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For: Raynal C, Corvol H. Variant classifications, databases and genotype-phenotype correlations. Arch Pediatr 2020;27 Suppl 1:eS13-8. [PMID: 32172930 DOI: 10.1016/S0929-693X(20)30045-2] [Cited by in Crossref: 4] [Cited by in F6Publishing: 3] [Article Influence: 2.0] [Reference Citation Analysis]
Number Citing Articles
1 Françoise A, Héry-Arnaud G. The Microbiome in Cystic Fibrosis Pulmonary Disease. Genes (Basel) 2020;11:E536. [PMID: 32403302 DOI: 10.3390/genes11050536] [Cited by in Crossref: 16] [Cited by in F6Publishing: 13] [Article Influence: 8.0] [Reference Citation Analysis]
2 Mekki C, Aissat A, Mirlesse V, Mayer Lacrosniere S, Eche E, Le Floch A, Whalen S, Prud'Homme C, Remus C, Funalot B, Castaigne V, Fanen P, de Becdelièvre A. Prenatal Ultrasound Suspicion of Cystic Fibrosis in a Multiethnic Population: Is Extensive CFTR Genotyping Needed? Genes (Basel) 2021;12:670. [PMID: 33946859 DOI: 10.3390/genes12050670] [Reference Citation Analysis]
3 Ardizzone A, Capra AP, Campolo M, Filippone A, Esposito E, Briuglia S. Neurofibromatosis: New Clinical Challenges in the Era of COVID-19. Biomedicines 2022;10:940. [DOI: 10.3390/biomedicines10050940] [Reference Citation Analysis]
4 Castaldo A, Cimbalo C, Castaldo RJ, D'Antonio M, Scorza M, Salvadori L, Sepe A, Raia V, Tosco A. Cystic Fibrosis-Screening Positive Inconclusive Diagnosis: Newborn Screening and Long-Term Follow-Up Permits to Early Identify Patients with CFTR-Related Disorders. Diagnostics (Basel) 2020;10:E570. [PMID: 32784480 DOI: 10.3390/diagnostics10080570] [Cited by in Crossref: 4] [Cited by in F6Publishing: 4] [Article Influence: 2.0] [Reference Citation Analysis]