18q deletion in a cystic fibrosis infant, increased morbidity and challenge for correct treatment choices: a case report

• Asıl Yazarlar: Dester Silvia (Yazar), Fogazzi Annalisa (Yazar), Timpano Silviana (Yazar), Spinelli Elide (Yazar), Milianti Susanna (Yazar), Padoan Rita (Yazar)
• Materyal Türü: Kitap
• Baskı/Yayın Bilgisi: BMC, 2011-05-01T00:00:00Z.
• Konular: article
• Online Erişim: Connect to this object online.

<p>Abstract</p> <p>Cystic Fibrosis (CF) is the most frequent recessive disease of Caucasian patients. Association with other diseases or syndromes has previously been reported. Co-morbidity may be a challenge for clinicians, who have to face more severe problems.</p> <p>...