scholarly journals Allele frequency ofHinfI restriction fragment length polymorphism (RFLP) and dinucleotide repeat polymorphism in the wilms tumor gene (WT1) among the Japanese

1994 ◽  
Vol 39 (1) ◽  
pp. 207-208 ◽  
Author(s):  
Tadashi Matsumoto ◽  
Miho Okumura ◽  
Tomoko Sawai ◽  
Shigeru Aoki ◽  
Yoshiro Tsuji
Keyword(s):  
Restriction Fragment Length Polymorphism ◽  
Allele Frequency ◽  
Length Polymorphism ◽  
Fragment Length ◽  
Fragment Length Polymorphism ◽  
Wilms Tumor ◽  
Repeat Polymorphism ◽  
Dinucleotide Repeat Polymorphism ◽  
Tumor Gene ◽  
Restriction Fragment Length

Restriction Fragment Length Polymorphism in Soybean Germplasm of the Southern USA

Crop Science ◽  
1993 ◽  
Vol 33 (6) ◽  
pp. 1169-1176 ◽  
Author(s):  
H. T. Skorupska ◽  
R. C. Shoemaker ◽  
A. Warner ◽  
E. R. Shipe ◽  
W. C. Bridges
Keyword(s):  
Restriction Fragment Length Polymorphism ◽  
Restriction Fragment ◽  
Length Polymorphism ◽  
Fragment Length ◽  
Fragment Length Polymorphism ◽  
Soybean Germplasm ◽  
Restriction Fragment Length

scholarly journals A southern analysis of Rh blood group genes: association between restriction fragment length polymorphism patterns and Rh serotypes

Blood ◽  
1994 ◽  
Vol 83 (2) ◽  
pp. 566-572 ◽  
Author(s):  
CA Hyland ◽  
LC Wolter ◽  
YW Liew ◽  
A Saul
Keyword(s):  
Restriction Fragment Length Polymorphism ◽  
Blood Group ◽  
Restriction Fragment ◽  
Length Polymorphism ◽  
Fragment Length ◽  
Fragment Length Polymorphism ◽  
Gene Dosage ◽  
Southern Analysis ◽  
Rh Blood Group ◽  
Restriction Fragment Length

Abstract Polymorphisms within the Rh blood group system have been defined by serologic agglutination methods, but have not yet been defined at the DNA level. Two closely related genes associated with the Rh D antigen and with the Rh C/c and E/e antigens have been cloned. We used a Southern analysis incorporating probes to the 5′ and 3′ regions of the Rh C, E gene and D gene to identify polymorphisms associated with Rh C/c and E/e antigens, respectively. The D gene dosage could be determined by comparing the relative intensities of the D bands with bands from the 5′ and 3′ region of the Rh C, E gene. The concordance between restriction fragment length polymorphism (RFLP) patterns and serologic phenotypes for 102 randomly selected blood donors was 100% for C, e, and D, 94.8% for c, and 94.3% for E. The data are consistent with the sequences encoding the C/c epitopes residing on the 5′ side of those for the E/e epitopes. All samples discordant for the 3′ probe and E had the cE (r″) serotype. These data show that the gene coding for the cE serotype is different in Rh-positive and -negative individuals. The study demonstrates that Rh DNA typing, including D gene dosage measurements and Rh gene haplotyping, may supplement traditional serotyping methods in transfusion medicine.

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