These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
Pubmed for Handhelds
PUBMED FOR HANDHELDS
Journal Abstract Search
131 related items for PubMed ID: 10980555
1. A novel deletion in exon 12 (g1845delAG or g1846delGA) of the CFTR (ABCC7) gene in a CF infant presenting with meconium ileus. Seia M, Cantù-Rajnoldi A, Ambrosioni A, Fiori S, Prandoni S, Corbetta C, Bassotti A, Moretti E, Giunta A, Padoan R. Hum Mutat; 2000 Sep; 16(3):279. PubMed ID: 10980555 [No Abstract] [Full Text] [Related]
5. Association of the CLCA1 p.S357N variant with meconium ileus in European patients with cystic fibrosis. van der Doef HP, Slieker MG, Staab D, Alizadeh BZ, Seia M, Colombo C, van der Ent CK, Nickel R, Witt H, Houwen RH. J Pediatr Gastroenterol Nutr; 2010 Mar; 50(3):347-9. PubMed ID: 20179644 [Abstract] [Full Text] [Related]
7. Identification of a novel mutation of CFTR gene in a Korean patient with cystic fibrosis. Ko JM, Kim GH, Kim KM, Hong SJ, Yoo HW. J Korean Med Sci; 2008 Oct; 23(5):912-5. PubMed ID: 18955805 [Abstract] [Full Text] [Related]
8. A new frameshift mutation 460delG in exon 4 of the cystic fibrosis transmembrane conductance regulator (CFTR) gene. Wagner K, Schneditz P, Rosenkranz W. Hum Mutat; 1996 Oct; 7(2):183. PubMed ID: 8829644 [No Abstract] [Full Text] [Related]
11. A large deletion causes apparent homozygosity for the D1152H mutation in the cystic fibrosis transmembrane regulator (CFTR) gene. Diana A, Tesse R, Polizzi AM, Santostasi T, Manca A, Leonetti G, Seia M, Porcaro L, Cavallo L. Gene; 2012 Apr 10; 497(1):90-2. PubMed ID: 22310382 [Abstract] [Full Text] [Related]
14. Identification of a novel mutation (525del T) in exon 4 of the CFTR gene in a patient with cystic fibrosis. Kusic J, Radojkovic D, Cuppens H, Jaspers M, Tomic J, Savic A. Hum Mutat; 1999 Oct 10; 14(4):357. PubMed ID: 10502789 [No Abstract] [Full Text] [Related]