Literature DB >> 2896232

Prenatal diagnosis and carrier detection of genetic diseases by analysis of deoxyribonucleic acid.

H Ostrer1, J F Hejtmancik.   

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Year:  1988        PMID: 2896232     DOI: 10.1016/s0022-3476(88)80682-6

Source DB:  PubMed          Journal:  J Pediatr        ISSN: 0022-3476            Impact factor:   4.406


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  5 in total

1.  PCR based diagnosis in the presence of 8% (v/v) blood.

Authors:  M Panaccio; A Lew
Journal:  Nucleic Acids Res       Date:  1991-03-11       Impact factor: 16.971

Review 2.  Inherited metabolic diseases affecting the carrier.

Authors:  W Endres
Journal:  J Inherit Metab Dis       Date:  1997-03       Impact factor: 4.982

3.  Rapid diagnosis of methicillin-resistant Staphylococcus aureus bacteremia by nested polymerase chain reaction.

Authors:  Y Kitagawa; M Ueda; N Ando; M Endo; K Ishibiki; Y Kobayashi; T Arai; M Kitajima
Journal:  Ann Surg       Date:  1996-11       Impact factor: 12.969

4.  Mutation analysis in Turkish phenylketonuria patients.

Authors:  M Ozgüç; I Ozalp; T Coşkun; E Yilmaz; H Erdem; S Ayter
Journal:  J Med Genet       Date:  1993-02       Impact factor: 6.318

5.  Framing utility: Regulatory reform and genetic tests in the USA, 1989-2000.

Authors:  Steve Sturdy
Journal:  Soc Sci Med       Date:  2020-03-19       Impact factor: 5.379

  5 in total

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