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Showing results (21-30 of 27) with videos related to

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Genomics|March 15, 2001
Axonemal beta heavy chain dynein DNAH9: cDNA sequence, genomic structure, and investigation of its role in primary ciliary dyskinesiaL Bartoloni, J L Blouin, A K Maiti, et al.
Nature Genetics|January 4, 2001
Insertion of beta-satellite repeats identifies a transmembrane protease causing both congenital and childhood onset autosomal recessive deafnessH S Scott, J Kudoh, M Wattenhofer, et al.
International Journal of Legal Medicine|January 1, 1997
Evaluation of Y-chromosomal STRs: a multicenter studyM Kayser, A Caglià, D Corach, et al.
International Journal of Legal Medicine|January 1, 1997
Chromosome Y microsatellites: population genetic and evolutionary aspectsP de Knijff, M Kayser, A Caglià, et al.
Human Genomics|June 30, 2016
Experience of a multidisciplinary task force with exome sequencing for Mendelian disordersS Fokstuen, P Makrythanasis, E Hammar, et al.
Nature Genetics|September 10, 1998
Schizophrenia susceptibility loci on chromosomes 13q32 and 8p21J L Blouin, B A Dombroski, S K Nath, et al.
Forensic Science International|April 20, 2001
Online reference database of European Y-chromosomal short tandem repeat (STR) haplotypesL Roewer, M Krawczak, S Willuweit, et al.
Pageof 3

Showing results (21-30 of 27) with videos related to

Sort By:
Pageof 3
You have reached the last page of results.This site can display upto 27 results.
Genomics|March 15, 2001
Axonemal beta heavy chain dynein DNAH9: cDNA sequence, genomic structure, and investigation of its role in primary ciliary dyskinesiaL Bartoloni, J L Blouin, A K Maiti, et al.
Nature Genetics|January 4, 2001
Insertion of beta-satellite repeats identifies a transmembrane protease causing both congenital and childhood onset autosomal recessive deafnessH S Scott, J Kudoh, M Wattenhofer, et al.
International Journal of Legal Medicine|January 1, 1997
Evaluation of Y-chromosomal STRs: a multicenter studyM Kayser, A Caglià, D Corach, et al.
International Journal of Legal Medicine|January 1, 1997
Chromosome Y microsatellites: population genetic and evolutionary aspectsP de Knijff, M Kayser, A Caglià, et al.
Human Genomics|June 30, 2016
Experience of a multidisciplinary task force with exome sequencing for Mendelian disordersS Fokstuen, P Makrythanasis, E Hammar, et al.
Nature Genetics|September 10, 1998
Schizophrenia susceptibility loci on chromosomes 13q32 and 8p21J L Blouin, B A Dombroski, S K Nath, et al.
Forensic Science International|April 20, 2001
Online reference database of European Y-chromosomal short tandem repeat (STR) haplotypesL Roewer, M Krawczak, S Willuweit, et al.
Pageof 3