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Daniel Swan

Showing results (11-20 of 18) with videos related to

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European Journal of Human Genetics : EJHG|July 11, 2013
Autosomal dominant SCA5 and autosomal recessive infantile SCA are allelic conditions resulting from SPTBN2 mutationsSolaf M Elsayed, Raoul Heller, Michaela Thoenes, et al.
American Journal of Human Genetics|August 7, 2012
A mutation in the 5'-UTR of IFITM5 creates an in-frame start codon and causes autosomal-dominant osteogenesis imperfecta type V with hyperplastic callusOliver Semler, Lutz Garbes, Katharina Keupp, et al.
ACS Synthetic Biology|September 8, 2017
Leaf LIMS: A Flexible Laboratory Information Management System with a Synthetic Biology FocusThomas Craig, Richard Holland, Rosalinda D'Amore, et al.
Human Mutation|November 24, 2015
PEX6 is Expressed in Photoreceptor Cilia and Mutated in Deafblindness with Enamel Dysplasia and MicrocephalyMaha S Zaki, Raoul Heller, Michaela Thoenes, et al.
Genome Research|February 5, 2017
Improving and correcting the contiguity of long-read genome assemblies of three plant species using optical mapping and chromosome conformation capture dataWen-Biao Jiao, Gonzalo Garcia Accinelli, Benjamin Hartwig, et al.
BMC Genomics|November 9, 2015
Crowdsourced direct-to-consumer genomic analysis of a family quartetManuel Corpas, Willy Valdivia-Granda, Nazareth Torres, et al.
BMC Biology|October 8, 2016
Emergence of wheat blast in Bangladesh was caused by a South American lineage of Magnaporthe oryzaeM Tofazzal Islam, Daniel Croll, Pierre Gladieux, et al.
American Journal of Human Genetics|November 22, 2016
Mutations in Three Genes Encoding Proteins Involved in Hair Shaft Formation Cause Uncombable Hair SyndromeF Buket Ü Basmanav, Laura Cau, Aylar Tafazzoli, et al.
Pageof 2

Showing results (11-20 of 18) with videos related to

Sort By:
Pageof 2
You have reached the last page of results.This site can display upto 18 results.
European Journal of Human Genetics : EJHG|July 11, 2013
Autosomal dominant SCA5 and autosomal recessive infantile SCA are allelic conditions resulting from SPTBN2 mutationsSolaf M Elsayed, Raoul Heller, Michaela Thoenes, et al.
American Journal of Human Genetics|August 7, 2012
A mutation in the 5'-UTR of IFITM5 creates an in-frame start codon and causes autosomal-dominant osteogenesis imperfecta type V with hyperplastic callusOliver Semler, Lutz Garbes, Katharina Keupp, et al.
ACS Synthetic Biology|September 8, 2017
Leaf LIMS: A Flexible Laboratory Information Management System with a Synthetic Biology FocusThomas Craig, Richard Holland, Rosalinda D'Amore, et al.
Human Mutation|November 24, 2015
PEX6 is Expressed in Photoreceptor Cilia and Mutated in Deafblindness with Enamel Dysplasia and MicrocephalyMaha S Zaki, Raoul Heller, Michaela Thoenes, et al.
Genome Research|February 5, 2017
Improving and correcting the contiguity of long-read genome assemblies of three plant species using optical mapping and chromosome conformation capture dataWen-Biao Jiao, Gonzalo Garcia Accinelli, Benjamin Hartwig, et al.
BMC Genomics|November 9, 2015
Crowdsourced direct-to-consumer genomic analysis of a family quartetManuel Corpas, Willy Valdivia-Granda, Nazareth Torres, et al.
BMC Biology|October 8, 2016
Emergence of wheat blast in Bangladesh was caused by a South American lineage of Magnaporthe oryzaeM Tofazzal Islam, Daniel Croll, Pierre Gladieux, et al.
American Journal of Human Genetics|November 22, 2016
Mutations in Three Genes Encoding Proteins Involved in Hair Shaft Formation Cause Uncombable Hair SyndromeF Buket Ü Basmanav, Laura Cau, Aylar Tafazzoli, et al.
Pageof 2