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Clinical genetics

Showing results (51-60 of 9,192) with videos related to

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Clinical Genetics|November 4, 2015
Risk assessment of medically assisted reproduction and advanced maternal ages in the development of Prader-Willi syndrome due to UPD(15)matK Matsubara, N Murakami, M Fukami, et al.
Clinical Genetics|June 11, 2016
Expanding non-invasive prenatal testing beyond chromosomes 21, 18, 13, X and YP Benn
Clinical Genetics|May 7, 2016
Whole gene duplication of SCN2A and SCN3A is associated with neonatal seizures and a normal intellectual developmentA-C Thuresson, G Van Buggenhout, F Sheth, et al.
Clinical Genetics|August 19, 2015
Utility of whole-exome sequencing for those near the end of the diagnostic odyssey: time to address gaps in careS L Sawyer, T Hartley, D A Dyment, et al.
Clinical Genetics|August 19, 2015
Sclerosteosis caused by a novel nonsense mutation of SOST in a consanguineous familyWen-Tao He, Chen Chen, Chu Pan, et al.
Clinical Genetics|April 23, 2016
Autosomal recessive mutations in THOC6 cause intellectual disability: syndrome delineation requiring forward and reverse phenotypingJ S Amos, L Huang, J Thevenon, et al.
Clinical Genetics|April 23, 2016
A novel mutation in NDUFB11 unveils a new clinical phenotype associated with lactic acidosis and sideroblastic anemiaA Torraco, M Bianchi, D Verrigni, et al.
Clinical Genetics|April 23, 2016
Social anxiety and autism spectrum traits among adult FMR1 premutation carriersO López-Mourelo, E Mur, I Madrigal, et al.
Clinical Genetics|April 1, 1989
Non-mosaic trisomy 20 in amniotic fluid cultures with minor anomalies in the fetusT L Myers, L A Prouty
Clinical Genetics|April 1, 1989
Brachydactyly type A-7 (Smorgasbord): a new entityS A Meiselman, M Berkenstadt, T Ben-Ami, et al.
Pageof 920

Showing results (51-60 of 9,192) with videos related to

Sort By:
Pageof 920
Clinical Genetics|November 4, 2015
Risk assessment of medically assisted reproduction and advanced maternal ages in the development of Prader-Willi syndrome due to UPD(15)matK Matsubara, N Murakami, M Fukami, et al.
Clinical Genetics|June 11, 2016
Expanding non-invasive prenatal testing beyond chromosomes 21, 18, 13, X and YP Benn
Clinical Genetics|May 7, 2016
Whole gene duplication of SCN2A and SCN3A is associated with neonatal seizures and a normal intellectual developmentA-C Thuresson, G Van Buggenhout, F Sheth, et al.
Clinical Genetics|August 19, 2015
Utility of whole-exome sequencing for those near the end of the diagnostic odyssey: time to address gaps in careS L Sawyer, T Hartley, D A Dyment, et al.
Clinical Genetics|August 19, 2015
Sclerosteosis caused by a novel nonsense mutation of SOST in a consanguineous familyWen-Tao He, Chen Chen, Chu Pan, et al.
Clinical Genetics|April 23, 2016
Autosomal recessive mutations in THOC6 cause intellectual disability: syndrome delineation requiring forward and reverse phenotypingJ S Amos, L Huang, J Thevenon, et al.
Clinical Genetics|April 23, 2016
A novel mutation in NDUFB11 unveils a new clinical phenotype associated with lactic acidosis and sideroblastic anemiaA Torraco, M Bianchi, D Verrigni, et al.
Clinical Genetics|April 23, 2016
Social anxiety and autism spectrum traits among adult FMR1 premutation carriersO López-Mourelo, E Mur, I Madrigal, et al.
Clinical Genetics|April 1, 1989
Non-mosaic trisomy 20 in amniotic fluid cultures with minor anomalies in the fetusT L Myers, L A Prouty
Clinical Genetics|April 1, 1989
Brachydactyly type A-7 (Smorgasbord): a new entityS A Meiselman, M Berkenstadt, T Ben-Ami, et al.
Pageof 920