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BMC Genomics
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November 11, 2005
Genetic mapping of putative Chrna7 and Luzp2 neuronal transcriptional enhancers due to impact of a transgene-insertion and 6.8 Mb deletion in a mouse model of Prader-Willi and Angelman syndromes
Mihaela Stefan, Kathryn C Claiborn, Edyta Stasiek, et al.
Journal of Medical Genetics
|
May 15, 1998
The mechanisms involved in formation of deletions and duplications of 15q11-q13
W P Robinson, F Dutly, R D Nicholls, et al.
Molecular Biology and Evolution
|
October 19, 2001
The gene orders on human chromosome 15 and chicken chromosome 10 reveal multiple inter- and intrachromosomal rearrangements
R P Crooijmans, R J Dijkhof, T Veenendaal, et al.
Nucleic Acids Research
|
November 11, 1999
Concerted regulation and molecular evolution of the duplicated SNRPB'/B and SNRPN loci
T A Gray, M J Smithwick, M A Schaldach, et al.
Gene
|
December 8, 1993
The human TYRO3 gene and pseudogene are located in chromosome 15q14-q25
A Polvi, E Armstrong, C Lai, et al.
Genomics
|
August 1, 1992
A DNA methylation imprint, determined by the sex of the parent, distinguishes the Angelman and Prader-Willi syndromes
D J Driscoll, M F Waters, C A Williams, et al.
American Journal of Medical Genetics
|
April 1, 1993
Angelman and Prader-Willi syndrome: a magnetic resonance imaging study of differences in cerebral structure
C M Leonard, C A Williams, R D Nicholls, et al.
American Journal of Medical Genetics
|
June 13, 1997
Unexpected familial recurrence in Angelman syndrome
K J Connerton-Moyer, R D Nicholls, S Schwartz, et al.
American Journal of Medical Genetics
|
October 1, 1993
Difference in methylation patterns within the D15S9 region of chromosome 15q11-13 in first cousins with Angelman syndrome and Prader-Willi syndrome
J Clayton-Smith, D J Driscoll, M F Waters, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society
|
August 12, 1999
Molecular characterization of radiation- and chemically induced mutations associated with neuromuscular tremors, runting, juvenile lethality, and sperm defects in jdf2 mice
M Walkowicz, Y Ji, X Ren, et al.
Page
of 23
Search research articles
Search
Showing results (171-180 of 228) with videos related to
Sort By:
Page
of 23
BMC Genomics
|
November 11, 2005
Genetic mapping of putative Chrna7 and Luzp2 neuronal transcriptional enhancers due to impact of a transgene-insertion and 6.8 Mb deletion in a mouse model of Prader-Willi and Angelman syndromes
Mihaela Stefan, Kathryn C Claiborn, Edyta Stasiek, et al.
Journal of Medical Genetics
|
May 15, 1998
The mechanisms involved in formation of deletions and duplications of 15q11-q13
W P Robinson, F Dutly, R D Nicholls, et al.
Molecular Biology and Evolution
|
October 19, 2001
The gene orders on human chromosome 15 and chicken chromosome 10 reveal multiple inter- and intrachromosomal rearrangements
R P Crooijmans, R J Dijkhof, T Veenendaal, et al.
Nucleic Acids Research
|
November 11, 1999
Concerted regulation and molecular evolution of the duplicated SNRPB'/B and SNRPN loci
T A Gray, M J Smithwick, M A Schaldach, et al.
Gene
|
December 8, 1993
The human TYRO3 gene and pseudogene are located in chromosome 15q14-q25
A Polvi, E Armstrong, C Lai, et al.
Genomics
|
August 1, 1992
A DNA methylation imprint, determined by the sex of the parent, distinguishes the Angelman and Prader-Willi syndromes
D J Driscoll, M F Waters, C A Williams, et al.
American Journal of Medical Genetics
|
April 1, 1993
Angelman and Prader-Willi syndrome: a magnetic resonance imaging study of differences in cerebral structure
C M Leonard, C A Williams, R D Nicholls, et al.
American Journal of Medical Genetics
|
June 13, 1997
Unexpected familial recurrence in Angelman syndrome
K J Connerton-Moyer, R D Nicholls, S Schwartz, et al.
American Journal of Medical Genetics
|
October 1, 1993
Difference in methylation patterns within the D15S9 region of chromosome 15q11-13 in first cousins with Angelman syndrome and Prader-Willi syndrome
J Clayton-Smith, D J Driscoll, M F Waters, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society
|
August 12, 1999
Molecular characterization of radiation- and chemically induced mutations associated with neuromuscular tremors, runting, juvenile lethality, and sperm defects in jdf2 mice
M Walkowicz, Y Ji, X Ren, et al.
Page
of 23