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Results of search for 'su:"Polymorphism, Restriction Fragment Length"', page 1744 of 1861
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Authors
Ballard, L
Copeland, N G
Dubey, J P
Gusella, J F
Humphries, S E
Inoko, H
Jenkins, N A
Kidd, K K
Lalouel, J M
Lathrop, G M
Lefranc, G
Lefranc, M P
Leppert, M
Nakamura, Y
O'Connell, P
Rothschild, M F
White, R
Xiao, Lihua
Zbar, B
van Soolingen, D
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Topics
Adult
Alleles
Animals
Base Sequence
Female
Gene Frequency
Genotype
Humans
Male
Middle Aged
Molecular Sequence Data
Polymerase Chain Reaction
Polymorphism, Genetic
Polymorphism, Restriction Fragment Length
analysis
classification
epidemiology
genetics
methods
microbiology
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Results
34861.
Molecular analysis of integron gene cassette arrays associated multi-drug resistant Enterobacteriaceae isolates from poultry.
[electronic resource]
by
El-Demerdash, Azza S
Aggour, Mohamed G
El-Azzouny, Mona M
Abou-Khadra, Sally H
Producer:
20180921
In:
Cellular and molecular biology (Noisy-le-Grand, France)
vol. 64
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34862.
Haplotypes of ABCB1 1236C >T (rs1128503), 2677G >T/A (rs2032582), and 3435C >T (rs1045642) in patients with bullous pemphigoid.
[electronic resource]
by
Rychlik-Sych, Mariola
Barańska, Małgorzata
Dudarewicz, Michał
Skrętkowicz, Jadwiga
Żebrowska, Agnieszka
Woźniacka, Anna
Owczarek, Jacek
Orszulak-Michalak, Daria
Waszczykowska, Elżbieta
Producer:
20181024
In:
Archives of dermatological research
vol. 310
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34863.
Clonal deletion of V beta 17 T cells in mice from natural populations.
[electronic resource]
by
Jouvin-Marche, E
Marche, P N
Cazenave, P A
Producer:
19930219
In:
Seminars in immunology
vol. 4
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34864.
Improved predictive test for MEN2, using flanking dinucleotide repeats and RFLPs.
[electronic resource]
by
Howe, J R
Lairmore, T C
Mishra, S K
Dou, S
Veile, R
Wells, S A
Donis-Keller, H
Producer:
19930114
In:
American journal of human genetics
vol. 51
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34865.
Contiguous localization of the genes encoding human insulin-like growth factor binding proteins 1 (IGBP1) and 3 (IGBP3) on chromosome 7.
[electronic resource]
by
Ehrenborg, E
Larsson, C
Stern, I
Janson, M
Powell, D R
Luthman, H
Producer:
19920514
In:
Genomics
vol. 12
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34866.
Tumor progression in four mammary epithelial cell lines derived from the same patient.
[electronic resource]
by
Band, V
Zajchowski, D
Swisshelm, K
Trask, D
Kulesa, V
Cohen, C
Connolly, J
Sager, R
Producer:
19901207
In:
Cancer research
vol. 50
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34867.
Restriction fragment length polymorphism analysis of major histocompatibility complex genes in the non-obese diabetic mouse strain and its non-diabetic sister strains.
[electronic resource]
by
Fujishima, Y
Koide, Y
Kaidoh, T
Nishimura, M
Yoshida, T O
Producer:
19890710
In:
Diabetologia
vol. 32
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34868.
Duplication and transcription of procyclin genes in Trypanosoma brucei.
[electronic resource]
by
König, E
Delius, H
Carrington, M
Williams, R O
Roditi, I
Producer:
19891227
In:
Nucleic acids research
vol. 17
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34869.
Individuals with IgA deficiency and common variable immunodeficiency share polymorphisms of major histocompatibility complex class III genes.
[electronic resource]
by
Schaffer, F M
Palermos, J
Zhu, Z B
Barger, B O
Cooper, M D
Volanakis, J E
Producer:
19891201
In:
Proceedings of the National Academy of Sciences of the United States of America
vol. 86
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34870.
