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T Kahre

Showing results (1-10 of 6) with videos related to

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Acta Paediatrica (Oslo, Norway : 1992)|March 27, 2010
Factor V Leiden and prothrombin 20210G>A [corrected] mutation and paediatric ischaemic stroke: a case-control study and two meta-analysesR Laugesaar, T Kahre, A Kolk, et al.
Clinical Genetics|April 6, 2017
Large gene panel sequencing in clinical diagnostics-results from 501 consecutive casesS Pajusalu, T Kahre, H Roomere, et al.
Frontiers in Genetics|January 28, 2025
Uncovering somatic mosaic variants of <i>PIK3CA</i>-related overgrowth disorders - three cases with different clinical presentationsM Tooming, P Mertsina, T Kahre, et al.
JIMD Reports|February 23, 2013
Prevalence of Long-Chain 3-Hydroxyacyl-CoA Dehydrogenase Deficiency in EstoniaK Joost, K Ounap, R Zordania, et al.
Advances in Medical Sciences|November 14, 2013
Hearing impairment in Estonia: an algorithm to investigate genetic causes in pediatric patientsR Teek, K Kruustük, R Žordania, et al.
Andrology|March 24, 2017
The number of CAG and GGN triplet repeats in the Androgen Receptor gene exert combinatorial effect on hormonal and sperm parameters in young menM Grigorova, M Punab, T Kahre, et al.
Pageof 1

Showing results (1-10 of 6) with videos related to

Sort By:
Pageof 1
Acta Paediatrica (Oslo, Norway : 1992)|March 27, 2010
Factor V Leiden and prothrombin 20210G>A [corrected] mutation and paediatric ischaemic stroke: a case-control study and two meta-analysesR Laugesaar, T Kahre, A Kolk, et al.
Clinical Genetics|April 6, 2017
Large gene panel sequencing in clinical diagnostics-results from 501 consecutive casesS Pajusalu, T Kahre, H Roomere, et al.
Frontiers in Genetics|January 28, 2025
Uncovering somatic mosaic variants of <i>PIK3CA</i>-related overgrowth disorders - three cases with different clinical presentationsM Tooming, P Mertsina, T Kahre, et al.
JIMD Reports|February 23, 2013
Prevalence of Long-Chain 3-Hydroxyacyl-CoA Dehydrogenase Deficiency in EstoniaK Joost, K Ounap, R Zordania, et al.
Advances in Medical Sciences|November 14, 2013
Hearing impairment in Estonia: an algorithm to investigate genetic causes in pediatric patientsR Teek, K Kruustük, R Žordania, et al.
Andrology|March 24, 2017
The number of CAG and GGN triplet repeats in the Androgen Receptor gene exert combinatorial effect on hormonal and sperm parameters in young menM Grigorova, M Punab, T Kahre, et al.
Pageof 1