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Genomics
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March 1, 1992
Assignment of two human alpha-1,3-galactosyltransferase gene sequences (GGTA1 and GGTA1P) to chromosomes 9q33-q34 and 12q14-q15
N L Shaper, S P Lin, D H Joziasse, et al.
Biochimica Et Biophysica Acta
|
November 22, 1995
Proton/peptide cotransporter (PEPT 2) from human kidney: functional characterization and chromosomal localization
S Ramamoorthy, W Liu, Y Y Ma, et al.
American Journal of Medical Genetics
|
March 15, 1993
Mosaic dup (9p) diagnosed by fluorescence in situ hybridization (FISH)
E M Petty, L H Gibson, W R Breg, et al.
Human Genetics
|
February 1, 1992
Cytogenetic and molecular characterization of marker chromosomes in patients with mosaic 45,X karyotypes
V Lindgren, C P Chen, C R Bryke, et al.
Clinical Genetics
|
March 1, 1995
Skipping of exon 12 as a consequence of a point mutation (1898 + 5G-->T) in the cystic fibrosis transmembrane conductance regulator gene found in a consanguineous Chinese family
J Zielenski, D Markiewicz, S P Lin, et al.
American Journal of Medical Genetics
|
May 15, 1993
Molecular and cytogenetic characterization of 9p- abnormalities
A S Teebi, L Gibson, J McGrath, et al.
Genomics
|
September 1, 1987
Ribonucleotide reductase M2 subunit sequences mapped to four different chromosomal sites in humans and mice: functional locus identified by its amplification in hydroxyurea-resistant cell lines
T L Yang-Feng, D E Barton, L Thelander, et al.
Genomics
|
August 1, 1992
Assignment of the human glycogen debrancher gene to chromosome 1p21
T L Yang-Feng, K Zheng, J Yu, et al.
Biochemical and Biophysical Research Communications
|
May 25, 1995
Assignment of the human folate transporter gene to chromosome 21q22.3 by somatic cell hybrid analysis and in situ hybridization
T L Yang-Feng, Y Y Ma, R Liang, et al.
Human Reproduction (Oxford, England)
|
April 1, 1991
Laparoscopic adnexectomy in a prepubertal Turner mosaic female with isodicentric Y
D B Seifer, C H Meyers-Seifer, G Lavy, et al.
Page
of 10
Search research articles
Search
Showing results (41-50 of 100) with videos related to
Sort By:
Page
of 10
Genomics
|
March 1, 1992
Assignment of two human alpha-1,3-galactosyltransferase gene sequences (GGTA1 and GGTA1P) to chromosomes 9q33-q34 and 12q14-q15
N L Shaper, S P Lin, D H Joziasse, et al.
Biochimica Et Biophysica Acta
|
November 22, 1995
Proton/peptide cotransporter (PEPT 2) from human kidney: functional characterization and chromosomal localization
S Ramamoorthy, W Liu, Y Y Ma, et al.
American Journal of Medical Genetics
|
March 15, 1993
Mosaic dup (9p) diagnosed by fluorescence in situ hybridization (FISH)
E M Petty, L H Gibson, W R Breg, et al.
Human Genetics
|
February 1, 1992
Cytogenetic and molecular characterization of marker chromosomes in patients with mosaic 45,X karyotypes
V Lindgren, C P Chen, C R Bryke, et al.
Clinical Genetics
|
March 1, 1995
Skipping of exon 12 as a consequence of a point mutation (1898 + 5G-->T) in the cystic fibrosis transmembrane conductance regulator gene found in a consanguineous Chinese family
J Zielenski, D Markiewicz, S P Lin, et al.
American Journal of Medical Genetics
|
May 15, 1993
Molecular and cytogenetic characterization of 9p- abnormalities
A S Teebi, L Gibson, J McGrath, et al.
Genomics
|
September 1, 1987
Ribonucleotide reductase M2 subunit sequences mapped to four different chromosomal sites in humans and mice: functional locus identified by its amplification in hydroxyurea-resistant cell lines
T L Yang-Feng, D E Barton, L Thelander, et al.
Genomics
|
August 1, 1992
Assignment of the human glycogen debrancher gene to chromosome 1p21
T L Yang-Feng, K Zheng, J Yu, et al.
Biochemical and Biophysical Research Communications
|
May 25, 1995
Assignment of the human folate transporter gene to chromosome 21q22.3 by somatic cell hybrid analysis and in situ hybridization
T L Yang-Feng, Y Y Ma, R Liang, et al.
Human Reproduction (Oxford, England)
|
April 1, 1991
Laparoscopic adnexectomy in a prepubertal Turner mosaic female with isodicentric Y
D B Seifer, C H Meyers-Seifer, G Lavy, et al.
Page
of 10