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Annals of Human Genetics
|
March 30, 2000
Characterization of polymorphisms in the promoter of the human angiotensin II subtype 1 (AT1) receptor gene
J Erdmann, K Riedel, K Rohde, et al.
American Journal of Human Genetics
|
May 5, 2000
Parametric and nonparametric multipoint linkage analysis with imprinting and two-locus-trait models: application to mite sensitization
K Strauch, R Fimmers, T Kurz, et al.
Transactions of the Ophthalmological Societies of the United Kingdom
|
January 1, 1986
Norrie's disease: delineation of carriers among daughters of obligate carriers by linkage analysis
M Warburg, U Friedrich, L Bleeker-Wagemakers, et al.
Human Genetics
|
January 1, 1985
Close linkage between Norrie disease, a cloned DNA sequence from the proximal short arm, and the centromere of the X chromosome
L M Bleeker-Wagemakers, U Friedrich, A Gal, et al.
Der Ophthalmologe : Zeitschrift Der Deutschen Ophthalmologischen Gesellschaft
|
September 20, 2005
[Y402H polymorphism in complement factor H and age-related macula degeneration (AMD)]
H P N Scholl, B H F Weber, M M Nöthen, et al.
American Journal of Human Genetics
|
December 5, 1998
The gene for human fibronectin glomerulopathy maps to 1q32, in the region of the regulation of complement activation gene cluster
M Vollmer, M Jung, F Rüschendorf, et al.
Human Heredity
|
January 1, 1991
New mutation versus exclusion at the alpha-1-antitrypsin locus: a multifaceted approach in a problematical paternity case
K Bender, D Kasulke, A Mayerovà, et al.
Respirology (Carlton, Vic.)
|
May 21, 2025
Feasibility of a Modified Bronchoscopic Transparenchymal Nodule Access Technique ('Essen Tunnel') for Improving the Diagnosis of Intraparenchymal Pulmonary Lesions
Erik Büscher, Faustina Funke, Jane Winantea, et al.
Forensic Science International. Genetics
|
October 26, 2010
Geostatistical inference of main Y-STR-haplotype groups in Europe
Amalia Diaz-Lacava, Maja Walier, Sascha Willuweit, et al.
American Journal of Human Genetics
|
April 17, 1999
Quantitative analysis of survival motor neuron copies: identification of subtle SMN1 mutations in patients with spinal muscular atrophy, genotype-phenotype correlation, and implications for genetic counseling
B Wirth, M Herz, A Wetter, et al.
Page
of 29
Search research articles
Search
Showing results (91-100 of 282) with videos related to
Sort By:
Page
of 29
Annals of Human Genetics
|
March 30, 2000
Characterization of polymorphisms in the promoter of the human angiotensin II subtype 1 (AT1) receptor gene
J Erdmann, K Riedel, K Rohde, et al.
American Journal of Human Genetics
|
May 5, 2000
Parametric and nonparametric multipoint linkage analysis with imprinting and two-locus-trait models: application to mite sensitization
K Strauch, R Fimmers, T Kurz, et al.
Transactions of the Ophthalmological Societies of the United Kingdom
|
January 1, 1986
Norrie's disease: delineation of carriers among daughters of obligate carriers by linkage analysis
M Warburg, U Friedrich, L Bleeker-Wagemakers, et al.
Human Genetics
|
January 1, 1985
Close linkage between Norrie disease, a cloned DNA sequence from the proximal short arm, and the centromere of the X chromosome
L M Bleeker-Wagemakers, U Friedrich, A Gal, et al.
Der Ophthalmologe : Zeitschrift Der Deutschen Ophthalmologischen Gesellschaft
|
September 20, 2005
[Y402H polymorphism in complement factor H and age-related macula degeneration (AMD)]
H P N Scholl, B H F Weber, M M Nöthen, et al.
American Journal of Human Genetics
|
December 5, 1998
The gene for human fibronectin glomerulopathy maps to 1q32, in the region of the regulation of complement activation gene cluster
M Vollmer, M Jung, F Rüschendorf, et al.
Human Heredity
|
January 1, 1991
New mutation versus exclusion at the alpha-1-antitrypsin locus: a multifaceted approach in a problematical paternity case
K Bender, D Kasulke, A Mayerovà, et al.
Respirology (Carlton, Vic.)
|
May 21, 2025
Feasibility of a Modified Bronchoscopic Transparenchymal Nodule Access Technique ('Essen Tunnel') for Improving the Diagnosis of Intraparenchymal Pulmonary Lesions
Erik Büscher, Faustina Funke, Jane Winantea, et al.
Forensic Science International. Genetics
|
October 26, 2010
Geostatistical inference of main Y-STR-haplotype groups in Europe
Amalia Diaz-Lacava, Maja Walier, Sascha Willuweit, et al.
American Journal of Human Genetics
|
April 17, 1999
Quantitative analysis of survival motor neuron copies: identification of subtle SMN1 mutations in patients with spinal muscular atrophy, genotype-phenotype correlation, and implications for genetic counseling
B Wirth, M Herz, A Wetter, et al.
Page
of 29