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Prenatal Diagnosis
|
January 1, 1993
Fetal blood sampling and cytogenetic abnormalities
J D Liou, C P Chen, W R Breg, et al.
Human Molecular Genetics
|
December 1, 1992
Molecular isolation and characterization of an expressed gene from the human Y chromosome
J S Zhang, T L Yang-Feng, U Muller, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
September 1, 1988
Cloning and expression of a human kidney cDNA for an alpha 2-adrenergic receptor subtype
J W Regan, T S Kobilka, T L Yang-Feng, et al.
Mutagenesis
|
January 1, 1996
Frequent spontaneous deletions at a shuttle vector locus in transgenic mice
E G Leach, E J Gunther, T M Yeasky, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
January 1, 1990
C-terminal truncation of the retinoblastoma gene product leads to functional inactivation
J Y Shew, B T Lin, P L Chen, et al.
International Journal of Obesity (2005)
|
March 7, 2012
Ethnic differentiation of copy number variation on chromosome 16p12.3 for association with obesity phenotypes in European and Chinese populations
T-L Yang, Y Guo, S M Li, et al.
Prenatal Diagnosis
|
February 1, 1996
Prenatal detection of two different monosomic cell lines by chorionic villus sampling
T Y Hsu, J D Liou, J A Copel, et al.
Physical Review Letters
|
September 22, 2018
Measurement of the Dynamical Structure Factor of a 1D Interacting Fermi Gas
T L Yang, P Grišins, Y T Chang, et al.
American Journal of Medical Genetics
|
May 16, 1997
Cytogenetic and molecular studies of a familial paracentric inversion of Y chromosome present in a patient with ambiguous genitalia
J D Liou, Y Y Ma, L H Gibson, et al.
Science (New York, N.Y.)
|
August 22, 1986
Multiple, distinct forms of bovine and human protein kinase C suggest diversity in cellular signaling pathways
L Coussens, P J Parker, L Rhee, et al.
Page
of 18
Search research articles
Search
Showing results (101-110 of 178) with videos related to
Sort By:
Page
of 18
Prenatal Diagnosis
|
January 1, 1993
Fetal blood sampling and cytogenetic abnormalities
J D Liou, C P Chen, W R Breg, et al.
Human Molecular Genetics
|
December 1, 1992
Molecular isolation and characterization of an expressed gene from the human Y chromosome
J S Zhang, T L Yang-Feng, U Muller, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
September 1, 1988
Cloning and expression of a human kidney cDNA for an alpha 2-adrenergic receptor subtype
J W Regan, T S Kobilka, T L Yang-Feng, et al.
Mutagenesis
|
January 1, 1996
Frequent spontaneous deletions at a shuttle vector locus in transgenic mice
E G Leach, E J Gunther, T M Yeasky, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
January 1, 1990
C-terminal truncation of the retinoblastoma gene product leads to functional inactivation
J Y Shew, B T Lin, P L Chen, et al.
International Journal of Obesity (2005)
|
March 7, 2012
Ethnic differentiation of copy number variation on chromosome 16p12.3 for association with obesity phenotypes in European and Chinese populations
T-L Yang, Y Guo, S M Li, et al.
Prenatal Diagnosis
|
February 1, 1996
Prenatal detection of two different monosomic cell lines by chorionic villus sampling
T Y Hsu, J D Liou, J A Copel, et al.
Physical Review Letters
|
September 22, 2018
Measurement of the Dynamical Structure Factor of a 1D Interacting Fermi Gas
T L Yang, P Grišins, Y T Chang, et al.
American Journal of Medical Genetics
|
May 16, 1997
Cytogenetic and molecular studies of a familial paracentric inversion of Y chromosome present in a patient with ambiguous genitalia
J D Liou, Y Y Ma, L H Gibson, et al.
Science (New York, N.Y.)
|
August 22, 1986
Multiple, distinct forms of bovine and human protein kinase C suggest diversity in cellular signaling pathways
L Coussens, P J Parker, L Rhee, et al.
Page
of 18