Literature DB >> 2857314

Prenatal diagnosis for alpha 1-antitrypsin deficiency.

D W Cox, T Mansfield.   

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Year:  1985        PMID： 2857314     DOI： 10.1016/s0140-6736(85)92078-1

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


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  4 in total

Review 1.  Diagnosis of genetic disease using recombinant DNA.

Authors:  D N Cooper; J Schmidtke
Journal:  Hum Genet       Date:  1986-05       Impact factor: 4.132

2.  Diagnosis of alpha 1-antitrypsin deficiency by enzymatic amplification of human genomic DNA and direct sequencing of polymerase chain reaction products.

Authors:  C R Newton; N Kalsheker; A Graham; S Powell; A Gammack; J Riley; A F Markham
Journal:  Nucleic Acids Res       Date:  1988-09-12       Impact factor: 16.971

3.  Physical mapping of four serpin genes: alpha 1-antitrypsin, alpha 1-antichymotrypsin, corticosteroid-binding globulin, and protein C inhibitor, within a 280-kb region on chromosome I4q32.1.

Authors:  G D Billingsley; M A Walter; G L Hammond; D W Cox
Journal:  Am J Hum Genet       Date:  1993-02       Impact factor: 11.025

4.  Prenatal diagnosis of alpha 1 antitrypsin deficiency and estimates of fetal risk for disease.

Authors:  D W Cox; T Mansfield
Journal:  J Med Genet       Date:  1987-01       Impact factor: 6.318
  4 in total

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