Literature DB >> 1678079

Transient neonatal hypertrypsinaemia as test for delta F508 heterozygosity.

G Lucotte, J L Perignon, G Lenoir.   

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Year:  1991        PMID： 1678079     DOI： 10.1016/0140-6736(91)91634-7

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


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  2 in total

1.  CFTR mutations and IVS8-5T variant in newborns with hypertrypsinaemia and normal sweat test.

Authors:  C Castellani; A Bonizzato; G Mastella
Journal:  J Med Genet       Date:  1997-04       Impact factor: 6.318

Review 2.  Clinical Phenotypes of Cystic Fibrosis Carriers.

Authors:  Philip M Polgreen; Alejandro P Comellas
Journal:  Annu Rev Med       Date:  2022-01-27       Impact factor: 13.739
  2 in total

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