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N J Lench

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

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Nature|April 6, 1987
A candidate for the cystic fibrosis locus isolated by selection for methylation-free islandsX Estivill, M Farrall, P J Scambler, et al.
European Journal of Human Genetics : EJHG|November 26, 1999
The second locus for autosomal recessive primary microcephaly (MCPH2) maps to chromosome 19q13.1-13.2E Roberts, A P Jackson, A C Carradice, et al.
Journal of Medical Genetics|March 21, 1998
A Moroccan family with autosomal recessive sensorineural hearing loss caused by a mutation in the gap junction protein gene connexin 26 (GJB2)N J Lench, A F Markham, R F Mueller, et al.
International Journal of Pediatric Otorhinolaryngology|December 22, 1999
Congenital non-syndromal sensorineural hearing impairment due to connexin 26 gene mutations--molecular and audiological findingsR F Mueller, A Nehammer, A Middleton, et al.
American Journal of Human Genetics|November 21, 2000
Extent and distribution of linkage disequilibrium in three genomic regionsG R Abecasis, E Noguchi, A Heinzmann, et al.
American Journal of Human Genetics|July 31, 1998
Primary autosomal recessive microcephaly (MCPH1) maps to chromosome 8p22-pterA P Jackson, D P McHale, D A Campbell, et al.
Journal of Medical Genetics|January 16, 1998
A new locus for non-syndromal, autosomal recessive, sensorineural hearing loss (DFNB16) maps to human chromosome 15q21-q22D A Campbell, D P McHale, K A Brown, et al.
Human Mutation|May 26, 1998
Identification of mutations in the connexin 26 gene that cause autosomal recessive nonsyndromic hearing lossD A Scott, M L Kraft, R Carmi, et al.
Human Molecular Genetics|October 23, 1997
Prelingual deafness: high prevalence of a 30delG mutation in the connexin 26 geneF Denoyelle, D Weil, M A Maw, 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.
Nature|April 6, 1987
A candidate for the cystic fibrosis locus isolated by selection for methylation-free islandsX Estivill, M Farrall, P J Scambler, et al.
European Journal of Human Genetics : EJHG|November 26, 1999
The second locus for autosomal recessive primary microcephaly (MCPH2) maps to chromosome 19q13.1-13.2E Roberts, A P Jackson, A C Carradice, et al.
Journal of Medical Genetics|March 21, 1998
A Moroccan family with autosomal recessive sensorineural hearing loss caused by a mutation in the gap junction protein gene connexin 26 (GJB2)N J Lench, A F Markham, R F Mueller, et al.
International Journal of Pediatric Otorhinolaryngology|December 22, 1999
Congenital non-syndromal sensorineural hearing impairment due to connexin 26 gene mutations--molecular and audiological findingsR F Mueller, A Nehammer, A Middleton, et al.
American Journal of Human Genetics|November 21, 2000
Extent and distribution of linkage disequilibrium in three genomic regionsG R Abecasis, E Noguchi, A Heinzmann, et al.
American Journal of Human Genetics|July 31, 1998
Primary autosomal recessive microcephaly (MCPH1) maps to chromosome 8p22-pterA P Jackson, D P McHale, D A Campbell, et al.
Journal of Medical Genetics|January 16, 1998
A new locus for non-syndromal, autosomal recessive, sensorineural hearing loss (DFNB16) maps to human chromosome 15q21-q22D A Campbell, D P McHale, K A Brown, et al.
Human Mutation|May 26, 1998
Identification of mutations in the connexin 26 gene that cause autosomal recessive nonsyndromic hearing lossD A Scott, M L Kraft, R Carmi, et al.
Human Molecular Genetics|October 23, 1997
Prelingual deafness: high prevalence of a 30delG mutation in the connexin 26 geneF Denoyelle, D Weil, M A Maw, et al.
Pageof 4