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Nature Genetics
|
June 1, 1992
The peripheral myelin protein gene PMP-22 is contained within the Charcot-Marie-Tooth disease type 1A duplication
V Timmerman, E Nelis, W Van Hul, et al.
American Journal of Medical Genetics
|
March 3, 1997
Growth hormone deficiency associated in the 18q deletion syndrome
P D Ghidoni, D E Hale, J D Cody, et al.
American Journal of Human Genetics
|
January 1, 1989
Fine structure DNA mapping studies of the chromosomal region harboring the genetic defect in neurofibromatosis type I
P O'Connell, R J Leach, D H Ledbetter, et al.
Oncogene
|
September 27, 2006
PHC3, a component of the hPRC-H complex, associates with E2F6 during G0 and is lost in osteosarcoma tumors
A M Deshpande, J D Akunowicz, X T Reveles, et al.
Journal of Animal Science
|
June 6, 2013
The change in differing leukocyte populations during vaccination to bovine respiratory disease and their correlations with lung scores, health records, and average daily gain
R J Leach, C G Chitko-McKown, G L Bennett, et al.
Oncogene
|
July 1, 1994
Two novel human serine/threonine kinases with homologies to the cell cycle regulating Xenopus MO15, and NIMA kinases: cloning and characterization of their expression pattern
E N Levedakou, M He, E W Baptist, et al.
Molecular Psychiatry
|
April 19, 2007
TGFB-induced factor (TGIF): a candidate gene for psychosis on chromosome 18p
I Chavarría-Siles, C Walss-Bass, P Quezada, et al.
American Journal of Human Genetics
|
January 1, 1989
Physical mapping of the von Recklinghausen neurofibromatosis region on chromosome 17
J W Fountain, M R Wallace, A M Brereton, et al.
American Journal of Medical Genetics
|
June 8, 2001
Genetic mapping of a novel X-linked recessive colobomatous microphthalmia
D M Lehman, W E Sponsel, R F Stratton, et al.
Molecular Pathology : MP
|
June 5, 2003
Regions of allelic imbalance in the distal portion of chromosome 12q in gastric cancer
B G Schneider, S Y Rha, H C Chung, et al.
Page
of 8
Search research articles
Search
Showing results (61-70 of 76) with videos related to
Sort By:
Page
of 8
Nature Genetics
|
June 1, 1992
The peripheral myelin protein gene PMP-22 is contained within the Charcot-Marie-Tooth disease type 1A duplication
V Timmerman, E Nelis, W Van Hul, et al.
American Journal of Medical Genetics
|
March 3, 1997
Growth hormone deficiency associated in the 18q deletion syndrome
P D Ghidoni, D E Hale, J D Cody, et al.
American Journal of Human Genetics
|
January 1, 1989
Fine structure DNA mapping studies of the chromosomal region harboring the genetic defect in neurofibromatosis type I
P O'Connell, R J Leach, D H Ledbetter, et al.
Oncogene
|
September 27, 2006
PHC3, a component of the hPRC-H complex, associates with E2F6 during G0 and is lost in osteosarcoma tumors
A M Deshpande, J D Akunowicz, X T Reveles, et al.
Journal of Animal Science
|
June 6, 2013
The change in differing leukocyte populations during vaccination to bovine respiratory disease and their correlations with lung scores, health records, and average daily gain
R J Leach, C G Chitko-McKown, G L Bennett, et al.
Oncogene
|
July 1, 1994
Two novel human serine/threonine kinases with homologies to the cell cycle regulating Xenopus MO15, and NIMA kinases: cloning and characterization of their expression pattern
E N Levedakou, M He, E W Baptist, et al.
Molecular Psychiatry
|
April 19, 2007
TGFB-induced factor (TGIF): a candidate gene for psychosis on chromosome 18p
I Chavarría-Siles, C Walss-Bass, P Quezada, et al.
American Journal of Human Genetics
|
January 1, 1989
Physical mapping of the von Recklinghausen neurofibromatosis region on chromosome 17
J W Fountain, M R Wallace, A M Brereton, et al.
American Journal of Medical Genetics
|
June 8, 2001
Genetic mapping of a novel X-linked recessive colobomatous microphthalmia
D M Lehman, W E Sponsel, R F Stratton, et al.
Molecular Pathology : MP
|
June 5, 2003
Regions of allelic imbalance in the distal portion of chromosome 12q in gastric cancer
B G Schneider, S Y Rha, H C Chung, et al.
Page
of 8