112 related articles for article (PubMed ID: 2574085)
1. Prenatal diagnosis of alpha-1-antitrypsin deficiency using polymerase chain reaction (PCR). Comparison of conventional RFLP methods with PCR used in combination with allele specific oligonucleotides or RFLP analysis.
Schwartz M; Petersen KB; Gregersen N; Hinkel K; Newton CR
Clin Genet; 1989 Dec; 36(6):419-26. PubMed ID: 2574085
[TBL] [Abstract][Full Text] [Related]
2. First-trimester prenatal molecular diagnosis of infantile hypophosphatasia in a Japanese family.
Orimo H; Nakajima E; Hayashi Z; Kijima K; Watanabe A; Tenjin H; Araki T; Shimada T
Prenat Diagn; 1996 Jun; 16(6):559-63. PubMed ID: 8809899
[TBL] [Abstract][Full Text] [Related]
3. [The prenatal diagnosis of hemophilia A--the use of PCR and family RFLP analysis].
Bian M
Zhongguo Yi Xue Ke Xue Yuan Xue Bao; 1993 Apr; 15(2):102-7. PubMed ID: 7902217
[TBL] [Abstract][Full Text] [Related]
4. Prenatal exclusion testing for Huntington disease using the polymerase chain reaction.
McIntosh I; Curtis A; Millan FA; Brock DJ
Am J Med Genet; 1989 Feb; 32(2):274-6. PubMed ID: 2564738
[TBL] [Abstract][Full Text] [Related]
5. An alternate nonisotopic technique of PCR-mediated allele-specific oligonucleotide analysis for the detection of a point mutation.
Nakajima H; Hamaguchi T; Tomita K; Uenaka R; Yamagata K; Hanafusa T; Kuwajima M; Noguchi T; Tanaka T; Kono N
Res Commun Chem Pathol Pharmacol; 1993 Jan; 79(1):3-10. PubMed ID: 8434131
[TBL] [Abstract][Full Text] [Related]
6. The use of DNA amplification for genetic counselling related diagnosis in haemophilia B.
Tsang TC; Bentley DR; Nilsson IM; Giannelli F
Thromb Haemost; 1989 Jun; 61(3):343-7. PubMed ID: 2572072
[TBL] [Abstract][Full Text] [Related]
7. Comprehensive typing of HLA-DPB1 alleles by polymerase chain reaction-restriction fragment length polymorphism (PCR-RFLP).
Sengar DP; Hampton N; Goldstein R; Sengar AS
Clin Invest Med; 1995 Dec; 18(6):465-72. PubMed ID: 8714790
[TBL] [Abstract][Full Text] [Related]
8. Rapid and inexpensive detection of alpha1-antitrypsin deficiency-related alleles S and Z by a real-time polymerase chain reaction suitable for a large-scale population-based screening.
Kaczor MP; Sanak M; Szczeklik A
J Mol Diagn; 2007 Feb; 9(1):99-104. PubMed ID: 17251342
[TBL] [Abstract][Full Text] [Related]
9. Rapid DNA analysis of alpha 1-antitrypsin deficiency: application of an improved method for amplifying mutated gene sequences.
Dermer SJ; Johnson EM
Lab Invest; 1988 Sep; 59(3):403-8. PubMed ID: 3261817
[TBL] [Abstract][Full Text] [Related]
10. DNA-based prenatal diagnosis of heritable skin diseases.
Christiano AM; Uitto J
Arch Dermatol; 1993 Nov; 129(11):1455-9. PubMed ID: 7902070
[TBL] [Abstract][Full Text] [Related]
11. Rapid, nonradioactive detection of mutations in the human genome by allele-specific amplification.
Okayama H; Curiel DT; Brantly ML; Holmes MD; Crystal RG
J Lab Clin Med; 1989 Aug; 114(2):105-13. PubMed ID: 2787825
[TBL] [Abstract][Full Text] [Related]
12. Accurate prenatal diagnosis of Hb Bart's hydrops fetalis in daily practice with a double-check PCR system.
Karnpean R; Fucharoen G; Fucharoen S; Sae-ung N; Sanchaisuriya K; Ratanasiri T
Acta Haematol; 2009; 121(4):227-33. PubMed ID: 19546525
[TBL] [Abstract][Full Text] [Related]
13. PCR amplification of specific alleles (PASA) is a general method for rapidly detecting known single-base changes.
Sommer SS; Groszbach AR; Bottema CD
Biotechniques; 1992 Jan; 12(1):82-7. PubMed ID: 1734929
[TBL] [Abstract][Full Text] [Related]
14. Rapid assignment of the swine major histocompatibility complex (SLA) class I and II genotypes in Clawn miniature swine using PCR-SSP and PCR-RFLP methods.
Ando A; Ota M; Sada M; Katsuyama Y; Goto R; Shigenari A; Kawata H; Anzai T; Iwanaga T; Miyoshi Y; Fujimura N; Inoko H
Xenotransplantation; 2005 Mar; 12(2):121-6. PubMed ID: 15693842
[TBL] [Abstract][Full Text] [Related]
15. Denaturing gradient gel electrophoresis of the alpha 1-antitrypsin gene: application to prenatal diagnosis.
Dubel JR; Finwick R; Hejtmancik JF
Am J Med Genet; 1991 Oct; 41(1):39-43. PubMed ID: 1951462
[TBL] [Abstract][Full Text] [Related]
16. Familial gene analysis for Wilson disease from north-west Indian patients.
Kumar S; Thapa BR; Kaur G; Prasad R
Ann Hum Biol; 2006; 33(2):177-86. PubMed ID: 16684691
[TBL] [Abstract][Full Text] [Related]
17. [Molecular characterization of two variants of alpha-1-antitrypsin deficiency: PI Mpalermo and PI Plovel].
Jardí R; Rodríguez-Frías F; Casas F; Cotrina M; Vidal R; Miravitlles M; Pascual C
Med Clin (Barc); 1997 Oct; 109(12):463-6. PubMed ID: 9441182
[TBL] [Abstract][Full Text] [Related]
18. [Analysis of alpha 1-antitrypsin deficiency using DNA methods].
Wick U; Kühnl P; Engel W
Monatsschr Kinderheilkd; 1990 Aug; 138(8):438-42. PubMed ID: 2215506
[TBL] [Abstract][Full Text] [Related]
19. [Genetic analyses of the ABO blood groups and application of the clinical laboratories].
Hosoi E
Rinsho Byori; 1997 Feb; 45(2):148-56. PubMed ID: 9120999
[TBL] [Abstract][Full Text] [Related]
20. [An alpha-1-antitrypsin deficiency allele PI*Siiyama found in a disputed paternity case].
Umetsu K; Yuasa I; Watanabe G; Ding M; Suzuki T
Nihon Hoigaku Zasshi; 1996 Feb; 50(1):37-40. PubMed ID: 8851088
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
