| scholarly article | Q13442814 |
| P356 | DOI | 10.1089/10906570050114894 |
| P698 | PubMed publication ID | 10953958 |
| P50 | author | Antonella Roetto | Q30004382 |
| Marco De Gobbi | Q53026545 | ||
| Enrico Bertino | Q56520665 | ||
| P2093 | author name string | C Fabris | |
| P Fortina | |||
| A M Gomez | |||
| C Camaschella | |||
| G Restagno | |||
| L Sbaiz | |||
| G C Fiorucci | |||
| P433 | issue | 2 | |
| P304 | page(s) | 177-181 | |
| P577 | publication date | 2000-01-01 | |
| P1433 | published in | Genetic Testing and Molecular Biomarkers | Q15753742 |
| P1476 | title | A pilot C282Y hemochromatosis screening in Italian newborns by TaqMan technology | |
| P478 | volume | 4 |
| Q52806667 | Comparative study of the two more frequent HFE mutations (C282Y and H63D): significant different allelic frequencies between the North and South of Portugal. |
| Q33307049 | Prevalence of H63D, S65C and C282Y hereditary hemochromatosis gene mutations in Slovenian population by an improved high-throughput genotyping assay |
| Q46931196 | Prevalence of HFE mutations in California newborns |
| Q38862702 | Prevalence of HFE mutations in people from North Africa living in southern France. |
| Q44394006 | Prevalence of HFE mutations in upper Northern Italy: study of 1132 unrelated blood donors. |
| Q35046454 | Public health aspects of genetic screening for hereditary haemochromatosis in Australia |
| Q38289955 | Rapid genotyping of single nucleotide polymorphisms using novel minor groove binding DNA oligonucleotides (MGB probes). |
| Q33833125 | Real-time PCR genotyping using displacing probes |
| Q35127374 | Single nucleotide polymorphism genotyping: biochemistry, protocol, cost and throughput |
| Q73304588 | Use of Denaturing HPLC and a Heteroduplex Generator to Detect the HFE C282Y Mutation Associated with Genetic Hemochromatosis |
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