Search research articles
Contact Us
Filters
Showing results (31-40 of 42) with videos related to
Page
of 5
Sort By:
Genomics
|
May 1, 1997
Molecular cloning of the interleukin-1 gene cluster: construction of an integrated YAC/PAC contig and a partial transcriptional map in the region of chromosome 2q13
H G Nothwang, B Strahm, D Denich, et al.
Journal of Medical Genetics
|
May 5, 1999
Systematic characterisation of disease associated balanced chromosome rearrangements by FISH: cytogenetically and genetically anchored YACs identify microdeletions and candidate regions for mental retardation genes
J Wirth, H G Nothwang, S van der Maarel, et al.
Human Molecular Genetics
|
February 13, 2001
A translocation breakpoint cluster disrupts the newly defined 3' end of the SNURF-SNRPN transcription unit on chromosome 15
J Wirth, E Back, A Hüttenhofer, et al.
Nature Genetics
|
January 4, 2001
Mutation of CDH23, encoding a new member of the cadherin gene family, causes Usher syndrome type 1D
H Bolz, B von Brederlow, A Ramírez, et al.
Cytogenetics and Cell Genetics
|
November 4, 2000
Molecular cloning of Xp11 breakpoints in two unrelated mentally retarded females with X;autosome translocations
H G Nothwang, A Schröer, S van der Maarel, et al.
Human Molecular Genetics
|
April 4, 2001
Functional hemizygosity of PAFAH1B3 due to a PAFAH1B3-CLK2 fusion gene in a female with mental retardation, ataxia and atrophy of the brain
H G Nothwang, H G Kim, J Aoki, et al.
Frontiers in Molecular Neuroscience
|
August 17, 2013
L-type CaV1.2 deletion in the cochlea but not in the brainstem reduces noise vulnerability: implication for CaV1.2-mediated control of cochlear BDNF expression
Annalisa Zuccotti, Sze C Lee, Dario Campanelli, et al.
Nature Genetics
|
October 4, 2000
Mutations in ARHGEF6, encoding a guanine nucleotide exchange factor for Rho GTPases, in patients with X-linked mental retardation
K Kutsche, H Yntema, A Brandt, et al.
Cytogenetics and Cell Genetics
|
January 1, 1996
Report and abstracts of the Fourth International Workshop on Human Chromosome 2 Mapping 1996
N K Spur, R Bashir, K Bushby, et al.
Science Advances
|
June 19, 2024
Genetic identification of medullary neurons underlying congenital hypoventilation
Ke Cui, Yiling Xia, Abhisarika Patnaik, et al.
Page
of 5
Search research articles
Search
Showing results (31-40 of 42) with videos related to
Sort By:
Page
of 5
Genomics
|
May 1, 1997
Molecular cloning of the interleukin-1 gene cluster: construction of an integrated YAC/PAC contig and a partial transcriptional map in the region of chromosome 2q13
H G Nothwang, B Strahm, D Denich, et al.
Journal of Medical Genetics
|
May 5, 1999
Systematic characterisation of disease associated balanced chromosome rearrangements by FISH: cytogenetically and genetically anchored YACs identify microdeletions and candidate regions for mental retardation genes
J Wirth, H G Nothwang, S van der Maarel, et al.
Human Molecular Genetics
|
February 13, 2001
A translocation breakpoint cluster disrupts the newly defined 3' end of the SNURF-SNRPN transcription unit on chromosome 15
J Wirth, E Back, A Hüttenhofer, et al.
Nature Genetics
|
January 4, 2001
Mutation of CDH23, encoding a new member of the cadherin gene family, causes Usher syndrome type 1D
H Bolz, B von Brederlow, A Ramírez, et al.
Cytogenetics and Cell Genetics
|
November 4, 2000
Molecular cloning of Xp11 breakpoints in two unrelated mentally retarded females with X;autosome translocations
H G Nothwang, A Schröer, S van der Maarel, et al.
Human Molecular Genetics
|
April 4, 2001
Functional hemizygosity of PAFAH1B3 due to a PAFAH1B3-CLK2 fusion gene in a female with mental retardation, ataxia and atrophy of the brain
H G Nothwang, H G Kim, J Aoki, et al.
Frontiers in Molecular Neuroscience
|
August 17, 2013
L-type CaV1.2 deletion in the cochlea but not in the brainstem reduces noise vulnerability: implication for CaV1.2-mediated control of cochlear BDNF expression
Annalisa Zuccotti, Sze C Lee, Dario Campanelli, et al.
Nature Genetics
|
October 4, 2000
Mutations in ARHGEF6, encoding a guanine nucleotide exchange factor for Rho GTPases, in patients with X-linked mental retardation
K Kutsche, H Yntema, A Brandt, et al.
Cytogenetics and Cell Genetics
|
January 1, 1996
Report and abstracts of the Fourth International Workshop on Human Chromosome 2 Mapping 1996
N K Spur, R Bashir, K Bushby, et al.
Science Advances
|
June 19, 2024
Genetic identification of medullary neurons underlying congenital hypoventilation
Ke Cui, Yiling Xia, Abhisarika Patnaik, et al.
Page
of 5