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Laboratory Investigation; a Journal of Technical Methods and Pathology
|
August 1, 1996
Adult, fetal, and polycystic kidney expression of polycystin, the polycystic kidney disease-1 gene product
D J Peters, L Spruit, R Klingel, et al.
Human Genetics
|
February 1, 1990
Probe, VK5B, is located in the same interval as the autosomal dominant adult polycystic kidney disease locus, PKD1
V J Hyland, G K Suthers, K Friend, et al.
Genes, Chromosomes & Cancer
|
July 1, 1991
Improved interpretation of complex chromosomal rearrangements by combined GTG banding and in situ suppression hybridization using chromosome-specific libraries and cosmid probes
V T Smit, J W Wessels, P Mollevanger, et al.
Clinical Genetics
|
November 13, 2010
Duchenne/Becker muscular dystrophy in the family: have potential carriers been tested at a molecular level?
A T J M Helderman-van den Enden, J C van den Bergen, M H Breuning, et al.
American Journal of Medical Genetics
|
September 13, 2000
Recurrent digital fibroma, focal dermal hypoplasia, and limb malformations
M H Breuning, A P Oranje, R A Langemeijer, et al.
Neurology
|
September 26, 2001
Cerebral microbleeds in CADASIL
S A Lesnik Oberstein, R van den Boom, M A van Buchem, et al.
Genomics
|
September 15, 1994
A large duplicated area in the polycystic kidney disease 1 (PKD1) region of chromosome 16 is prone to rearrangement
P C Harris, S Thomas, A B MacCarthy, et al.
Cytogenetics and Cell Genetics
|
January 1, 1990
Rapid detection of chromosome 16 inversion in acute nonlymphocytic leukemia, subtype M4: regional localization of the breakpoint in 16p
J G Dauwerse, T Kievits, G C Beverstock, et al.
International Journal of Cancer
|
March 3, 1995
Mechanisms of MRP over-expression in four human lung-cancer cell lines and analysis of the MRP amplicon
E W Eijdems, M De Haas, J M Coco-Martin, et al.
American Journal of Human Genetics
|
March 1, 1995
Batten disease gene, CLN3: linkage disequilibrium mapping in the Finnish population, and analysis of European haplotypes
H M Mitchison, A M O'Rawe, P E Taschner, et al.
Page
of 17
Search research articles
Search
Showing results (111-120 of 163) with videos related to
Sort By:
Page
of 17
Laboratory Investigation; a Journal of Technical Methods and Pathology
|
August 1, 1996
Adult, fetal, and polycystic kidney expression of polycystin, the polycystic kidney disease-1 gene product
D J Peters, L Spruit, R Klingel, et al.
Human Genetics
|
February 1, 1990
Probe, VK5B, is located in the same interval as the autosomal dominant adult polycystic kidney disease locus, PKD1
V J Hyland, G K Suthers, K Friend, et al.
Genes, Chromosomes & Cancer
|
July 1, 1991
Improved interpretation of complex chromosomal rearrangements by combined GTG banding and in situ suppression hybridization using chromosome-specific libraries and cosmid probes
V T Smit, J W Wessels, P Mollevanger, et al.
Clinical Genetics
|
November 13, 2010
Duchenne/Becker muscular dystrophy in the family: have potential carriers been tested at a molecular level?
A T J M Helderman-van den Enden, J C van den Bergen, M H Breuning, et al.
American Journal of Medical Genetics
|
September 13, 2000
Recurrent digital fibroma, focal dermal hypoplasia, and limb malformations
M H Breuning, A P Oranje, R A Langemeijer, et al.
Neurology
|
September 26, 2001
Cerebral microbleeds in CADASIL
S A Lesnik Oberstein, R van den Boom, M A van Buchem, et al.
Genomics
|
September 15, 1994
A large duplicated area in the polycystic kidney disease 1 (PKD1) region of chromosome 16 is prone to rearrangement
P C Harris, S Thomas, A B MacCarthy, et al.
Cytogenetics and Cell Genetics
|
January 1, 1990
Rapid detection of chromosome 16 inversion in acute nonlymphocytic leukemia, subtype M4: regional localization of the breakpoint in 16p
J G Dauwerse, T Kievits, G C Beverstock, et al.
International Journal of Cancer
|
March 3, 1995
Mechanisms of MRP over-expression in four human lung-cancer cell lines and analysis of the MRP amplicon
E W Eijdems, M De Haas, J M Coco-Martin, et al.
American Journal of Human Genetics
|
March 1, 1995
Batten disease gene, CLN3: linkage disequilibrium mapping in the Finnish population, and analysis of European haplotypes
H M Mitchison, A M O'Rawe, P E Taschner, et al.
Page
of 17