Academic literature on the topic '12q24 haplotype'
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Journal articles on the topic "12q24 haplotype"
Wakil, Salma M., Nzioka P. Muiya, Asma I. Tahir, Mohammed Al-Najai, Batoul Baz, Editha Andres, Nejat Mazhar, et al. "A New Susceptibility Locus for Myocardial Infarction, Hypertension, Type 2 Diabetes Mellitus, and Dyslipidemia on Chromosome 12q24." Disease Markers 2014 (2014): 1–10. http://dx.doi.org/10.1155/2014/291419.
Full textDegn, B., M. D. Lundorf, A. Wang, M. Vang, O. Mors, T. A. Kruse, and H. Ewald. "Further evidence for a bipolar risk gene on chromosome 12q24 suggested by investigation of haplotype sharing and allelic association in patients from the Faroe Islands." Molecular Psychiatry 6, no. 4 (July 2001): 450–55. http://dx.doi.org/10.1038/sj.mp.4000882.
Full textApostolou, P., M. Pertesi, V. Aleporou‐Marinou, C. Dimitrakakis, C. Papadimitriou, E. Razis, C. Christodoulou, et al. "Haplotype analysis reveals that the recurrent BRCA1 deletion of exons 23 and 24 is a Greek founder mutation." Clinical Genetics 91, no. 3 (August 22, 2016): 482–87. http://dx.doi.org/10.1111/cge.12824.
Full textLinnebank, Michael, Miroslav Janosik, Viktor Kozich, Ewa Pronicka, Jolanta Kubalska, Jitka Sokolova, Anja Linnebank, et al. "The cystathionine ?-synthase (CBS) mutation c.1224-2A>C in Central Europe: Vitamin B6 nonresponsiveness and a common ancestral haplotype." Human Mutation 24, no. 4 (2004): 352–53. http://dx.doi.org/10.1002/humu.9280.
Full textKalsi, Gursharan, Andrew McQuillin, Birte Degn, Mikkel D. Lundorf, Nicholas J. Bass, Jacob Lawrence, Khalid Choudhury, et al. "Identification of the Slynar Gene (AY070435) and Related Brain Expressed Sequences as a Candidate Gene for Susceptibility to Affective Disorders Through Allelic and Haplotypic Association With Bipolar Disorder on Chromosome 12q24." American Journal of Psychiatry 163, no. 10 (October 2006): 1767–76. http://dx.doi.org/10.1176/ajp.2006.163.10.1767.
Full textRaballah, Evans, Samuel B. Anyona, Qiuying Cheng, Elly O. Munde, Ivy-Foo Hurwitz, Clinton Onyango, Caroline Ndege, et al. "Complement component 3 mutations alter the longitudinal risk of pediatric malaria and severe malarial anemia." Experimental Biology and Medicine, November 29, 2021, 153537022110562. http://dx.doi.org/10.1177/15353702211056272.
Full textAron Badin, Romina, Aurore Bugi, Susannah Williams, Marta Vadori, Marie Michael, Caroline Jan, Alberto Nassi, et al. "MHC matching fails to prevent long-term rejection of iPSC-derived neurons in non-human primates." Nature Communications 10, no. 1 (September 25, 2019). http://dx.doi.org/10.1038/s41467-019-12324-0.
Full textDissertations / Theses on the topic "12q24 haplotype"
SPOLVERINI, AMBRA. "Analysis of polymorphic variants and new mutations in patients with Chronic Myeloporiliferative Neoplasms." Doctoral thesis, 2013. http://hdl.handle.net/2158/796256.
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