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Anna Lindstrand

Showing results (101-110 of 127) with videos related to

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Cell|September 26, 2025
Intrinsic heterogeneity of primary cilia revealed through spatial proteomicsJan N Hansen, Huangqingbo Sun, Konstantin Kahnert, et al.
Basic and Clinical Andrology|November 7, 2018
Male reproductive health statement (XIIIth international symposium on Spermatology, may 9th-12th 2018, Stockholm, SwedenHagai Levine, Hideo Mohri, Anders Ekbom, et al.
Biorxiv : the Preprint Server for Biology|October 24, 2023
Break-induced replication underlies formation of inverted triplications and generates unexpected diversity in haplotype structuresChristopher M Grochowski, Jesse D Bengtsson, Haowei Du, et al.
Genome Medicine|November 8, 2019
From cytogenetics to cytogenomics: whole-genome sequencing as a first-line test comprehensively captures the diverse spectrum of disease-causing genetic variation underlying intellectual disabilityAnna Lindstrand, Jesper Eisfeldt, Maria Pettersson, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|September 6, 2022
Genome sequencing is a sensitive first-line test to diagnose individuals with intellectual disabilityAnna Lindstrand, Marlene Ek, Malin Kvarnung, et al.
Genome Research|October 29, 2024
A national long-read sequencing study on chromosomal rearrangements uncovers hidden complexitiesJesper Eisfeldt, Adam Ameur, Felix Lenner, et al.
Frontiers in Genetics|July 7, 2025
Diagnostic yield of 1000 trio analyses with exome and genome sequencing in a clinical settingHelena Malmgren, Malin Kvarnung, Peter Gustafsson, et al.
Cell Genomics|June 22, 2024
Inverted triplications formed by iterative template switches generate structural variant diversity at genomic disorder lociChristopher M Grochowski, Jesse D Bengtsson, Haowei Du, et al.
American Journal of Human Genetics|July 16, 2013
ARMC4 mutations cause primary ciliary dyskinesia with randomization of left/right body asymmetryRim Hjeij, Anna Lindstrand, Richard Francis, et al.
Journal of Medical Genetics|May 11, 2010
Further molecular and clinical delineation of co-locating 17p13.3 microdeletions and microduplications that show distinctive phenotypesDamien L Bruno, Britt-Marie Anderlid, Anna Lindstrand, et al.
Pageof 13

Showing results (101-110 of 127) with videos related to

Sort By:
Pageof 13
Cell|September 26, 2025
Intrinsic heterogeneity of primary cilia revealed through spatial proteomicsJan N Hansen, Huangqingbo Sun, Konstantin Kahnert, et al.
Basic and Clinical Andrology|November 7, 2018
Male reproductive health statement (XIIIth international symposium on Spermatology, may 9th-12th 2018, Stockholm, SwedenHagai Levine, Hideo Mohri, Anders Ekbom, et al.
Biorxiv : the Preprint Server for Biology|October 24, 2023
Break-induced replication underlies formation of inverted triplications and generates unexpected diversity in haplotype structuresChristopher M Grochowski, Jesse D Bengtsson, Haowei Du, et al.
Genome Medicine|November 8, 2019
From cytogenetics to cytogenomics: whole-genome sequencing as a first-line test comprehensively captures the diverse spectrum of disease-causing genetic variation underlying intellectual disabilityAnna Lindstrand, Jesper Eisfeldt, Maria Pettersson, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|September 6, 2022
Genome sequencing is a sensitive first-line test to diagnose individuals with intellectual disabilityAnna Lindstrand, Marlene Ek, Malin Kvarnung, et al.
Genome Research|October 29, 2024
A national long-read sequencing study on chromosomal rearrangements uncovers hidden complexitiesJesper Eisfeldt, Adam Ameur, Felix Lenner, et al.
Frontiers in Genetics|July 7, 2025
Diagnostic yield of 1000 trio analyses with exome and genome sequencing in a clinical settingHelena Malmgren, Malin Kvarnung, Peter Gustafsson, et al.
Cell Genomics|June 22, 2024
Inverted triplications formed by iterative template switches generate structural variant diversity at genomic disorder lociChristopher M Grochowski, Jesse D Bengtsson, Haowei Du, et al.
American Journal of Human Genetics|July 16, 2013
ARMC4 mutations cause primary ciliary dyskinesia with randomization of left/right body asymmetryRim Hjeij, Anna Lindstrand, Richard Francis, et al.
Journal of Medical Genetics|May 11, 2010
Further molecular and clinical delineation of co-locating 17p13.3 microdeletions and microduplications that show distinctive phenotypesDamien L Bruno, Britt-Marie Anderlid, Anna Lindstrand, et al.
Pageof 13