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A 39 kb structural variant causing Lynch Syndrome detected by optical genome mapping and nanopore sequencing
by
Bjørnstad, Pål Marius
,
Aaløkken, Ragnhild
,
Åsheim, June
,
Sundaram, Arvind Y M
,
Felde, Caroline N
,
Østby, G Henriette
,
Dalland, Marianne
,
Sjursen, Wenche
,
Carrizosa, Christian
,
Vigeland, Magnus D
,
Sorte, Hanne S
,
Sheng, Ying
,
Ariansen, Sarah L
,
Grindedal, Eli Marie
,
Gilfillan, Gregor D
Published in
European journal of human genetics : EJHG
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Publisher Correction: A 39 kb structural variant causing Lynch syndrome detected by optical genome mapping and nanopore sequencing
by
Bjørnstad, Pål Marius
,
Aaløkken, Ragnhild
,
Åsheim, June
,
Sundaram, Arvind Y M
,
Felde, Caroline N
,
Østby, G Henriette
,
Dalland, Marianne
,
Sjursen, Wenche
,
Carrizosa, Christian
,
Vigeland, Magnus D
,
Sorte, Hanne S
,
Sheng, Ying
,
Ariansen, Sarah L
,
Grindedal, Eli Marie
,
Gilfillan, Gregor D
Published in
European journal of human genetics : EJHG
Get full text
Article
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European Journal Of Human Genetics : Ejhg
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Biochemistry & Molecular Biology
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Autosomal Dominant Inheritance
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Colorectal Neoplasms, Hereditary Nonpolyposis - Diagnosis
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