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Ellika Sahlin

Showing results (1-10 of 16) with videos related to

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Plos One|April 30, 2015
Fetal calcifications are associated with chromosomal abnormalitiesEllika Sahlin, Meeli Sirotkina, Andreas Marnerides, et al.
American Journal of Medical Genetics. Part A|September 25, 2014
Intragenic duplication--a novel causative mechanism for SATB2-associated syndromeAgne Liedén, Malin Kvarnung, Daniel Nilssson, et al.
Hereditary Cancer in Clinical Practice|April 8, 2021
Massive parallel sequencing in a family with rectal cancerKarin Wallander, Jessada Thutkawkorapin, Ellika Sahlin, et al.
Journal of Genetic Counseling|August 3, 2016
Knowledge and Attitudes Regarding Non-Invasive Prenatal Testing (NIPT) and Preferences for Risk Information among High School Students in SwedenSusanne Georgsson, Ellika Sahlin, Moa Iwarsson, et al.
Genomics|December 28, 2014
Amplification-free sequencing of cell-free DNA for prenatal non-invasive diagnosis of chromosomal aberrationsKasper Karlsson, Ellika Sahlin, Erik Iwarsson, et al.
Plos One|May 20, 2016
Positive Attitudes towards Non-Invasive Prenatal Testing (NIPT) in a Swedish Cohort of 1,003 Pregnant WomenEllika Sahlin, Magnus Nordenskjöld, Peter Gustavsson, et al.
Fetal Diagnosis and Therapy|July 26, 2014
Molecular and cytogenetic analysis in stillbirth: results from 481 consecutive casesEllika Sahlin, Peter Gustavsson, Agne Liedén, et al.
Molecular Genetics & Genomic Medicine|December 15, 2019
Pathogenic copy number variants are detected in a subset of patients with gastrointestinal malformationsJohanna Winberg, Peter Gustavsson, Ellika Sahlin, et al.
Plos One|January 8, 2019
Identification of putative pathogenic single nucleotide variants (SNVs) in genes associated with heart disease in 290 cases of stillbirthEllika Sahlin, Anna Gréen, Peter Gustavsson, et al.
Acta Paediatrica (Oslo, Norway : 1992)|February 10, 2015
Rare copy number variants are common in young children with autism spectrum disorderMats Anders Eriksson, Agne Liedén, Joakim Westerlund, et al.
Pageof 2

Showing results (1-10 of 16) with videos related to

Sort By:
Pageof 2
Plos One|April 30, 2015
Fetal calcifications are associated with chromosomal abnormalitiesEllika Sahlin, Meeli Sirotkina, Andreas Marnerides, et al.
American Journal of Medical Genetics. Part A|September 25, 2014
Intragenic duplication--a novel causative mechanism for SATB2-associated syndromeAgne Liedén, Malin Kvarnung, Daniel Nilssson, et al.
Hereditary Cancer in Clinical Practice|April 8, 2021
Massive parallel sequencing in a family with rectal cancerKarin Wallander, Jessada Thutkawkorapin, Ellika Sahlin, et al.
Journal of Genetic Counseling|August 3, 2016
Knowledge and Attitudes Regarding Non-Invasive Prenatal Testing (NIPT) and Preferences for Risk Information among High School Students in SwedenSusanne Georgsson, Ellika Sahlin, Moa Iwarsson, et al.
Genomics|December 28, 2014
Amplification-free sequencing of cell-free DNA for prenatal non-invasive diagnosis of chromosomal aberrationsKasper Karlsson, Ellika Sahlin, Erik Iwarsson, et al.
Plos One|May 20, 2016
Positive Attitudes towards Non-Invasive Prenatal Testing (NIPT) in a Swedish Cohort of 1,003 Pregnant WomenEllika Sahlin, Magnus Nordenskjöld, Peter Gustavsson, et al.
Fetal Diagnosis and Therapy|July 26, 2014
Molecular and cytogenetic analysis in stillbirth: results from 481 consecutive casesEllika Sahlin, Peter Gustavsson, Agne Liedén, et al.
Molecular Genetics & Genomic Medicine|December 15, 2019
Pathogenic copy number variants are detected in a subset of patients with gastrointestinal malformationsJohanna Winberg, Peter Gustavsson, Ellika Sahlin, et al.
Plos One|January 8, 2019
Identification of putative pathogenic single nucleotide variants (SNVs) in genes associated with heart disease in 290 cases of stillbirthEllika Sahlin, Anna Gréen, Peter Gustavsson, et al.
Acta Paediatrica (Oslo, Norway : 1992)|February 10, 2015
Rare copy number variants are common in young children with autism spectrum disorderMats Anders Eriksson, Agne Liedén, Joakim Westerlund, et al.
Pageof 2