Similar articles for PMID: 12833420

Year	Number of Results
1993	2
1995	4
1996	1
1997	4
1998	3
1999	4
2000	6
2001	2
2002	4
2003	5
2004	7
2005	2
2006	5
2007	3
2008	4
2009	6
2010	6
2011	7
2012	5
2013	3
2014	4
2015	3
2016	5
2017	6
2018	2
2019	4
2020	3
2021	1
2022	1
2024	0

1

Two novel null mutations in a Taiwanese cystic fibrosis patient and a survey of East Asian CFTR mutations.

Wong LJ, Alper OM, Wang BT, Lee MH, Lo SY. Wong LJ, et al. Am J Med Genet A. 2003 Jul 15;120A(2):296-8. doi: 10.1002/ajmg.a.20039. Am J Med Genet A. 2003. PMID: 12833420 Review. No abstract available.

2

Detection of novel CFTR mutations in Taiwanese cystic fibrosis patients.

Alper OM, Shu SG, Lee MH, Wang BT, Lo SY, Lin KL, Chiu YL, Wong LJ. Alper OM, et al. J Formos Med Assoc. 2003 May;102(5):287-91. J Formos Med Assoc. 2003. PMID: 12874665

3

1154insTC is not a rare CFTR mutation.

Alper OM, Wong LJ, Hostetter G, Cook J, Tenenholz B, Hsu E, Woo MS. Alper OM, et al. Am J Med Genet A. 2003 Jul 15;120A(2):294-5. doi: 10.1002/ajmg.a.20038. Am J Med Genet A. 2003. PMID: 12833419 No abstract available.

4

Outcome of intracytoplasmic sperm injection for a couple in which the man is carrier of CFTR p.[R74W;V201M;D1270N] and p.P841R mutations and his spouse a heterozygous carrier of p.F508del mutation of the cystic fibrosis transmembrane conductance regulator gene.

Brugnon F, Bilan F, Heraud MC, Grizard G, Janny L, Creveaux I. Brugnon F, et al. Fertil Steril. 2008 Nov;90(5):2004.e23-6. doi: 10.1016/j.fertnstert.2008.05.057. Epub 2008 Aug 13. Fertil Steril. 2008. PMID: 18703181 Free article.

5

Phenotype and genotype of two Taiwanese cystic fibrosis siblings and a survey of delta F508 in East Asians.

Lin CJ, Chang SP, Ke YY, Chiu HY, Tsao LY, Chen M. Lin CJ, et al. Pediatr Neonatol. 2008 Dec;49(6):240-4. doi: 10.1016/S1875-9572(09)60018-8. Pediatr Neonatol. 2008. PMID: 19166122 Free article.

6

Two novel frameshift deletions (1924del7, 2055del9-->A) in the CFTR gene in Mexican cystic fibrosis patients.

Orozco L, Zielenski J, Markiewicz D, Villarreal T, Tsui LC, Lezana JL, del Angel RM. Orozco L, et al. Hum Mutat. 1997;10(3):239-40. doi: 10.1002/(SICI)1098-1004(1997)10:3<239::AID-HUMU11>3.0.CO;2-0. Hum Mutat. 1997. PMID: 9298826 No abstract available.

7

Clinical implications of cystic fibrosis transmembrane conductance regulator mutations.

Mickle JE, Cutting GR. Mickle JE, et al. Clin Chest Med. 1998 Sep;19(3):443-58, v. doi: 10.1016/s0272-5231(05)70092-7. Clin Chest Med. 1998. PMID: 9759548 Free article. Review.

8

Secondhand Smoke Exposure and Serum Trypsinogen in Cystic Fibrosis Carriers.

Ellery KM, Kopp B, Conwell DL, Gariepy C. Ellery KM, et al. Pancreas. 2019 Oct;48(9):1155-1159. doi: 10.1097/MPA.0000000000001401. Pancreas. 2019. PMID: 31593019

9

Cystic fibrosis: experience in one institution.

Liu LC, Shyur SD, Chu SH, Huang LH, Kao YH, Lei WT, Cheng CH, Lo CY, Chen CK, Fang LC. Liu LC, et al. J Microbiol Immunol Infect. 2014 Aug;47(4):358-61. doi: 10.1016/j.jmii.2012.06.005. Epub 2012 Sep 16. J Microbiol Immunol Infect. 2014. PMID: 22992393 Free article.

10

Prenatal and newborn screening for CFTR mutations: the difficulties of prediction.

Schwarz MJ. Schwarz MJ. Clin Biochem. 2011 May;44(7):485-486. doi: 10.1016/j.clinbiochem.2011.02.018. Clin Biochem. 2011. PMID: 22036338 No abstract available.

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