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Nucleic Acids Research
|
September 12, 1988
Highly polymorphic locus D15S24 (CMW-1) maps to 15pter-q13. [HGM9 provisional no. D15S24]
D C Rich, C M Witkowski, K M Summers, et al.
Nature Communications
|
October 27, 2019
Quantifying the polygenic contribution to variable expressivity in eleven rare genetic disorders
M T Oetjens, M A Kelly, A C Sturm, et al.
American Journal of Human Genetics
|
November 1, 1985
Thymidylate synthase-deficient Chinese hamster cells: a selection system for human chromosome 18 and experimental system for the study of thymidylate synthase regulation and fragile X expression
R L Nussbaum, R M Walmsley, J G Lesko, et al.
Genomics
|
June 1, 1991
Assignment of the human small inducible cytokine A2 gene, SCYA2 (encoding JE or MCP-1), to 17q11.2-12: evolutionary relatedness of cytokines clustered at the same locus
B J Rollins, C C Morton, D H Ledbetter, et al.
Cancer Research
|
January 1, 1997
Deletion within the D17S34 locus in a primitive neuroectodermal tumor
L Haataja, C Raffel, D H Ledbetter, et al.
Human Genetics
|
January 1, 1984
Familial DiGeorge syndrome and associated partial monosomy of chromosome 22
F Greenberg, W E Crowder, V Paschall, et al.
Neurology
|
July 1, 1992
Causal heterogeneity in isolated lissencephaly
W B Dobyns, E R Elias, A C Newlin, et al.
Genome Research
|
August 1, 1996
Identification of a novel paternally expressed transcript adjacent to snRPN in the Prader-Willi syndrome critical region
Y Ning, A Roschke, S L Christian, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
November 1, 1981
In vitro translation of hypoxanthine/guanine phosphoribosyltransferase mRNA: characterization of a mouse neuroblastoma cell line that has elevated levels of hypoxanthine/guanine phosphoribosyltransferase protein
D W Melton, D S Konecki, D H Ledbetter, et al.
American Journal of Medical Genetics
|
December 30, 1996
Robertsonian (15q;15q) translocation in a child with Angelman syndrome: evidence of uniparental disomy
V Tonk, R A Schultz, S L Christian, et al.
Page
of 26
Search research articles
Search
Showing results (111-120 of 251) with videos related to
Sort By:
Page
of 26
Nucleic Acids Research
|
September 12, 1988
Highly polymorphic locus D15S24 (CMW-1) maps to 15pter-q13. [HGM9 provisional no. D15S24]
D C Rich, C M Witkowski, K M Summers, et al.
Nature Communications
|
October 27, 2019
Quantifying the polygenic contribution to variable expressivity in eleven rare genetic disorders
M T Oetjens, M A Kelly, A C Sturm, et al.
American Journal of Human Genetics
|
November 1, 1985
Thymidylate synthase-deficient Chinese hamster cells: a selection system for human chromosome 18 and experimental system for the study of thymidylate synthase regulation and fragile X expression
R L Nussbaum, R M Walmsley, J G Lesko, et al.
Genomics
|
June 1, 1991
Assignment of the human small inducible cytokine A2 gene, SCYA2 (encoding JE or MCP-1), to 17q11.2-12: evolutionary relatedness of cytokines clustered at the same locus
B J Rollins, C C Morton, D H Ledbetter, et al.
Cancer Research
|
January 1, 1997
Deletion within the D17S34 locus in a primitive neuroectodermal tumor
L Haataja, C Raffel, D H Ledbetter, et al.
Human Genetics
|
January 1, 1984
Familial DiGeorge syndrome and associated partial monosomy of chromosome 22
F Greenberg, W E Crowder, V Paschall, et al.
Neurology
|
July 1, 1992
Causal heterogeneity in isolated lissencephaly
W B Dobyns, E R Elias, A C Newlin, et al.
Genome Research
|
August 1, 1996
Identification of a novel paternally expressed transcript adjacent to snRPN in the Prader-Willi syndrome critical region
Y Ning, A Roschke, S L Christian, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
November 1, 1981
In vitro translation of hypoxanthine/guanine phosphoribosyltransferase mRNA: characterization of a mouse neuroblastoma cell line that has elevated levels of hypoxanthine/guanine phosphoribosyltransferase protein
D W Melton, D S Konecki, D H Ledbetter, et al.
American Journal of Medical Genetics
|
December 30, 1996
Robertsonian (15q;15q) translocation in a child with Angelman syndrome: evidence of uniparental disomy
V Tonk, R A Schultz, S L Christian, et al.
Page
of 26