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
68 related items for PubMed ID: 3214245
1. [Approaching the gene of mucoviscidosis. New data]. Ferec C, Morin JF, Parent P, Jehanne M, Chabaud JJ, Gouedard G, Journel H, Saleun JP. Arch Fr Pediatr; 1988 Oct; 45(8):531-5. PubMed ID: 3214245 [Abstract] [Full Text] [Related]
3. Analysis of DNA probes for the prenatal diagnosis of cystic fibrosis. Dry PJ, Wake S, Robertson CF, Colley P, Sheffield LJ. Med J Aust; 1989 Aug 07; 151(3):131, 133-6. PubMed ID: 2569157 [Abstract] [Full Text] [Related]
10. [Analysis of various polymorphic markers of the CFTR gene in cystic fibrosis patients and healthy donors from the Moscow region]. Amosenko FA, Sazonova MA, Kapranov NI, Trubnikova IS, Kalinin VN. Genetika; 1995 Apr 07; 31(4):532-5. PubMed ID: 7607440 [Abstract] [Full Text] [Related]
16. [Portion of certain cystic fibrosis gene mutations and linkage dysequilibrium between the CFTR-gene locus and two DNA marker loci in Russian populations]. Petrova NV, Ginter EK, Kapranov NI, El'chinova GI. Genetika; 1994 Jul 07; 30(7):974-7. PubMed ID: 7525404 [Abstract] [Full Text] [Related]
18. Analysis of DNA polymorphism haplotypes linked to the cystic fibrosis locus in North American black and Caucasian families supports the existence of multiple mutations of the cystic fibrosis gene. Cutting GR, Antonarakis SE, Buetow KH, Kasch LM, Rosenstein BJ, Kazazian HH. Am J Hum Genet; 1989 Mar 07; 44(3):307-18. PubMed ID: 2563631 [Abstract] [Full Text] [Related]
19. [Molecular-genetic analysis of certain mutations of the "cystic fibrosis gene" in Moldavia. Characteristics of molecular markers and their linkage with various mutations]. Gimbovskaia SD, Kalinin VN, Ivashchenko TE, Baranov VS. Genetika; 1994 Dec 07; 30(12):1616-20. PubMed ID: 7534245 [Abstract] [Full Text] [Related]
20. Usefulness of linkage disequilibrium of KM-19 and XV-2c DNA probes for genetic counselling in a high-risk CF family. Chomel JC, Haliassos A, Tesson L, Mathieu M, Kaplan JC, Kitzis A. Prenat Diagn; 1989 Apr 07; 9(4):297-300. PubMed ID: 2717536 [Abstract] [Full Text] [Related] Page: [Next] [New Search]