Search research articles
Contact Us
Filters
Showing results (301-310 of 368) with videos related to
Page
of 37
Sort By:
Mammalian Genome : Official Journal of the International Mammalian Genome Society
|
January 1, 1992
Interstitial deletions in DiGeorge syndrome detected with microclones from 22q11
A H Carey, U Claussen, H J Lüdecke, et al.
American Journal of Human Genetics
|
February 11, 1999
Molecular mechanism of angelman syndrome in two large families involves an imprinting mutation
T Ohta, K Buiting, H Kokkonen, et al.
Journal of Intellectual Disability Research : JIDR
|
May 22, 2009
The European Prader-Willi Syndrome Clinical Research Database: an aid in the investigation of a rare genetically determined neurodevelopmental disorder
A Holland, J Whittington, O Cohen, et al.
Human Molecular Genetics
|
February 9, 1999
The ancestral gene for transcribed, low-copy repeats in the Prader-Willi/Angelman region encodes a large protein implicated in protein trafficking, which is deficient in mice with neuromuscular and spermiogenic abnormalities
Y Ji, M J Walkowicz, K Buiting, et al.
American Journal of Human Genetics
|
December 1, 1999
A 28-kb deletion spanning D15S63 (PW71) in five families: a rare neutral variant?
K Buiting, B Dittrich, B Dworniczak, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
July 23, 1996
Minimal definition of the imprinting center and fixation of chromosome 15q11-q13 epigenotype by imprinting mutations
S Saitoh, K Buiting, P K Rogan, et al.
Scientific Reports
|
April 29, 2016
Real-time two- and three-dimensional imaging of monocyte motility and navigation on planar surfaces and in collagen matrices: roles of Rho
Robert Bzymek, Markus Horsthemke, Katrin Isfort, et al.
Lancet (London, England)
|
May 4, 1985
A common DNA polymorphism of the low-density lipoprotein (LDL) receptor gene and its use in diagnosis
S E Humphries, A M Kessling, B Horsthemke, et al.
European Journal of Human Genetics : EJHG
|
October 16, 2003
Novel missense mutations in the TRPS1 transcription factor define the nuclear localization signal
Frank J Kaiser, Paola Brega, Michael L Raff, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
September 1, 1990
Somatic cell hybrid and long-range physical mapping of 11p13 microdissected genomic clones
L M Davis, G Senger, H J Lüdecke, et al.
Page
of 37
Search research articles
Search
Showing results (301-310 of 368) with videos related to
Sort By:
Page
of 37
Mammalian Genome : Official Journal of the International Mammalian Genome Society
|
January 1, 1992
Interstitial deletions in DiGeorge syndrome detected with microclones from 22q11
A H Carey, U Claussen, H J Lüdecke, et al.
American Journal of Human Genetics
|
February 11, 1999
Molecular mechanism of angelman syndrome in two large families involves an imprinting mutation
T Ohta, K Buiting, H Kokkonen, et al.
Journal of Intellectual Disability Research : JIDR
|
May 22, 2009
The European Prader-Willi Syndrome Clinical Research Database: an aid in the investigation of a rare genetically determined neurodevelopmental disorder
A Holland, J Whittington, O Cohen, et al.
Human Molecular Genetics
|
February 9, 1999
The ancestral gene for transcribed, low-copy repeats in the Prader-Willi/Angelman region encodes a large protein implicated in protein trafficking, which is deficient in mice with neuromuscular and spermiogenic abnormalities
Y Ji, M J Walkowicz, K Buiting, et al.
American Journal of Human Genetics
|
December 1, 1999
A 28-kb deletion spanning D15S63 (PW71) in five families: a rare neutral variant?
K Buiting, B Dittrich, B Dworniczak, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
July 23, 1996
Minimal definition of the imprinting center and fixation of chromosome 15q11-q13 epigenotype by imprinting mutations
S Saitoh, K Buiting, P K Rogan, et al.
Scientific Reports
|
April 29, 2016
Real-time two- and three-dimensional imaging of monocyte motility and navigation on planar surfaces and in collagen matrices: roles of Rho
Robert Bzymek, Markus Horsthemke, Katrin Isfort, et al.
Lancet (London, England)
|
May 4, 1985
A common DNA polymorphism of the low-density lipoprotein (LDL) receptor gene and its use in diagnosis
S E Humphries, A M Kessling, B Horsthemke, et al.
European Journal of Human Genetics : EJHG
|
October 16, 2003
Novel missense mutations in the TRPS1 transcription factor define the nuclear localization signal
Frank J Kaiser, Paola Brega, Michael L Raff, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
September 1, 1990
Somatic cell hybrid and long-range physical mapping of 11p13 microdissected genomic clones
L M Davis, G Senger, H J Lüdecke, et al.
Page
of 37