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Clinical genetics

Showing results (551-560 of 7,173) with videos related to

Pageof 718
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Clinical Genetics|July 1, 1985
Genetic counseling and genetic heterogeneity in the thalassemiasE Paglietti, R Galanello, M Addis, et al.
Clinical Genetics|July 4, 2018
Aldehyde dehydrogenase 2 polymorphism affects the outcome of methanol poisoning in exposed humansJ A Hubacek, M Jirsa, M Bobak, et al.
Clinical Genetics|October 4, 2018
Complex effects of laminopathy mutations on nuclear structure and functionRosettia Ho, Robert A Hegele
Clinical Genetics|May 17, 2019
The choice not to undergo genetic testing for Huntington disease: Results from the PHAROS studyKaren E Anderson, Shirley Eberly, Karen S Marder, et al.
Clinical Genetics|April 1, 1987
Albinism, or the NOACH syndrome (the book of Enoch c.v. 1-20)D B van Dorp
Clinical Genetics|May 18, 2019
Epithelial ovarian cancer risk: A review of the current genetic landscapeNicola Flaum, Emma J Crosbie, Richard J Edmondson, et al.
Clinical Genetics|April 18, 2019
Trends in phenotype in the English paediatric neurofibromatosis type 2 cohort stratified by genetic severityDorothy Halliday, Beatrice Emmanouil, Grace Vassallo, et al.
Clinical Genetics|May 16, 2019
Delineation of MidXq28-duplication syndrome distal to MECP2 and proximal to RAB39B genesLorenzo Sinibaldi, Valentina Parisi, Silvia Lanciotti, et al.
Clinical Genetics|October 10, 2018
MPV17 mutations in juvenile- and adult-onset axonal sensorimotor polyneuropathyMatthias Baumann, Herbert Schreiber, Beate Schlotter-Weigel, et al.
Clinical Genetics|August 1, 1986
Prenatal diagnosis and pathoanatomy of iniencephalyI Mórocz, G T Szeifert, P Molnár, et al.
Pageof 718

Showing results (551-560 of 7,173) with videos related to

Sort By:
Pageof 718
Clinical Genetics|July 1, 1985
Genetic counseling and genetic heterogeneity in the thalassemiasE Paglietti, R Galanello, M Addis, et al.
Clinical Genetics|July 4, 2018
Aldehyde dehydrogenase 2 polymorphism affects the outcome of methanol poisoning in exposed humansJ A Hubacek, M Jirsa, M Bobak, et al.
Clinical Genetics|October 4, 2018
Complex effects of laminopathy mutations on nuclear structure and functionRosettia Ho, Robert A Hegele
Clinical Genetics|May 17, 2019
The choice not to undergo genetic testing for Huntington disease: Results from the PHAROS studyKaren E Anderson, Shirley Eberly, Karen S Marder, et al.
Clinical Genetics|April 1, 1987
Albinism, or the NOACH syndrome (the book of Enoch c.v. 1-20)D B van Dorp
Clinical Genetics|May 18, 2019
Epithelial ovarian cancer risk: A review of the current genetic landscapeNicola Flaum, Emma J Crosbie, Richard J Edmondson, et al.
Clinical Genetics|April 18, 2019
Trends in phenotype in the English paediatric neurofibromatosis type 2 cohort stratified by genetic severityDorothy Halliday, Beatrice Emmanouil, Grace Vassallo, et al.
Clinical Genetics|May 16, 2019
Delineation of MidXq28-duplication syndrome distal to MECP2 and proximal to RAB39B genesLorenzo Sinibaldi, Valentina Parisi, Silvia Lanciotti, et al.
Clinical Genetics|October 10, 2018
MPV17 mutations in juvenile- and adult-onset axonal sensorimotor polyneuropathyMatthias Baumann, Herbert Schreiber, Beate Schlotter-Weigel, et al.
Clinical Genetics|August 1, 1986
Prenatal diagnosis and pathoanatomy of iniencephalyI Mórocz, G T Szeifert, P Molnár, et al.
Pageof 718