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Results of search for 'su:"Polymorphism, Restriction Fragment Length"', page 1309 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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English
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Results
26161.
Association of TAP1 and TAP2 with systemic sclerosis in Japanese.
[electronic resource]
by
Takeuchi, F
Kuwata, S
Nakano, K
Nabeta, H
Hong, G H
Shibata, Y
Tanimoto, K
Ito, K
Producer:
19970220
In:
Clinical and experimental rheumatology
vol. 14
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26162.
Cloning and characterization of a locus encoding an indolepyruvate decarboxylase involved in indole-3-acetic acid synthesis in Erwinia herbicola.
[electronic resource]
by
Brandl, M T
Lindow, S E
Producer:
19970108
In:
Applied and environmental microbiology
vol. 62
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26163.
Identification of novel cry-type genes from Bacillus thuringiensis strains on the basis of restriction fragment length polymorphism of the PCR-amplified DNA.
[electronic resource]
by
Kuo, W S
Chak, K F
Producer:
19970102
In:
Applied and environmental microbiology
vol. 62
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26164.
Lack of association between the MHC linked OTF3 gene and systemic lupus erythematosus.
[electronic resource]
by
Pablos, J L
Carreira, P E
Gomez-Reino, J J
Producer:
19960305
In:
Lupus
vol. 4
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26165.
PCR haplotypes for the human Y chromosome based on alphoid satellite DNA variants and heteroduplex analysis.
[electronic resource]
by
Santos, F R
Pena, S D
Tyler-Smith, C
Producer:
19960122
In:
Gene
vol. 165
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26166.
Identification of recurrent and novel mutations in exon 4 of the LDL receptor gene in patients with familial hypercholesterolemia in the United Kingdom.
[electronic resource]
by
Gudnason, V
King-Underwood, L
Seed, M
Sun, X M
Soutar, A K
Humphries, S E
Producer:
19930222
In:
Arteriosclerosis and thrombosis : a journal of vascular biology
vol. 13
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26167.
Patterns of hepatitis B virus DNA integration in liver tissue of children with chronic infections.
[electronic resource]
by
Goto, Y
Yoshida, J
Kuzushima, K
Terashima, M
Morishima, T
Producer:
19930312
In:
Journal of pediatric gastroenterology and nutrition
vol. 16
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26168.
Brief report: donor-derived long-term multilineage hematopoiesis in a liver-transplant recipient.
[electronic resource]
by
Collins, R H
Anastasi, J
Terstappen, L W
Nikaein, A
Feng, J
Fay, J W
Klintmalm, G
Stone, M J
Producer:
19930324
In:
The New England journal of medicine
vol. 328
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26169.
Prevalence of CYP2D6 gene duplication and its repercussion on the oxidative phenotype in a white population.
[electronic resource]
by
Agúndez, J A
Ledesma, M C
Ladero, J M
Benítez, J
Producer:
19950504
In:
Clinical pharmacology and therapeutics
vol. 57
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26170.
P53 tumor suppressor gene in chronic myelogenous leukemia: a sequential study.
[electronic resource]
by
Rovira, A
Urbano-Ispizua, A
Cervantes, F
Rozman, M
Vives-Corrons, J L
Montserrat, E
Rozman, C
Producer:
19950522
In:
Annals of hematology
vol. 70
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26171.
An Ala/Thr variation in the coding region of the human cystatin C gene (CST3) detected as a SstII polymorphism.
[electronic resource]
by
Balbín, M
Grubb, A
Abrahamson, M
Producer:
19931012
In:
Human genetics
vol. 92
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26172.
The OLFR1 gene encoding the HGMP07E putative olfactory receptor maps to the 17p13-->p12 region of the human genome and reveals an MspI restriction fragment length polymorphism.
[electronic resource]
by
Schurmans, S
Muscatelli, F
Miot, F
Mattei, M G
Vassart, G
Parmentier, M
Producer:
19930610
In:
Cytogenetics and cell genetics
vol. 63
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26173.
Thyroxine binding in a TTR Met 119 kindred.
[electronic resource]
by
Alves, I L
Divino, C M
Schussler, G C
Altland, K
Almeida, M R
Palha, J A
Coelho, T
Costa, P P
Saraiva, M J
Producer:
19930909
In:
The Journal of clinical endocrinology and metabolism
vol. 77
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26174.
Multi-locus analysis of HLA class II genes in DR2-positive IDDM haplotypes in Finland. The "Childhood Diabetes in Finland" (DiMe) Study Group.
[electronic resource]
by
Reijonen, H
Ilonen, J
Akerblom, H K
Knip, M
Dosch, H M
Producer:
19940729
In:
Tissue antigens
vol. 43
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26175.
Multiple identification of a particular type of hereditary C1q deficiency in the Turkish population: review of the cases and additional genetic and functional analysis.
[electronic resource]
by
Petry, F
Berkel, A I
Loos, M
Producer:
19970731
In:
Human genetics
vol. 100
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26176.
Molecular typing of Streptococcus pneumoniae strains isolated in Romania.
[electronic resource]
by
Straut, M
Surdeanu, M
Ungureanu, V
Mihalcu, F
Pana, M
Producer:
19971209
In:
Advances in experimental medicine and biology
vol. 418
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26177.
A ras homologue of Neurospora crassa regulates morphology.
[electronic resource]
by
Kana-uchi, A
Yamashiro, C T
Tanabe, S
Murayama, T
Producer:
19970630
In:
Molecular & general genetics : MGG
vol. 254
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26178.
Identification of a new polymorphism in the human proteolipid protein gene.
[electronic resource]
by
Poduslo, S E
Decker, P
Astle, H
Kurth, J
LaBate, M
Producer:
19940110
In:
Neurochemistry international
vol. 23
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26179.
An additional HpaII polymorphism in exon 2 of the human platelet membrane glycoprotein IIIa gene.
[electronic resource]
by
Perichon, B
Clemenceau, S
Romand, A
Elion, J
Kaplan, C
Krishnamoorthy, R
Producer:
19940412
In:
Human genetics
vol. 93
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26180.
Likelihood analysis of disequilibrium mapping, and related problems.
[electronic resource]
by
Rannala, B
Slatkin, M
Producer:
19980406
In:
American journal of human genetics
vol. 62
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