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Plos One
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January 14, 2014
Mutation screening and array comparative genomic hybridization using a 180K oligonucleotide array in VACTERL association
Johanna Winberg, Peter Gustavsson, Nikos Papadogiannakis, et al.
Ebiomedicine
|
July 19, 2020
Fetal HLA-G mediated immune tolerance and interferon response in preeclampsia
Satu Wedenoja, Masahito Yoshihara, Hindrek Teder, 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 disability
Anna 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 disability
Anna Lindstrand, Marlene Ek, Malin Kvarnung, et al.
Frontiers in Genetics
|
July 7, 2025
Diagnostic yield of 1000 trio analyses with exome and genome sequencing in a clinical setting
Helena Malmgren, Malin Kvarnung, Peter Gustafsson, et al.
Genome Medicine
|
March 17, 2021
Integration of whole genome sequencing into a healthcare setting: high diagnostic rates across multiple clinical entities in 3219 rare disease patients
Henrik Stranneheim, Kristina Lagerstedt-Robinson, Måns Magnusson, et al.
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of 2
Search research articles
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Showing results (11-20 of 16) with videos related to
Sort By:
Page
of 2
You have reached the last page of results.
This site can display upto 16 results.
Plos One
|
January 14, 2014
Mutation screening and array comparative genomic hybridization using a 180K oligonucleotide array in VACTERL association
Johanna Winberg, Peter Gustavsson, Nikos Papadogiannakis, et al.
Ebiomedicine
|
July 19, 2020
Fetal HLA-G mediated immune tolerance and interferon response in preeclampsia
Satu Wedenoja, Masahito Yoshihara, Hindrek Teder, 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 disability
Anna 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 disability
Anna Lindstrand, Marlene Ek, Malin Kvarnung, et al.
Frontiers in Genetics
|
July 7, 2025
Diagnostic yield of 1000 trio analyses with exome and genome sequencing in a clinical setting
Helena Malmgren, Malin Kvarnung, Peter Gustafsson, et al.
Genome Medicine
|
March 17, 2021
Integration of whole genome sequencing into a healthcare setting: high diagnostic rates across multiple clinical entities in 3219 rare disease patients
Henrik Stranneheim, Kristina Lagerstedt-Robinson, Måns Magnusson, et al.
Page
of 2