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Results of search for 'su:"Polymorphism, Restriction Fragment Length"', page 1262 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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25221.
Influence of apolipoproteins on the anatomical distribution of arterial disease.
[electronic resource]
by
Wiseman, S A
Powell, J T
Barber, N
Humphries, S E
Greenhalgh, R M
Producer:
19920330
In:
Atherosclerosis
vol. 89
Online resources:
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25222.
Costs and benefits of prenatal screening for cystic fibrosis.
[electronic resource]
by
Garber, A M
Fenerty, J P
Producer:
19910530
In:
Medical care
vol. 29
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25223.
HLA-DRB and DQB typing by a combination of serology, restriction fragment length polymorphism analysis and oligonucleotide probing.
[electronic resource]
by
Doherty, D G
Donaldson, P T
Producer:
19910819
In:
European journal of immunogenetics : official journal of the British Society for Histocompatibility and Immunogenetics
vol. 18
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25224.
The identification of two mis-sense mutations at the PAH gene locus in a Turkish patient with phenylketonuria.
[electronic resource]
by
Konecki, D S
Schlotter, M
Trefz, F K
Lichter-Konecki, U
Producer:
19911002
In:
Human genetics
vol. 87
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25225.
Streptococcus pyogenes causing toxic-shock-like syndrome and other invasive diseases: clonal diversity and pyrogenic exotoxin expression.
[electronic resource]
by
Musser, J M
Hauser, A R
Kim, M H
Schlievert, P M
Nelson, K
Selander, R K
Producer:
19910506
In:
Proceedings of the National Academy of Sciences of the United States of America
vol. 88
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25226.
Isolation of 1001 new markers from human chromosome 11, excluding the region of 11p13-p15.5, and their sublocalization by a new series of radiation-reduced somatic cell hybrids.
[electronic resource]
by
Gerhard, D S
Lawrence, E
Wu, J
Chua, H
Ma, N
Bland, S
Jones, C
Producer:
19920922
In:
Genomics
vol. 13
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25227.
Prenatal diagnosis of familial hypercholesterolemia caused by the "Lebanese" mutation at the low density lipoprotein receptor locus.
[electronic resource]
by
Reshef, A
Meiner, V
Dann, E J
Granat, M
Leitersdorf, E
Producer:
19920619
In:
Human genetics
vol. 89
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25228.
Restriction fragment length polymorphism analysis of the fimbrillin locus, fimA, of Porphyromonas gingivalis.
[electronic resource]
by
Loos, B G
Dyer, D W
Producer:
19920721
In:
Journal of dental research
vol. 71
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25229.
The DR3(w18),DQw4 haplotype differs from DR3(w17),DQw2 haplotypes at multiple class II loci.
[electronic resource]
by
Hurley, C K
Gregersen, P K
Gorski, J
Steiner, N
Robbins, F M
Hartzman, R
Johnson, A H
Silver, J
Producer:
19890612
In:
Human immunology
vol. 25
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25230.
The mouse neurological mutant weaver maps within the region of chromosome 16 that is homologous to human chromosome 21.
[electronic resource]
by
Reeves, R H
Crowley, M R
Lorenzon, N
Pavan, W J
Smeyne, R J
Goldowitz, D
Producer:
19900309
In:
Genomics
vol. 5
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25231.
Localization of fructose 6-P,2-kinase: fructose 2,6-bisphosphatase to human chromosome X.
[electronic resource]
by
Olson, S
Uyeda, K
McBride, O W
Producer:
19900125
In:
Somatic cell and molecular genetics
vol. 15
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25232.
Human microsomal xenobiotic epoxide hydrolase. Complementary DNA sequence, complementary DNA-directed expression in COS-1 cells, and chromosomal localization.
[electronic resource]
by
Skoda, R C
Demierre, A
McBride, O W
Gonzalez, F J
Meyer, U A
Producer:
19880225
In:
The Journal of biological chemistry
vol. 263
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25233.
Assignment to chromosome 11 of mouse p68 RNA helicase gene (Hlr1) and pseudogene (Hlr1-ps1).
[electronic resource]
by
Petry, P
Johnson, K R
Lemaire, L
Heinlein, U A
Producer:
19950530
In:
FEBS letters
vol. 363
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25234.
Clonal analysis of peripheral blood and haemopoietic colonies in patients with aplastic anaemia and refractory anaemia using the polymorphic short tandem repeat on the human androgen-receptor (HUMARA) gene.
[electronic resource]
by
Anan, K
Ito, M
Misawa, M
Ohe, Y
Kai, S
Kohsaki, M
Hara, H
Producer:
19950713
In:
British journal of haematology
vol. 89
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25235.
Pulsed-field gel electrophoretic identification of Salmonella enterica serovar Typhimurium live vaccine strain Zoosaloral H.
[electronic resource]
by
Schwarz, S
Liebisch, B
Producer:
19950210
In:
Letters in applied microbiology
vol. 19
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25236.
Protein and molecular characterization of hippocampal protein kinase C in C57BL/6 and DBA/2 mice.
[electronic resource]
by
Bowers, B J
Christensen, S C
Pauley, J R
Paylor, R
Yuva, L
Dunbar, S E
Wehner, J M
Producer:
19950628
In:
Journal of neurochemistry
vol. 64
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25237.
Molecular basis of long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency: identification of the major disease-causing mutation in the alpha-subunit of the mitochondrial trifunctional protein.
[electronic resource]
by
IJlst, L
Wanders, R J
Ushikubo, S
Kamijo, T
Hashimoto, T
Producer:
19950207
In:
Biochimica et biophysica acta
vol. 1215
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25238.
Association between chronic cutaneous lupus erythematosus and HLA class II alleles.
[electronic resource]
by
Fischer, G F
Pickl, W F
Faé, I
Anegg, B
Milota, S
Volc-Platzer, B
Producer:
19950412
In:
Human immunology
vol. 41
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25239.
Response to interferon-alpha of Egyptian patients infected with hepatitis C virus genotype 4.
[electronic resource]
by
el-Zayadi, A
Simmonds, P
Dabbous, H
Prescott, L
Selim, O
Ahdy, A
Producer:
19970303
In:
Journal of viral hepatitis
vol. 3
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25240.
Novel insertion mutation in a non-Jewish Caucasian type 1 Gaucher disease patient.
[electronic resource]
by
Choy, F Y
Humphries, M L
Ferreira, P
Producer:
19970425
In:
American journal of medical genetics
vol. 68
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