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Literature DB >> 6291862

Strategies for detecting and characterizing restriction fragment length polymorphisms (RFLP's).

M H Skolnick, R White.

Abstract

Mesh：

Substances：
DNA Restriction Enzymes

Year: 1982 PMID： 6291862 DOI： 10.1159/000131687

Source DB: PubMed Journal: Cytogenet Cell Genet ISSN： 0301-0171

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27 in total

1. Novel detection of restriction fragment length polymorphisms in the human major histocompatibility complex.

Authors: S J Cross; S Tonks; J Trowsdale; R D Campbell
Journal: Immunogenetics Date: 1991 Impact factor: 2.846

2. Improved carrier detection of haemophilia A using novel RFLPs at the DXS115 (767) locus.

Authors: P Jedlicka; S Greer; D S Millar; C B Grundy; E Jenkins; M Mitchell; R S Mibashan; V V Kakkar; D N Cooper
Journal: Hum Genet Date: 1990-08 Impact factor: 4.132

3. TaqI polymorphism in the LDL receptor gene and a TaqI 1.5-kb band associated with familial hypercholesterolemia.

Authors: K Yamakawa; T Okafuji; Y Iwamura; K Yuzawa; J Satoh; N Hattori; Y Yamanouchi; H Yanagi; K Kawai; S Tsuchiya
Journal: Hum Genet Date: 1988-09 Impact factor: 4.132

4. A systematic approach for detecting high-frequency restriction fragment length polymorphisms using large genomic probes.

Authors: J Feder; L Yen; E Wijsman; L Wang; L Wilkins; J Schroder; N Spurr; H Cann; M Blumenberg; L L Cavalli-Sforza
Journal: Am J Hum Genet Date: 1985-07 Impact factor: 11.025

10. Unusual scarcity of restriction site polymorphism in the human thyroglobulin gene. A linkage study suggesting autosomal dominance of a defective thyroglobulin allele.

Authors: F Baas; H Bikker; G J van Ommen; J J de Vijlder
Journal: Hum Genet Date: 1984 Impact factor: 4.132

Strategies for detecting and characterizing restriction fragment length polymorphisms (RFLP's).

1. Novel detection of restriction fragment length polymorphisms in the human major histocompatibility complex.

2. Improved carrier detection of haemophilia A using novel RFLPs at the DXS115 (767) locus.

3. TaqI polymorphism in the LDL receptor gene and a TaqI 1.5-kb band associated with familial hypercholesterolemia.

4. A systematic approach for detecting high-frequency restriction fragment length polymorphisms using large genomic probes.

5. Two new polymorphic markers in the human pro alpha 2(1) collagen gene.

6. An estimate of unique DNA sequence heterozygosity in the human genome.

7. Overabundance of rare-cutting restriction endonuclease sites in the human genome.

8. The human chromogranin A gene: chromosome assignment and RFLP analysis.

9. Combined tetrahydrobiopterin-phenylalanine loading test in the detection of partially defective biopterin synthesis.

10. Unusual scarcity of restriction site polymorphism in the human thyroglobulin gene. A linkage study suggesting autosomal dominance of a defective thyroglobulin allele.