Diagnosis of atypical CF: a case-report to reflect.

Alghisi, F; Angioni, A; Tomaiuolo, A C; D'Apice, M R; Bella, S; Novelli, G; Lucidi, V

Alghisi, F; Angioni, A; Tomaiuolo, A C; D'Apice, M R; Bella, S; Novelli, G; Lucidi, V.

Affiliation

Alghisi F; Unit of Cystic Fibrosis, Bambino Gesù Children's Hospital-Rome, Italy.
Angioni A; Laboratory of Cytogenetics and Molecular Genetics, Bambino Gesù Children's Hospital-Rome, Italy.
Tomaiuolo AC; Laboratory of Cytogenetics and Molecular Genetics, Bambino Gesù Children's Hospital-Rome, Italy.
D'Apice MR; Department of Biopathology and Diagnostic Imaging, Tor Vergata University-Rome, Italy.
Bella S; Unit of Cystic Fibrosis, Bambino Gesù Children's Hospital-Rome, Italy.
Novelli G; Department of Biopathology and Diagnostic Imaging, Tor Vergata University-Rome, Italy.
Lucidi V; Unit of Cystic Fibrosis, Bambino Gesù Children's Hospital-Rome, Italy. Electronic address: lucidi@opbg.net.

J Cyst Fibros ; 7(4): 292-294, 2008 Jul.

Article in En | MEDLINE | ID: mdl-18180206

Subject(s)

Cystic Fibrosis Transmembrane Conductance Regulator/genetics; Cystic Fibrosis/diagnosis; Cystic Fibrosis/genetics; Bronchiectasis/etiology; Cystic Fibrosis/complications; Female; Genetic Carrier Screening; Humans; Mutation; Pedigree; Young Adult

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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Cystic Fibrosis Transmembrane Conductance Regulator / Cystic Fibrosis Type of study: Diagnostic_studies / Etiology_studies Limits: Adult / Female / Humans Language: En Journal: J Cyst Fibros Year: 2008 Type: Article Affiliation country: Italy

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