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N J Lench

Showing results (21-30 of 39) with videos related to

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Genomics|June 1, 1991
Cloning the mouse homolog of the human cystic fibrosis transmembrane conductance regulator geneF Tata, P Stanier, C Wicking, et al.
American Journal of Human Genetics|May 23, 1998
Autozygosity mapping, to chromosome 11q25, of a rare autosomal recessive syndrome causing histiocytosis, joint contractures, and sensorineural deafnessL M Moynihan, S E Bundey, D Heath, et al.
American Journal of Human Genetics|February 11, 1999
A gene for autosomal recessive symmetrical spastic cerebral palsy maps to chromosome 2q24-25D P McHale, S Mitchell, S Bundey, et al.
European Journal of Human Genetics : EJHG|June 15, 2000
A gene for ataxic cerebral palsy maps to chromosome 9p12-q12D P McHale, A P Jackson, Campbell, et al.
American Journal of Human Genetics|March 21, 2000
A third novel locus for primary autosomal recessive microcephaly maps to chromosome 9q34L Moynihan, A P Jackson, E Roberts, et al.
Archives of Oral Biology|May 1, 1996
Yeast artificial chromosome cloning and chromosomal localization of the abundant odontogenic keratocyst protein elafinP A Robinson, J P Leek, I M Carr, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society|October 1, 1995
A human ubiquitin conjugating enzyme, L-UBC, maps in the Alzheimer's disease locus on chromosome 14q24.3P A Robinson, J P Leek, J Thompson, et al.
Journal of Medical Genetics|September 9, 2000
A novel mutation in the mitochondrial tRNA(Ser(UCN)) gene in a family with non-syndromic sensorineural hearing impairmentT P Hutchin, M J Parker, I D Young, et al.
European Journal of Human Genetics : EJHG|February 15, 2001
A new locus for autosomal recessive non-syndromal sensorineural hearing impairment (DFNB27) on chromosome 2q23-q31L J Pulleyn, A P Jackson, E Roberts, et al.
Gut|March 13, 2003
Analysis of the IBD5 locus and potential gene-gene interactions in Crohn's diseaseK Negoro, D P B McGovern, Y Kinouchi, et al.
Pageof 4

Showing results (21-30 of 39) with videos related to

Sort By:
Pageof 4
Genomics|June 1, 1991
Cloning the mouse homolog of the human cystic fibrosis transmembrane conductance regulator geneF Tata, P Stanier, C Wicking, et al.
American Journal of Human Genetics|May 23, 1998
Autozygosity mapping, to chromosome 11q25, of a rare autosomal recessive syndrome causing histiocytosis, joint contractures, and sensorineural deafnessL M Moynihan, S E Bundey, D Heath, et al.
American Journal of Human Genetics|February 11, 1999
A gene for autosomal recessive symmetrical spastic cerebral palsy maps to chromosome 2q24-25D P McHale, S Mitchell, S Bundey, et al.
European Journal of Human Genetics : EJHG|June 15, 2000
A gene for ataxic cerebral palsy maps to chromosome 9p12-q12D P McHale, A P Jackson, Campbell, et al.
American Journal of Human Genetics|March 21, 2000
A third novel locus for primary autosomal recessive microcephaly maps to chromosome 9q34L Moynihan, A P Jackson, E Roberts, et al.
Archives of Oral Biology|May 1, 1996
Yeast artificial chromosome cloning and chromosomal localization of the abundant odontogenic keratocyst protein elafinP A Robinson, J P Leek, I M Carr, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society|October 1, 1995
A human ubiquitin conjugating enzyme, L-UBC, maps in the Alzheimer's disease locus on chromosome 14q24.3P A Robinson, J P Leek, J Thompson, et al.
Journal of Medical Genetics|September 9, 2000
A novel mutation in the mitochondrial tRNA(Ser(UCN)) gene in a family with non-syndromic sensorineural hearing impairmentT P Hutchin, M J Parker, I D Young, et al.
European Journal of Human Genetics : EJHG|February 15, 2001
A new locus for autosomal recessive non-syndromal sensorineural hearing impairment (DFNB27) on chromosome 2q23-q31L J Pulleyn, A P Jackson, E Roberts, et al.
Gut|March 13, 2003
Analysis of the IBD5 locus and potential gene-gene interactions in Crohn's diseaseK Negoro, D P B McGovern, Y Kinouchi, et al.
Pageof 4