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Kristina Lagerstedt Robinson

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Clinical Chemistry|July 3, 2024
Atypical Interference in Hb A1c Measurements Might Be Due to Mosaic Expression of Hemoglobin VariantsAnnelie Strålfors, Kristina Lagerstedt-Robinson, Britta Landin
Journal of Human Genetics|October 24, 2009
No association between a promoter NOS1 polymorphism (rs41279104) and Infantile Hypertrophic Pyloric StenosisKristina Lagerstedt-Robinson, Anna Svenningsson, Agneta Nordenskjöld
International Journal of Endocrinology|April 21, 2012
Multigeneration Inheritance through Fertile XX Carriers of an NR0B1 (DAX1) Locus Duplication in a Kindred of Females with Isolated XY Gonadal DysgenesisMichela Barbaro, Jackie Cook, Kristina Lagerstedt-Robinson, et al.
Neurology. Genetics|September 22, 2021
Novel Mutation of the TGF-β 3 Protein (Loeys-Dietz Type 5) Associated With Aortic and Carotid Dissections: Case ReportDargham Hussein, Christian Olsson, Kristina Lagerstedt-Robinson, et al.
European Journal of Medical Genetics|August 26, 2023
Tissue specific trisomy 15 mosaicism associated with urogenital malformationsAgneta Nordenskjöld, Kristina Lagerstedt-Robinson, Britt-Marie Anderlid, et al.
Scientific Reports|July 20, 2021
Sequencing for germline mutations in Swedish breast cancer families reveals novel breast cancer risk genesHafdis T Helgadottir, Jessada Thutkawkorapin, Kristina Lagerstedt-Robinson, 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.
Scandinavian Journal of Gastroenterology|December 22, 2018
Testing strategies to reduce morbidity and mortality from Lynch syndromeAnne Keränen, Sam Ghazi, Joseph Carlson, et al.
Pediatric Surgery International|May 25, 2026
Rare variants in TTC7A, ROCK2 and LIMK2 suggest a role for the ROCK-signaling pathway in isolated intestinal malrotationKarin Salehi Karlslätt, Maria Pettersson, Kristina Lagerstedt-Robinson, et al.
Acta Ophthalmologica|June 10, 2026
Dystrophia Smolandiensis is characterized by a novel NQO1 variant and a distinct phenotype from COL17A1-associated epithelial recurrent erosion dystrophyKarl De Geer, Kristina Lagerstedt-Robinson, Daniel Nilsson, et al.
Pageof 8

Showing results (1-10 of 71) with videos related to

Sort By:
Pageof 8
Clinical Chemistry|July 3, 2024
Atypical Interference in Hb A1c Measurements Might Be Due to Mosaic Expression of Hemoglobin VariantsAnnelie Strålfors, Kristina Lagerstedt-Robinson, Britta Landin
Journal of Human Genetics|October 24, 2009
No association between a promoter NOS1 polymorphism (rs41279104) and Infantile Hypertrophic Pyloric StenosisKristina Lagerstedt-Robinson, Anna Svenningsson, Agneta Nordenskjöld
International Journal of Endocrinology|April 21, 2012
Multigeneration Inheritance through Fertile XX Carriers of an NR0B1 (DAX1) Locus Duplication in a Kindred of Females with Isolated XY Gonadal DysgenesisMichela Barbaro, Jackie Cook, Kristina Lagerstedt-Robinson, et al.
Neurology. Genetics|September 22, 2021
Novel Mutation of the TGF-β 3 Protein (Loeys-Dietz Type 5) Associated With Aortic and Carotid Dissections: Case ReportDargham Hussein, Christian Olsson, Kristina Lagerstedt-Robinson, et al.
European Journal of Medical Genetics|August 26, 2023
Tissue specific trisomy 15 mosaicism associated with urogenital malformationsAgneta Nordenskjöld, Kristina Lagerstedt-Robinson, Britt-Marie Anderlid, et al.
Scientific Reports|July 20, 2021
Sequencing for germline mutations in Swedish breast cancer families reveals novel breast cancer risk genesHafdis T Helgadottir, Jessada Thutkawkorapin, Kristina Lagerstedt-Robinson, 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.
Scandinavian Journal of Gastroenterology|December 22, 2018
Testing strategies to reduce morbidity and mortality from Lynch syndromeAnne Keränen, Sam Ghazi, Joseph Carlson, et al.
Pediatric Surgery International|May 25, 2026
Rare variants in TTC7A, ROCK2 and LIMK2 suggest a role for the ROCK-signaling pathway in isolated intestinal malrotationKarin Salehi Karlslätt, Maria Pettersson, Kristina Lagerstedt-Robinson, et al.
Acta Ophthalmologica|June 10, 2026
Dystrophia Smolandiensis is characterized by a novel NQO1 variant and a distinct phenotype from COL17A1-associated epithelial recurrent erosion dystrophyKarl De Geer, Kristina Lagerstedt-Robinson, Daniel Nilsson, et al.
Pageof 8