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Human Genetics
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July 1, 1993
Rapid detection of trisomy 21 by quantitative PCR
F von Eggeling, M Freytag, R Fahsold, et al.
Verhandlungen Der Deutschen Gesellschaft Fur Innere Medizin
|
January 1, 1986
DNA deletions and DNA polymorphisms of the low density lipoprotein (LDL) receptor gene--their use in diagnosis
S E Humphries, A Dunning, R Taylor, et al.
Human Molecular Genetics
|
August 1, 1993
A BanII RFLP in the ZNF34 zinc finger gene on chromosome 8
B La Pillo, H J Lüdecke, H J Thiesen, et al.
Human Genetics
|
October 1, 1994
Distinct RB1 gene mutations with low penetrance in hereditary retinoblastoma
D R Lohmann, B Brandt, W Höpping, et al.
Human Genetics
|
July 1, 1987
Detection of submicroscopic deletions and a DNA polymorphism at the retinoblastoma locus
B Horsthemke, V Greger, H J Barnert, et al.
Cancer Genetics and Cytogenetics
|
December 5, 2000
Identification of chromosomes 3, 6, and 8 aberrations in uveal melanoma by microsatellite analysis in comparison to comparative genomic hybridization
F Tschentscher, G Prescher, M Zeschnigk, et al.
American Journal of Human Genetics
|
May 1, 1996
The spectrum of RB1 germ-line mutations in hereditary retinoblastoma
D R Lohmann, B Brandt, W Höpping, et al.
Lancet (London, England)
|
February 28, 1987
Early diagnosis in hereditary retinoblastoma by detection of molecular deletions at gene locus
B Horsthemke, H J Barnert, V Greger, et al.
Journal of Medical Genetics
|
April 1, 1988
Application of linkage analysis to genetic counselling in families with hereditary retinoblastoma
V Greger, S Kerst, E Messmer, et al.
European Journal of Biochemistry
|
September 22, 1999
Human TRH-degrading ectoenzyme cDNA cloning, functional expression, genomic structure and chromosomal assignment
L Schomburg, S Turwitt, G Prescher, et al.
Page
of 18
Search research articles
Search
Showing results (71-80 of 176) with videos related to
Sort By:
Page
of 18
Human Genetics
|
July 1, 1993
Rapid detection of trisomy 21 by quantitative PCR
F von Eggeling, M Freytag, R Fahsold, et al.
Verhandlungen Der Deutschen Gesellschaft Fur Innere Medizin
|
January 1, 1986
DNA deletions and DNA polymorphisms of the low density lipoprotein (LDL) receptor gene--their use in diagnosis
S E Humphries, A Dunning, R Taylor, et al.
Human Molecular Genetics
|
August 1, 1993
A BanII RFLP in the ZNF34 zinc finger gene on chromosome 8
B La Pillo, H J Lüdecke, H J Thiesen, et al.
Human Genetics
|
October 1, 1994
Distinct RB1 gene mutations with low penetrance in hereditary retinoblastoma
D R Lohmann, B Brandt, W Höpping, et al.
Human Genetics
|
July 1, 1987
Detection of submicroscopic deletions and a DNA polymorphism at the retinoblastoma locus
B Horsthemke, V Greger, H J Barnert, et al.
Cancer Genetics and Cytogenetics
|
December 5, 2000
Identification of chromosomes 3, 6, and 8 aberrations in uveal melanoma by microsatellite analysis in comparison to comparative genomic hybridization
F Tschentscher, G Prescher, M Zeschnigk, et al.
American Journal of Human Genetics
|
May 1, 1996
The spectrum of RB1 germ-line mutations in hereditary retinoblastoma
D R Lohmann, B Brandt, W Höpping, et al.
Lancet (London, England)
|
February 28, 1987
Early diagnosis in hereditary retinoblastoma by detection of molecular deletions at gene locus
B Horsthemke, H J Barnert, V Greger, et al.
Journal of Medical Genetics
|
April 1, 1988
Application of linkage analysis to genetic counselling in families with hereditary retinoblastoma
V Greger, S Kerst, E Messmer, et al.
European Journal of Biochemistry
|
September 22, 1999
Human TRH-degrading ectoenzyme cDNA cloning, functional expression, genomic structure and chromosomal assignment
L Schomburg, S Turwitt, G Prescher, et al.
Page
of 18