These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
15. An improved method for prenatal diagnosis of genetic diseases by analysis of amplified DNA sequences. Application to hemophilia A. Kogan SC, Doherty M, Gitschier J. N Engl J Med; 1987 Oct 15; 317(16):985-90. PubMed ID: 3657865 [Abstract] [Full Text] [Related]
16. Characterization of the sequence of the normal alpha-1-antitrypsin M3 allele and function of the M3 protein. Curiel D, Laubach V, Vogelmeier C, Wurts L, Crystal RG. Am J Respir Cell Mol Biol; 1989 Dec 15; 1(6):471-7. PubMed ID: 2637759 [Abstract] [Full Text] [Related]
17. 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 01; 41(1):39-43. PubMed ID: 1951462 [Abstract] [Full Text] [Related]
18. 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 01; 36(6):419-26. PubMed ID: 2574085 [Abstract] [Full Text] [Related]
19. [Analysis of alpha 1-antitrypsin deficiency using DNA methods]. Wick U, Kühnl P, Engel W. Monatsschr Kinderheilkd; 1990 Aug 01; 138(8):438-42. PubMed ID: 2215506 [Abstract] [Full Text] [Related]
20. PAP: detection of ultra rare mutations depends on P* oligonucleotides: "sleeping beauties" awakened by the kiss of pyrophosphorolysis. Liu Q, Sommer SS. Hum Mutat; 2004 May 01; 23(5):426-36. PubMed ID: 15108273 [Abstract] [Full Text] [Related] Page: [Next] [New Search]