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H Malmgren

Showing results (31-40 of 43) with videos related to

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American Journal of Human Genetics|June 1, 1993
Linkage mapping of a severe X-linked mental retardation syndromeH Malmgren, M Sundvall, N Dahl, et al.
Clinical Genetics|October 30, 2009
Detailed molecular and clinical characterization of three patients with 21q deletionsA Lindstrand, H Malmgren, S Sahlén, et al.
American Journal of Human Genetics|August 1, 1989
Linkage analysis of families with fragile-X mental retardation, using a novel RFLP marker (DXS 304)N Dahl, P Goonewardena, H Malmgren, et al.
Dementia and Geriatric Cognitive Disorders|February 5, 2011
High white matter lesion load is associated with hippocampal atrophy in mild cognitive impairmentC Eckerström, E Olsson, N Klasson, et al.
Journal of the Neurological Sciences|June 24, 2008
Small baseline volume of left hippocampus is associated with subsequent conversion of MCI into dementia: the Göteborg MCI studyC Eckerström, E Olsson, M Borga, et al.
American Journal of Human Genetics|August 1, 1994
A multicenter study on genotype-phenotype correlations in the fragile X syndrome, using direct diagnosis with probe StB12.3: the first 2,253 casesF Rousseau, D Heitz, J Tarleton, et al.
Molecular Human Reproduction|May 8, 2002
Single cell CGH analysis reveals a high degree of mosaicism in human embryos from patients with balanced structural chromosome aberrationsH Malmgren, S Sahlén, J Inzunza, et al.
Prenatal Diagnosis|September 18, 2001
Clinical outcome of treatment cycles using preimplantation genetic diagnosis for structural chromosomal abnormalitiesM Fridström, L Ahrlund-Richter, E Iwarsson, et al.
Prenatal Diagnosis|February 17, 2001
Highly abnormal cleavage divisions in preimplantation embryos from translocation carriersE Iwarsson, H Malmgren, J Inzunza, et al.
American Journal of Medical Genetics|April 1, 1992
Methylation and mutation patterns in the fragile X syndromeH Malmgren, M L Steén-Bondeson, K H Gustavson, et al.
Pageof 5

Showing results (31-40 of 43) with videos related to

Sort By:
Pageof 5
American Journal of Human Genetics|June 1, 1993
Linkage mapping of a severe X-linked mental retardation syndromeH Malmgren, M Sundvall, N Dahl, et al.
Clinical Genetics|October 30, 2009
Detailed molecular and clinical characterization of three patients with 21q deletionsA Lindstrand, H Malmgren, S Sahlén, et al.
American Journal of Human Genetics|August 1, 1989
Linkage analysis of families with fragile-X mental retardation, using a novel RFLP marker (DXS 304)N Dahl, P Goonewardena, H Malmgren, et al.
Dementia and Geriatric Cognitive Disorders|February 5, 2011
High white matter lesion load is associated with hippocampal atrophy in mild cognitive impairmentC Eckerström, E Olsson, N Klasson, et al.
Journal of the Neurological Sciences|June 24, 2008
Small baseline volume of left hippocampus is associated with subsequent conversion of MCI into dementia: the Göteborg MCI studyC Eckerström, E Olsson, M Borga, et al.
American Journal of Human Genetics|August 1, 1994
A multicenter study on genotype-phenotype correlations in the fragile X syndrome, using direct diagnosis with probe StB12.3: the first 2,253 casesF Rousseau, D Heitz, J Tarleton, et al.
Molecular Human Reproduction|May 8, 2002
Single cell CGH analysis reveals a high degree of mosaicism in human embryos from patients with balanced structural chromosome aberrationsH Malmgren, S Sahlén, J Inzunza, et al.
Prenatal Diagnosis|September 18, 2001
Clinical outcome of treatment cycles using preimplantation genetic diagnosis for structural chromosomal abnormalitiesM Fridström, L Ahrlund-Richter, E Iwarsson, et al.
Prenatal Diagnosis|February 17, 2001
Highly abnormal cleavage divisions in preimplantation embryos from translocation carriersE Iwarsson, H Malmgren, J Inzunza, et al.
American Journal of Medical Genetics|April 1, 1992
Methylation and mutation patterns in the fragile X syndromeH Malmgren, M L Steén-Bondeson, K H Gustavson, et al.
Pageof 5