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H Malmgren

Showing results (21-30 of 43) with videos related to

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American Journal of Medical Genetics|February 1, 1991
Carrier detection of the fragile X syndrome using flanking loci DXS98, DXS105, and DXS304N Dahl, H Malmgren, U Pettersson, et al.
European Journal of Human Genetics : EJHG|January 1, 1994
Strong founder effect for the fragile X syndrome in SwedenH Malmgren, K H Gustavson, C Oudet, et al.
Science (New York, N.Y.)|September 30, 1994
Padlock probes: circularizing oligonucleotides for localized DNA detectionM Nilsson, H Malmgren, M Samiotaki, et al.
Molecular Human Reproduction|April 13, 2006
PGD for dystrophin gene deletions using fluorescence in situ hybridizationH Malmgren, I White, S Johansson, et al.
American Journal of Medical Genetics|March 1, 1993
New X-linked syndrome with severe mental retardation, severely impaired vision, severe hearing defect, epileptic seizures, spasticity, restricted joint mobility, and early deathK H Gustavson, G Annerén, H Malmgren, et al.
Genomics|November 1, 1989
The polymorphic marker DXS304 is within 5 centimorgans of the fragile X locusA Vincent, N Dahl, I Oberlé, et al.
American Journal of Medical Genetics|December 1, 1992
Infantile autism--fragile X: molecular findings support genetic heterogeneityH Malmgren, K H Gustavson, J Wahlström, et al.
Human Molecular Genetics|April 1, 1995
Inversion of the IDS gene resulting from recombination with IDS-related sequences is a common cause of the Hunter syndromeM L Bondeson, N Dahl, H Malmgren, et al.
Molecular Human Reproduction|March 27, 2004
Comparative genomic hybridization and karyotyping of human embryonic stem cells reveals the occurrence of an isodicentric X chromosome after long-term cultivationJ Inzunza, S Sahlén, K Holmberg, et al.
Dementia and Geriatric Cognitive Disorders|April 15, 2010
Combination of hippocampal volume and cerebrospinal fluid biomarkers improves predictive value in mild cognitive impairmentC Eckerström, U Andreasson, E Olsson, et al.
Pageof 5

Showing results (21-30 of 43) with videos related to

Sort By:
Pageof 5
American Journal of Medical Genetics|February 1, 1991
Carrier detection of the fragile X syndrome using flanking loci DXS98, DXS105, and DXS304N Dahl, H Malmgren, U Pettersson, et al.
European Journal of Human Genetics : EJHG|January 1, 1994
Strong founder effect for the fragile X syndrome in SwedenH Malmgren, K H Gustavson, C Oudet, et al.
Science (New York, N.Y.)|September 30, 1994
Padlock probes: circularizing oligonucleotides for localized DNA detectionM Nilsson, H Malmgren, M Samiotaki, et al.
Molecular Human Reproduction|April 13, 2006
PGD for dystrophin gene deletions using fluorescence in situ hybridizationH Malmgren, I White, S Johansson, et al.
American Journal of Medical Genetics|March 1, 1993
New X-linked syndrome with severe mental retardation, severely impaired vision, severe hearing defect, epileptic seizures, spasticity, restricted joint mobility, and early deathK H Gustavson, G Annerén, H Malmgren, et al.
Genomics|November 1, 1989
The polymorphic marker DXS304 is within 5 centimorgans of the fragile X locusA Vincent, N Dahl, I Oberlé, et al.
American Journal of Medical Genetics|December 1, 1992
Infantile autism--fragile X: molecular findings support genetic heterogeneityH Malmgren, K H Gustavson, J Wahlström, et al.
Human Molecular Genetics|April 1, 1995
Inversion of the IDS gene resulting from recombination with IDS-related sequences is a common cause of the Hunter syndromeM L Bondeson, N Dahl, H Malmgren, et al.
Molecular Human Reproduction|March 27, 2004
Comparative genomic hybridization and karyotyping of human embryonic stem cells reveals the occurrence of an isodicentric X chromosome after long-term cultivationJ Inzunza, S Sahlén, K Holmberg, et al.
Dementia and Geriatric Cognitive Disorders|April 15, 2010
Combination of hippocampal volume and cerebrospinal fluid biomarkers improves predictive value in mild cognitive impairmentC Eckerström, U Andreasson, E Olsson, et al.
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