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Clinical Genetics
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March 21, 2002
Trisomy 17p10-p12 resulting from a supernumerary marker chromosome derived from chromosome 17: molecular analysis and delineation of the phenotype
P Stankiewicz, S S Parka, S E Holder, et al.
Leukemia
|
March 9, 2011
Microarray detection of multiple recurring submicroscopic chromosomal aberrations in pediatric T-cell acute lymphoblastic leukemia
L Yu, M L Slovak, K Mannoor, et al.
American Journal of Human Genetics
|
December 1, 1999
A common breakpoint on 11q23 in carriers of the constitutional t(11;22) translocation
L Edelmann, E Spiteri, N McCain, et al.
American Journal of Human Genetics
|
August 1, 1997
A submicroscopic deletion in Xq26 associated with familial situs ambiguus
G B Ferrero, M Gebbia, G Pilia, et al.
Annals of Neurology
|
May 13, 1999
Proteolipid protein gene duplications causing Pelizaeus-Merzbacher disease: molecular mechanism and phenotypic manifestations
K Inoue, H Osaka, K Imaizumi, et al.
Genomics
|
January 1, 1995
Assignment of the gene (EPLG2) encoding a high-affinity binding protein for the receptor tyrosine kinase elk to a 200-kilobasepair region in human chromosome Xq12
F A Fletcher, K Huebner, L G Shaffer, et al.
American Journal of Human Genetics
|
January 1, 1995
The human homologue of the Drosophila melanogaster flightless-I gene (flil) maps within the Smith-Magenis microdeletion critical region in 17p11.2
K S Chen, P H Gunaratne, J D Hoheisel, et al.
American Journal of Human Genetics
|
February 11, 1999
DNA rearrangements on both homologues of chromosome 17 in a mildly delayed individual with a family history of autosomal dominant carpal tunnel syndrome
L Potocki, K S Chen, T Koeuth, et al.
Human Genetics
|
May 1, 1996
Duplication of the PMP22 gene in 17p partial trisomy patients with Charcot-Marie-Tooth type-1 neuropathy
B B Roa, F Greenberg, P Gunaratne, et al.
Clinical Immunology (Orlando, Fla.)
|
May 31, 2008
Monosomy 1p36 uncovers a role for OX40 in survival of activated CD4+ T cells
M M Suhoski, E E Perez, M L Heltzer, et al.
Page
of 14
Search research articles
Search
Showing results (111-120 of 133) with videos related to
Sort By:
Page
of 14
Clinical Genetics
|
March 21, 2002
Trisomy 17p10-p12 resulting from a supernumerary marker chromosome derived from chromosome 17: molecular analysis and delineation of the phenotype
P Stankiewicz, S S Parka, S E Holder, et al.
Leukemia
|
March 9, 2011
Microarray detection of multiple recurring submicroscopic chromosomal aberrations in pediatric T-cell acute lymphoblastic leukemia
L Yu, M L Slovak, K Mannoor, et al.
American Journal of Human Genetics
|
December 1, 1999
A common breakpoint on 11q23 in carriers of the constitutional t(11;22) translocation
L Edelmann, E Spiteri, N McCain, et al.
American Journal of Human Genetics
|
August 1, 1997
A submicroscopic deletion in Xq26 associated with familial situs ambiguus
G B Ferrero, M Gebbia, G Pilia, et al.
Annals of Neurology
|
May 13, 1999
Proteolipid protein gene duplications causing Pelizaeus-Merzbacher disease: molecular mechanism and phenotypic manifestations
K Inoue, H Osaka, K Imaizumi, et al.
Genomics
|
January 1, 1995
Assignment of the gene (EPLG2) encoding a high-affinity binding protein for the receptor tyrosine kinase elk to a 200-kilobasepair region in human chromosome Xq12
F A Fletcher, K Huebner, L G Shaffer, et al.
American Journal of Human Genetics
|
January 1, 1995
The human homologue of the Drosophila melanogaster flightless-I gene (flil) maps within the Smith-Magenis microdeletion critical region in 17p11.2
K S Chen, P H Gunaratne, J D Hoheisel, et al.
American Journal of Human Genetics
|
February 11, 1999
DNA rearrangements on both homologues of chromosome 17 in a mildly delayed individual with a family history of autosomal dominant carpal tunnel syndrome
L Potocki, K S Chen, T Koeuth, et al.
Human Genetics
|
May 1, 1996
Duplication of the PMP22 gene in 17p partial trisomy patients with Charcot-Marie-Tooth type-1 neuropathy
B B Roa, F Greenberg, P Gunaratne, et al.
Clinical Immunology (Orlando, Fla.)
|
May 31, 2008
Monosomy 1p36 uncovers a role for OX40 in survival of activated CD4+ T cells
M M Suhoski, E E Perez, M L Heltzer, et al.
Page
of 14