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Cytogenetics and Cell Genetics
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April 18, 2001
Report and abstracts of the sixth international workshop on human chromosome 1 mapping 2000. Iowa City, Iowa, USA. 30 September-3 October 2000
B C Schutte, J D Carpten, A Forus, et al.
Progress in Clinical and Biological Research
|
January 1, 1977
HLA-A9 and survival in acute lymphocytic leukemia and myelocytic leukemia
E Cohen, D P Singal, U Khurana, et al.
Cytogenetics and Cell Genetics
|
March 7, 2000
Report of the fifth international workshop on human chromosome 1 mapping 1999
P S White, A Forus, T C Matise, et al.
Human Mutation
|
October 23, 2001
Matroshka and ectopic polymorphisms: Two new classes of DNA sequence variation identified at the Van der Woude syndrome locus on 1q32-q41
Y Watanabe, J C Murray, B C Bjork, et al.
Multiple Sclerosis and Related Disorders
|
March 17, 2019
Metabolome-based signature of disease pathology in MS
S L Andersen, F B S Briggs, J H Winnike, et al.
Genomics
|
January 1, 1996
Refined mapping and YAC contig construction of the X-linked cleft palate and ankyloglossia locus (CPX) including the proximal X-Y homology breakpoint within Xq21.3
S A Forbes, L Brennan, M Richardson, et al.
Frontiers in Cell and Developmental Biology
|
June 28, 2023
Gene-nutrient interactions that impact magnesium homeostasis increase risk for neural tube defects in mice exposed to dolutegravir
J Gelineau-van Waes, M A van Waes, J Hallgren, et al.
Oncogene
|
October 16, 2007
1p36 is a preferential target of chromosome 1 deletions in astrocytic tumours and homozygously deleted in a subset of glioblastomas
K Ichimura, A P Vogazianou, L Liu, et al.
Genome Research
|
January 25, 2000
A preliminary gene map for the Van der Woude syndrome critical region derived from 900 kb of genomic sequence at 1q32-q41
B C Schutte, B C Bjork, K B Coppage, et al.
Journal of Medical Genetics
|
February 4, 2005
Tiling path resolution mapping of constitutional 1p36 deletions by array-CGH: contiguous gene deletion or "deletion with positional effect" syndrome?
R Redon, M Rio, S G Gregory, et al.
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of 4
Search research articles
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Showing results (11-20 of 31) with videos related to
Sort By:
Page
of 4
Cytogenetics and Cell Genetics
|
April 18, 2001
Report and abstracts of the sixth international workshop on human chromosome 1 mapping 2000. Iowa City, Iowa, USA. 30 September-3 October 2000
B C Schutte, J D Carpten, A Forus, et al.
Progress in Clinical and Biological Research
|
January 1, 1977
HLA-A9 and survival in acute lymphocytic leukemia and myelocytic leukemia
E Cohen, D P Singal, U Khurana, et al.
Cytogenetics and Cell Genetics
|
March 7, 2000
Report of the fifth international workshop on human chromosome 1 mapping 1999
P S White, A Forus, T C Matise, et al.
Human Mutation
|
October 23, 2001
Matroshka and ectopic polymorphisms: Two new classes of DNA sequence variation identified at the Van der Woude syndrome locus on 1q32-q41
Y Watanabe, J C Murray, B C Bjork, et al.
Multiple Sclerosis and Related Disorders
|
March 17, 2019
Metabolome-based signature of disease pathology in MS
S L Andersen, F B S Briggs, J H Winnike, et al.
Genomics
|
January 1, 1996
Refined mapping and YAC contig construction of the X-linked cleft palate and ankyloglossia locus (CPX) including the proximal X-Y homology breakpoint within Xq21.3
S A Forbes, L Brennan, M Richardson, et al.
Frontiers in Cell and Developmental Biology
|
June 28, 2023
Gene-nutrient interactions that impact magnesium homeostasis increase risk for neural tube defects in mice exposed to dolutegravir
J Gelineau-van Waes, M A van Waes, J Hallgren, et al.
Oncogene
|
October 16, 2007
1p36 is a preferential target of chromosome 1 deletions in astrocytic tumours and homozygously deleted in a subset of glioblastomas
K Ichimura, A P Vogazianou, L Liu, et al.
Genome Research
|
January 25, 2000
A preliminary gene map for the Van der Woude syndrome critical region derived from 900 kb of genomic sequence at 1q32-q41
B C Schutte, B C Bjork, K B Coppage, et al.
Journal of Medical Genetics
|
February 4, 2005
Tiling path resolution mapping of constitutional 1p36 deletions by array-CGH: contiguous gene deletion or "deletion with positional effect" syndrome?
R Redon, M Rio, S G Gregory, et al.
Page
of 4