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Pedro Cruz

Showing results (121-130 of 126) with videos related to

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Plos Genetics|October 25, 2011
Whole-exome sequencing identifies homozygous AFG3L2 mutations in a spastic ataxia-neuropathy syndrome linked to mitochondrial m-AAA proteasesTyler Mark Pierson, David Adams, Florian Bonn, et al.
Genome Research|July 16, 2009
The ClinSeq Project: piloting large-scale genome sequencing for research in genomic medicineLeslie G Biesecker, James C Mullikin, Flavia M Facio, et al.
Plos Genetics|September 9, 2011
Predisposition to cancer caused by genetic and functional defects of mammalian Atad5Daphne W Bell, Nilabja Sikdar, Kyoo-Young Lee, et al.
Blood|August 17, 2010
Gray platelet syndrome: natural history of a large patient cohort and locus assignment to chromosome 3pMeral Gunay-Aygun, Yifat Zivony-Elboum, Fatma Gumruk, et al.
Nature Genetics|January 25, 2011
TTC21B contributes both causal and modifying alleles across the ciliopathy spectrumErica E Davis, Qi Zhang, Qin Liu, et al.
American Journal of Human Genetics|December 30, 2019
Allelic Heterogeneity at the CRP Locus Identified by Whole-Genome Sequencing in Multi-ancestry CohortsLaura M Raffield, Apoorva K Iyengar, Biqi Wang, et al.
Pageof 13

Showing results (121-130 of 126) with videos related to

Sort By:
Pageof 13
You have reached the last page of results.This site can display upto 126 results.
Plos Genetics|October 25, 2011
Whole-exome sequencing identifies homozygous AFG3L2 mutations in a spastic ataxia-neuropathy syndrome linked to mitochondrial m-AAA proteasesTyler Mark Pierson, David Adams, Florian Bonn, et al.
Genome Research|July 16, 2009
The ClinSeq Project: piloting large-scale genome sequencing for research in genomic medicineLeslie G Biesecker, James C Mullikin, Flavia M Facio, et al.
Plos Genetics|September 9, 2011
Predisposition to cancer caused by genetic and functional defects of mammalian Atad5Daphne W Bell, Nilabja Sikdar, Kyoo-Young Lee, et al.
Blood|August 17, 2010
Gray platelet syndrome: natural history of a large patient cohort and locus assignment to chromosome 3pMeral Gunay-Aygun, Yifat Zivony-Elboum, Fatma Gumruk, et al.
Nature Genetics|January 25, 2011
TTC21B contributes both causal and modifying alleles across the ciliopathy spectrumErica E Davis, Qi Zhang, Qin Liu, et al.
American Journal of Human Genetics|December 30, 2019
Allelic Heterogeneity at the CRP Locus Identified by Whole-Genome Sequencing in Multi-ancestry CohortsLaura M Raffield, Apoorva K Iyengar, Biqi Wang, et al.
Pageof 13