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Clinical genetics

Showing results (371-380 of 7,173) with videos related to

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Clinical Genetics|May 1, 1981
The hydrolethalus syndrome: delineation of a "new", lethal malformation syndrome based on 28 patientsR Salonen, R Herva, R Norio
Clinical Genetics|September 1, 1984
Familial partial monosomy 5p and trisomy 5q; three cases due to paternal pericentric inversion 5 (p151q333)F A Beemer, H F de France, I J Rosina-Angelista, et al.
Clinical Genetics|September 1, 1984
Occurrences of methylmalonic aciduria and Hartnup disorder in the same familyV E Shih, J T Coulombe, S K Wadman, et al.
Clinical Genetics|August 31, 2021
Clinical, genetic, and histological features of centronuclear myopathy in the NetherlandsStacha F I Reumers, Corrie E Erasmus, Karlijn Bouman, et al.
Clinical Genetics|December 1, 1987
Elevated 1,25-dihydroxyvitamin D and normocalcaemia in presumed familial Williams syndromeJ Knudtzon, L Aksnes, L A Akslen, et al.
Clinical Genetics|September 7, 2021
Prevalence and clinical prediction of mitochondrial disorders in a large neuropediatric cohortAmelie T van der Ven, Jessika Johannsen, Fanny Kortüm, et al.
Clinical Genetics|August 22, 2022
Psychiatric genetic counseling for people with copy number variants associated with psychiatric conditionsEmily Morris, Angela Inglis, Jehannine Austin
Clinical Genetics|April 1, 1987
A final word on the tricho-rhino-phalangeal syndromesE M Bühler, U K Bühler, C Beutler, et al.
Clinical Genetics|May 20, 2021
Inflammatory factors, genetic variants, and predisposition for preterm birthJoana Couceiro, Irina Matos, José João Mendes, et al.
Clinical Genetics|May 17, 2021
Current and experimental therapeutics for Fabry diseaseVanessa Castelli, Cosimo Andrea Stamerra, Michele d'Angelo, et al.
Pageof 718

Showing results (371-380 of 7,173) with videos related to

Sort By:
Pageof 718
Clinical Genetics|May 1, 1981
The hydrolethalus syndrome: delineation of a "new", lethal malformation syndrome based on 28 patientsR Salonen, R Herva, R Norio
Clinical Genetics|September 1, 1984
Familial partial monosomy 5p and trisomy 5q; three cases due to paternal pericentric inversion 5 (p151q333)F A Beemer, H F de France, I J Rosina-Angelista, et al.
Clinical Genetics|September 1, 1984
Occurrences of methylmalonic aciduria and Hartnup disorder in the same familyV E Shih, J T Coulombe, S K Wadman, et al.
Clinical Genetics|August 31, 2021
Clinical, genetic, and histological features of centronuclear myopathy in the NetherlandsStacha F I Reumers, Corrie E Erasmus, Karlijn Bouman, et al.
Clinical Genetics|December 1, 1987
Elevated 1,25-dihydroxyvitamin D and normocalcaemia in presumed familial Williams syndromeJ Knudtzon, L Aksnes, L A Akslen, et al.
Clinical Genetics|September 7, 2021
Prevalence and clinical prediction of mitochondrial disorders in a large neuropediatric cohortAmelie T van der Ven, Jessika Johannsen, Fanny Kortüm, et al.
Clinical Genetics|August 22, 2022
Psychiatric genetic counseling for people with copy number variants associated with psychiatric conditionsEmily Morris, Angela Inglis, Jehannine Austin
Clinical Genetics|April 1, 1987
A final word on the tricho-rhino-phalangeal syndromesE M Bühler, U K Bühler, C Beutler, et al.
Clinical Genetics|May 20, 2021
Inflammatory factors, genetic variants, and predisposition for preterm birthJoana Couceiro, Irina Matos, José João Mendes, et al.
Clinical Genetics|May 17, 2021
Current and experimental therapeutics for Fabry diseaseVanessa Castelli, Cosimo Andrea Stamerra, Michele d'Angelo, et al.
Pageof 718