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Clinical genetics

Showing results (501-510 of 7,173) with videos related to

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Clinical Genetics|February 6, 2004
Polymorphisms in cytokines and growth factor genes and their association with acute rejection and recurrence of hepatitis C virus disease in liver transplantationV R Mas, R A Fisher, D G Maluf, et al.
Clinical Genetics|February 6, 2004
Concordance of phenotypic expression and gender identity in a large kindred with a mutation in the androgen receptorH T Hooper, B C Figueiredo, C C Pavan-Senn, et al.
Clinical Genetics|December 1, 1977
Chylothorax in two mongoloid infantsB S Yoss, P J Lipsitz
Clinical Genetics|July 4, 2019
Clinicogenetic lessons from 370 patients with autosomal recessive limb-girdle muscular dystrophyPablo B Winckler, André M S da Silva, Antônio R Coimbra-Neto, et al.
Clinical Genetics|June 25, 2019
Novel TRRAP mutation causes autosomal dominant non-syndromic hearing lossWenjun Xia, Jiongjiong Hu, Jing Ma, et al.
Clinical Genetics|May 1, 1985
A folate sensitive heritable fragile site at 19p13N Tommerup, J Nielsen, M Mikkelsen
Clinical Genetics|October 11, 2019
Skeletal abnormalities are common features in Aymé-Gripp syndromeMarcello Niceta, Domenico Barbuti, Neerja Gupta, et al.
Clinical Genetics|October 11, 2019
Identification of a novel heterozygous guanosine monophosphate reductase (GMPR) variant in a patient with a late-onset disorder of mitochondrial DNA maintenanceEwen W Sommerville, Ilaria Dalla Rosa, Masha M Rosenberg, et al.
Clinical Genetics|February 1, 1988
Clinical findings in 12 patients with MPS IV A (Morquio's disease). Further evidence for heterogeneity. Part I: Clinical and biochemical findingsJ Nelson, D Broadhead, J Mossman
Clinical Genetics|July 12, 2019
FGF12p.Gly112Ser variant as a cause of phenytoin/phenobarbital responsive epilepsyJustyna Paprocka, Aleksandra Jezela-Stanek, Agniesz Koppolu, et al.
Pageof 718

Showing results (501-510 of 7,173) with videos related to

Sort By:
Pageof 718
Clinical Genetics|February 6, 2004
Polymorphisms in cytokines and growth factor genes and their association with acute rejection and recurrence of hepatitis C virus disease in liver transplantationV R Mas, R A Fisher, D G Maluf, et al.
Clinical Genetics|February 6, 2004
Concordance of phenotypic expression and gender identity in a large kindred with a mutation in the androgen receptorH T Hooper, B C Figueiredo, C C Pavan-Senn, et al.
Clinical Genetics|December 1, 1977
Chylothorax in two mongoloid infantsB S Yoss, P J Lipsitz
Clinical Genetics|July 4, 2019
Clinicogenetic lessons from 370 patients with autosomal recessive limb-girdle muscular dystrophyPablo B Winckler, André M S da Silva, Antônio R Coimbra-Neto, et al.
Clinical Genetics|June 25, 2019
Novel TRRAP mutation causes autosomal dominant non-syndromic hearing lossWenjun Xia, Jiongjiong Hu, Jing Ma, et al.
Clinical Genetics|May 1, 1985
A folate sensitive heritable fragile site at 19p13N Tommerup, J Nielsen, M Mikkelsen
Clinical Genetics|October 11, 2019
Skeletal abnormalities are common features in Aymé-Gripp syndromeMarcello Niceta, Domenico Barbuti, Neerja Gupta, et al.
Clinical Genetics|October 11, 2019
Identification of a novel heterozygous guanosine monophosphate reductase (GMPR) variant in a patient with a late-onset disorder of mitochondrial DNA maintenanceEwen W Sommerville, Ilaria Dalla Rosa, Masha M Rosenberg, et al.
Clinical Genetics|February 1, 1988
Clinical findings in 12 patients with MPS IV A (Morquio's disease). Further evidence for heterogeneity. Part I: Clinical and biochemical findingsJ Nelson, D Broadhead, J Mossman
Clinical Genetics|July 12, 2019
FGF12p.Gly112Ser variant as a cause of phenytoin/phenobarbital responsive epilepsyJustyna Paprocka, Aleksandra Jezela-Stanek, Agniesz Koppolu, et al.
Pageof 718