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A Case Control Study on the Contribution of Factor V-Leiden, Prothrombin G20210A, and MTHFR C677T Mutations to the Genetic Susceptibility of Deep Venous Thrombosis
Almawi, Wassim Y., Tamim, Hala, Kreidy, Raghid, Timson, Georgina, Rahal, Elias, Nabulsi, Malak, Finan, Ramzi R., Irani-Hakime, Noha
Published in Journal of thrombosis and thrombolysis (01.06.2005)
Published in Journal of thrombosis and thrombolysis (01.06.2005)
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Segregation Analysis of Restless Legs Syndrome: Possible Evidence for a Major Gene in a Family Study Using Blinded Diagnoses
Mathias, Rasika A., Hening, Wayne, Washburn, Mystinna, Allen, Richard P., Lesage, Suzanne, Wilson, Alexander F., Earley, Christopher J.
Published in Human heredity (01.01.2006)
Published in Human heredity (01.01.2006)
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Exon-primed intron-crossing (EPIC) PCR markers of Helicoverpa armigera (Lepidoptera: Noctuidae)
Tay, W.T., Behere, G.T., Heckel, D.G., Lee, S.F., Batterham, P.
Published in Bulletin of entomological research (01.10.2008)
Published in Bulletin of entomological research (01.10.2008)
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A genome-wide exploration suggests an oligogenic model of inheritance for the TAFI activity and its antigen levels
Sabater-Lleal, Maria, Buil, Alfonso, Souto, Juan Carlos, Alamsy, Laura, Borrell, Montserrat, Lathrop, Mark, Blangero, John, Fontcuberta, Jordi, Soria, José Manuel
Published in Human genetics (01.08.2008)
Published in Human genetics (01.08.2008)
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A single-tube quantitative high-resolution melting curve method for parent-of-origin determination of 15q duplications
Urraca, Nora, Davis, Lea, Cook, Jr, Edwin H, Schanen, N Carolyn, Reiter, Lawrence T
Published in Genetic testing and molecular biomarkers (01.08.2010)
Published in Genetic testing and molecular biomarkers (01.08.2010)
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A novel mutation of GDAP1 associated with Charcot-Marie-Tooth disease in three Italian families: evidence for a founder effect
Di Maria, E, Gulli, R, Balestra, P, Cassandrini, D, Pigullo, S, Doria-Lamba, L, Bado, M, Schenone, A, Ajmar, F, Mandich, P, Bellone, E
Published in Journal of neurology, neurosurgery and psychiatry (01.10.2004)
Published in Journal of neurology, neurosurgery and psychiatry (01.10.2004)
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Possible parent-of-origin effect of Dopa decarboxylase in susceptibility to bipolar affective disorder
Børglum, A.D., Kirov, G., Craddock, N., Mors, O., Muir, W., Murray, V., McKee, I., Collier, D.A., Ewald, H., Owen, M.J., Blackwood, D., Kruse, T.A.
Published in American journal of medical genetics. Part B, Neuropsychiatric genetics (15.02.2003)
Published in American journal of medical genetics. Part B, Neuropsychiatric genetics (15.02.2003)
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Specificity in the familial aggregation of overt and covert conduct disorder symptoms in a referred attention-deficit hyperactivity disorder sample
MONUTEAUX, M. C., FITZMAURICE, G., BLACKER, D., BUKA, S. L., BIEDERMAN, J.
Published in Psychological medicine (01.08.2004)
Published in Psychological medicine (01.08.2004)
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Association of Hb Q-Thailand with homozygous Hb E and heterozygous Hb Constant Spring in pregnancy
Sanchaisuriya, Kanokwan, Chunpanich, Sunisa, Fucharoen, Supan, Fucharoen, Goonnapa, Sanchaisuriya, Pattara, Changtrakun, Yossombat
Published in European journal of haematology (01.03.2005)
Published in European journal of haematology (01.03.2005)
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Contribution of Genetics and Environment to Craniofacial Anthropometric Phenotypes in Belgian Nuclear Families
Jelenkovic, Aline, Poveda, Alaitz, Susanne, Charles, Rebato, Esther
Published in Human biology (01.12.2008)
Published in Human biology (01.12.2008)
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Pleiotropic genetic effects contribute to the correlation between HDL cholesterol, triglycerides, and LDL particle size in hypertensive sibships
Kullo, Iftikhar J., de Andrade, Mariza, Boerwinkle, Eric, McConnell, Joseph P., Kardia, Sharon L.R., Turner, Stephen T.
Published in American journal of hypertension (2005)
Published in American journal of hypertension (2005)
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Novel mutations at carboxyl terminus of CIC-1 channel in myotonia congenita
Kuo, H.-C., Hsiao, K.-M., Chang, L.-I., You, T.-H., Yeh, T.-H., Huang, C.-C.
Published in Acta neurologica Scandinavica (01.05.2006)
Published in Acta neurologica Scandinavica (01.05.2006)
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Autism spectrum conditions in myotonic dystrophy type 1: a study on 57 individuals with congenital and childhood forms
Ekström, Anne-Berit, Hakenäs-Plate, Louise, Samuelsson, Lena, Tulinius, Már, Wentz, Elisabet
Published in American journal of medical genetics. Part B, Neuropsychiatric genetics (05.09.2008)
Published in American journal of medical genetics. Part B, Neuropsychiatric genetics (05.09.2008)
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