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Results of search for 'su:"Polymorphism, Restriction Fragment Length"', page 1190 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
23781.
Vitamin D receptor and binding protein polymorphisms in women with polycystic ovary syndrome: a case control study.
[electronic resource]
by
Song, Do Kyeong
Lee, Hyejin
Hong, Young Sun
Sung, Yeon-Ah
Producer:
20200519
In:
BMC endocrine disorders
vol. 19
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23782.
Molecular epidemiology of Tinea gladiatorum in contact sports in northern Iran.
[electronic resource]
by
Kermani, Firoozeh
Moosazadeh, Mahmood
Hedayati, Mohammad T
Abastabar, Mahdi
Haghani, Iman
Aghili, Seyed Reza
Shokohi, Tahereh
Producer:
20201106
In:
Mycoses
vol. 63
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23783.
Sperm typing allows accurate measurement of the recombination fraction between D3S2 and D3S3 on the short arm of human chromosome 3.
[electronic resource]
by
Hubert, R
Stanton, V P
Aburatani, H
Warren, J
Li, H
Housman, D E
Arnheim, N
Producer:
19920529
In:
Genomics
vol. 12
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23784.
Transkinetoplastidy--a novel phenomenon involving bulk alterations of mitochondrion-kinetoplast DNA of a trypanosomatid protozoan.
[electronic resource]
by
Lee, S Y
Lee, S T
Chang, K P
Producer:
19920508
In:
The Journal of protozoology
vol. 39
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23785.
A mutation in codon 717 of the CHO-K1 elongation factor 2 gene prevents the first step in the biosynthesis of diphthamide.
[electronic resource]
by
Foley, B T
Moehring, J M
Moehring, T J
Producer:
19920904
In:
Somatic cell and molecular genetics
vol. 18
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23786.
Uniparental isodisomy due to duplication of chromosome 21 occurring in somatic cells monosomic for chromosome 21.
[electronic resource]
by
Petersen, M B
Bartsch, O
Adelsberger, P A
Mikkelsen, M
Schwinger, E
Antonarakis, S E
Producer:
19920730
In:
Genomics
vol. 13
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23787.
Sequence differences between HLA-B and TNF distinguish different MHC ancestral haplotypes.
[electronic resource]
by
Abraham, L J
Leelayuwat, C
Grimsley, G
Degli-Esposti, M A
Mann, A
Zhang, W J
Christiansen, F T
Dawkins, R L
Producer:
19920709
In:
Tissue antigens
vol. 39
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23788.
EBV strain variation: geographical distribution and relation to disease state.
[electronic resource]
by
Abdel-Hamid, M
Chen, J J
Constantine, N
Massoud, M
Raab-Traub, N
Producer:
19921016
In:
Virology
vol. 190
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23789.
HLA-DRB1 genotyping by modified PCR-RFLP method combined with group-specific primers.
[electronic resource]
by
Ota, M
Seki, T
Fukushima, H
Tsuji, K
Inoko, H
Producer:
19921019
In:
Tissue antigens
vol. 39
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23790.
The baculovirus Autographa californica nuclear polyhedrosis virus genome includes a papain-like sequence.
[electronic resource]
by
Rawlings, N D
Pearl, L H
Buttle, D J
Producer:
19930408
In:
Biological chemistry Hoppe-Seyler
vol. 373
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23791.
HLA-DR/DQ gene variation in nongoitrous autoimmune thyroiditis at the serological and molecular level.
[electronic resource]
by
Bogner, U
Badenhoop, K
Peters, H
Schmieg, D
Mayr, W R
Usadel, K H
Schleusener, H
Producer:
19930701
In:
Autoimmunity
vol. 14
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23792.
Monozygotic twins with discordant sex.
[electronic resource]
by
Kurosawa, K
Kuromaru, R
Imaizumi, K
Nakamura, Y
Ishikawa, F
Ueda, K
Kuroki, Y
Producer:
19940203
In:
Acta geneticae medicae et gemellologiae
vol. 41
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23793.
Genetic counselling in Duchenne and Becker muscular dystrophy is problematic when carrier studies give controversial results.
[electronic resource]
by
Kääriäinen, H
Lindlöf, M
Somer, H
de la Chapelle, A
Producer:
19900516
In:
Clinical genetics
vol. 37
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23794.
Increased incidence of certain TCR and HLA genes associated with myasthenia gravis in Italians.
[electronic resource]
by
Mantegazza, R
Oksenberg, J R
Baggi, F
Antozzi, C
Illeni, M T
Pellegris, G
Cornelio, F
Steinman, L
Producer:
19901205
In:
Journal of autoimmunity
vol. 3
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23795.
Amerindian mitochondrial DNAs have rare Asian mutations at high frequencies, suggesting they derived from four primary maternal lineages.
[electronic resource]
by
Schurr, T G
Ballinger, S W
Gan, Y Y
Hodge, J A
Merriwether, D A
Lawrence, D N
Knowler, W C
Weiss, K M
Wallace, D C
Producer:
19900404
In:
American journal of human genetics
vol. 46
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23796.
Mapping X-linked ophthalmic diseases. IV. Provisional assignment of the locus for X-linked congenital cataracts and microcornea (the Nance-Horan syndrome) to Xp22.2-p22.3.
[electronic resource]
by
Lewis, R A
Nussbaum, R L
Stambolian, D
Producer:
19900425
In:
Ophthalmology
vol. 97
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23797.
Empty and occupied insertion site of the truncated LINE-1 repeat located in the mouse serum albumin-encoding gene.
[electronic resource]
by
Boccaccio, C
Deschatrette, J
Meunier-Rotival, M
Producer:
19900712
In:
Gene
vol. 88
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23798.
Amyloid beta protein precursor gene and hereditary cerebral hemorrhage with amyloidosis (Dutch).
[electronic resource]
by
Van Broeckhoven, C
Haan, J
Bakker, E
Hardy, J A
Van Hul, W
Wehnert, A
Vegter-Van der Vlis, M
Roos, R A
Producer:
19900626
In:
Science (New York, N.Y.)
vol. 248
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23799.
Tightly linked flanking markers for the Lowe oculocerebrorenal syndrome, with application to carrier assessment.
[electronic resource]
by
Reilly, D S
Lewis, R A
Ledbetter, D H
Nussbaum, R L
Producer:
19880526
In:
American journal of human genetics
vol. 42
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23800.
[TaqI restriction polymorphism and the HLA-B27 allele in ankylosing spondylitis].
[electronic resource]
by
Huetz, F
Lucotte, G
Kahan, A
Amor, B
Producer:
19870629
In:
Revue du rhumatisme et des maladies osteo-articulaires
vol. 54
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