Molecular cloning and expression of human tumor-associated polymorphic epithelial mucin.
[electronic resource]
by
Gendler, S J
Lancaster, C A
Taylor-Papadimitriou, J
Duhig, T
Peat, N
Burchell, J
Pemberton, L
Lalani, E N
Wilson, D
Producer:
19901009
In:
The Journal of biological chemistry
vol. 265
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34871.
Expression of intra-MHC transporter (Ham) genes and class I antigens in diabetes-susceptible NOD mice.
[electronic resource]
by
Gaskins, H R
Monaco, J J
Leiter, E H
Producer:
19920724
In:
Science (New York, N.Y.)
vol. 256
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34872.
Alterations in expression and structure of the DNA repair gene XRCC1.
[electronic resource]
by
Yoo, H
Li, L
Sacks, P G
Thompson, L H
Becker, F F
Chan, J Y
Producer:
19920904
In:
Biochemical and biophysical research communications
vol. 186
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34873.
Leu-676-Pro mutation of the androgen receptor causes complete androgen insensitivity syndrome in a large Hutterite kindred.
[electronic resource]
by
Belsham, D D
Pereira, F
Greenberg, C R
Liao, S
Wrogemann, K
Producer:
19950530
In:
Human mutation
vol. 5
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34874.
Linkage of 11 beta-hydroxylase mutations with altered steroid biosynthesis and blood pressure in the Dahl rat.
[electronic resource]
by
Cicila, G T
Rapp, J P
Wang, J M
St Lezin, E
Ng, S C
Kurtz, T W
Producer:
19950105
In:
Nature genetics
vol. 3
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34875.
Beta spectrin kissimmee: a spectrin variant associated with autosomal dominant hereditary spherocytosis and defective binding to protein 4.1.
[electronic resource]
by
Becker, P S
Tse, W T
Lux, S E
Forget, B G
Producer:
19930915
In:
The Journal of clinical investigation
vol. 92
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34876.
The apoB-100 gene EcoRI polymorphism influences the relationship between features of the insulin resistance syndrome and the hyper-apoB and dense LDL phenotype in men.
[electronic resource]
by
Vohl, M C
Tchernof, A
Dionne, F T
Moorjani, S
Prud'homme, D
Bouchard, C
Nadeau, A
Lupien, P J
Després, J P
Producer:
19961104
In:
Diabetes
vol. 45
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34877.
Apolipoprotein A-I/C-III/A-IV gene cluster in familial combined hyperlipidemia: effects on LDL-cholesterol and apolipoproteins B and C-III.
[electronic resource]
by
Dallinga-Thie, G M
Bu, X D
van Linde-Sibenius Trip, M
Rotter, J I
Lusis, A J
de Bruin, T W
Producer:
19961206
In:
Journal of lipid research
vol. 37
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34878.
Dopamine D2, D3 and D4 receptor and transporter gene polymorphisms and mood disorders.
[electronic resource]
by
Manki, H
Kanba, S
Muramatsu, T
Higuchi, S
Suzuki, E
Matsushita, S
Ono, Y
Chiba, H
Shintani, F
Nakamura, M
Yagi, G
Asai, M
Producer:
19970204
In:
Journal of affective disorders
vol. 40
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34879.
The gene for microfibril-associated protein-1 (MFAP1) is located several megabases centromeric to FBN1 and is not mutated in Marfan syndrome.
[electronic resource]
by
Liu, W
Faraco, J
Qian, C
Francke, U
Producer:
19970609
In:
Human genetics
vol. 99
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34880.
HLA class II and T-cell receptor beta chain polymorphisms in Belgian patients with rheumatoid arthritis: no evidence for disease association with the TCRBC2, TCRBV8 and TCRBV11 polymorphisms.
[electronic resource]
by
Vandevyver, C
Gu, X X
Geusens, P
Spaepen, M
Philippaerts, L
Cassiman, J J
Raus, J
Producer:
19941222
In:
Annals of the rheumatic diseases
vol. 53
Online resources:
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