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Showing results (31-40 of 39) with videos related to

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Human Molecular Genetics|September 16, 1998
CAG repeat expansion in autosomal dominant familial spastic paraparesis: novel expansion in a subset of patientsK F Benson, M Horwitz, J Wolff, et al.
The American Journal of Medicine|January 1, 1991
Captopril renography in the diagnosis of renal artery stenosis: accuracy and limitationsS J Mann, T G Pickering, T A Sos, et al.
Prehospital Emergency Care|October 28, 2025
EMS Care of Survivors of Sexual Assault - A Position Statement and Resource Document of NAEMSPDavid H Yang, Lauren K Friend, Christie L Fritz, et al.
Lancet (London, England)|November 28, 1992
Phenotype and genotype heterogeneity in autosomal dominant polycystic kidney diseaseD Ravine, R G Walker, R N Gibson, et al.
Cytogenetic and Genome Research|April 18, 2009
A 1q44 deletion, paternal UPD of chromosome 2 and a deletion due to a complex translocation detected in children with abnormal phenotypes using new SNP array technologyB A Talseth-Palmer, N A Bowden, C Meldrum, et al.
Human Genetics|February 1, 1990
Probe, VK5B, is located in the same interval as the autosomal dominant adult polycystic kidney disease locus, PKD1V J Hyland, G K Suthers, K Friend, et al.
Molecular Psychiatry|August 10, 2011
CCDC22: a novel candidate gene for syndromic X-linked intellectual disabilityI Voineagu, L Huang, K Winden, et al.
Annals of Human Genetics|September 1, 1996
Dynamic mutation loci: allele distributions in different populationsR I Richards, J Crawford, K Narahara, et al.
American Journal of Human Genetics|June 23, 1998
Sporadic imprinting defects in Prader-Willi syndrome and Angelman syndrome: implications for imprint-switch models, genetic counseling, and prenatal diagnosisK Buiting, B Dittrich, S Gross, et al.
Pageof 4

Showing results (31-40 of 39) with videos related to

Sort By:
Pageof 4
You have reached the last page of results.This site can display upto 39 results.
Human Molecular Genetics|September 16, 1998
CAG repeat expansion in autosomal dominant familial spastic paraparesis: novel expansion in a subset of patientsK F Benson, M Horwitz, J Wolff, et al.
The American Journal of Medicine|January 1, 1991
Captopril renography in the diagnosis of renal artery stenosis: accuracy and limitationsS J Mann, T G Pickering, T A Sos, et al.
Prehospital Emergency Care|October 28, 2025
EMS Care of Survivors of Sexual Assault - A Position Statement and Resource Document of NAEMSPDavid H Yang, Lauren K Friend, Christie L Fritz, et al.
Lancet (London, England)|November 28, 1992
Phenotype and genotype heterogeneity in autosomal dominant polycystic kidney diseaseD Ravine, R G Walker, R N Gibson, et al.
Cytogenetic and Genome Research|April 18, 2009
A 1q44 deletion, paternal UPD of chromosome 2 and a deletion due to a complex translocation detected in children with abnormal phenotypes using new SNP array technologyB A Talseth-Palmer, N A Bowden, C Meldrum, et al.
Human Genetics|February 1, 1990
Probe, VK5B, is located in the same interval as the autosomal dominant adult polycystic kidney disease locus, PKD1V J Hyland, G K Suthers, K Friend, et al.
Molecular Psychiatry|August 10, 2011
CCDC22: a novel candidate gene for syndromic X-linked intellectual disabilityI Voineagu, L Huang, K Winden, et al.
Annals of Human Genetics|September 1, 1996
Dynamic mutation loci: allele distributions in different populationsR I Richards, J Crawford, K Narahara, et al.
American Journal of Human Genetics|June 23, 1998
Sporadic imprinting defects in Prader-Willi syndrome and Angelman syndrome: implications for imprint-switch models, genetic counseling, and prenatal diagnosisK Buiting, B Dittrich, S Gross, et al.
Pageof 4