S Claes, P Volcke, K Devriendt, et al.
Psychological Medicine|August 31, 2012
Self-critical perfectionism and its relationship to fatigue and pain in the daily flow of life in patients with chronic fatigue syndromeS Kempke, P Luyten, S Claes, 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.
Knee Surgery, Sports Traumatology, Arthroscopy : Official Journal of the ESSKA|February 3, 2025
Improving predictability of post-operative knee joint line obliquity in high tibial osteotomy: A new radiographic parameter correcting for foot positionM Mertens, N van Beek, T Claes, et al.
Clinical Genetics|October 23, 1997
X-linked severe mental retardation and a progressive neurological disorder in a Belgian family: clinical and genetic studiesS Claes, K Devriendt, P D'Adamo, 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.
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|September 12, 2000
Novel syndromic form of X-linked complicated spastic paraplegiaS Claes, K Devriendt, G Van Goethem, et al.
Human Mutation|February 6, 1998
Hydrocephalus and spastic paraplegia result from a donor splice site mutation (2872 + 1G to A) in the L1CAM gene in a Venezuelan pedigreeS Claes, T Aguirre, V Simosa, et al.
Annals of Neurology|October 23, 1997
The X-linked infantile spasms syndrome (MIM 308350) maps to Xp11.4-Xpter in two pedigreesS Claes, K Devriendt, L Lagae, et al.
Pageof 5