Literature DB >> 2895285

Prenatal diagnosis of alpha-1-antitrypsin deficiency using polymerase chain reaction.

C M Abbott, C J McMahon, D B Whitehouse, S Povey.   

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Year:  1988        PMID： 2895285     DOI： 10.1016/s0140-6736(88)91565-6

Source DB:  PubMed          Journal:  Lancet        ISSN： 0140-6736            Impact factor:   79.321


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  6 in total

Review 1.  Application of the polymerase chain reaction to the diagnosis of human genetic disease.

Authors:  J Reiss; D N Cooper
Journal:  Hum Genet       Date:  1990-06       Impact factor: 4.132

Review 2.  The polymerase chain reaction: an improved method for the analysis of nucleic acids.

Authors:  H P Vosberg
Journal:  Hum Genet       Date:  1989-08       Impact factor: 4.132

3.  Rapid detection of alpha-1-antitrypsin deficiency by analysis of a PCR-induced TaqI restriction site.

Authors:  P J Dry
Journal:  Hum Genet       Date:  1991-10       Impact factor: 4.132

4.  Reliability of prenatal diagnosis of genetic diseases by analysis of amplified trophoblast DNA.

Authors:  M C Rosatelli; R Sardu; T Tuveri; M T Scalas; A Di Tucci; M De Murtas; G Loudianos; G Monni; A Cao
Journal:  J Med Genet       Date:  1990-04       Impact factor: 6.318

5.  A consortium approach to molecular genetic services. Scottish Molecular Genetics Consortium.

Authors:  D J Brock
Journal:  J Med Genet       Date:  1990-01       Impact factor: 6.318

6.  Human cytomegalovirus infection during childhood: detection of viral DNA in peripheral blood by means of polymerase chain reaction.

Authors:  M Shibata; T Morishima; M Terashima; H Kimura; K Kuzushima; N Hanada; K Nishikawa; K Watanabe
Journal:  Med Microbiol Immunol       Date:  1990       Impact factor: 3.402
  6 in total

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