Association of IL10-1082 and IFN-γ+874 Polymorphisms with Cervical Cancer among Tunisian Women von Zidi, Sabrina, Benothmen, Yosra, Sghaier, Ikram, Ghazoueni, Ezzeddine, Mezlini, Amel, Slimen, Bouraoui, Yacoubi-Loueslati, Besma

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Genetic Divergence in Indigenous Wild and Cultivated Rice Species of Manipur Valley von Medhabati, K., Rajiv Das, K., Rohinikumar, M., Sunitibala, H., Dikash Singh, Th

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Functional Interactions in Transcription and Splicing of Ewing’s Sarcoma von Todorova, Roumiana

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The Relationship between Polymorphisms in the Vitamin D Receptor Gene and Bone Mineral Density in Postmenopausal Women von Moran, Jose M., Rodriguez-Velasco, Francisco J., Roncero-Martin, Raul, Rey-Sanchez, Purificación, Martinez, Mariana, Pedrera-Zamorano, Juan D.

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Construction of Genetic Linkage Map and QTL Analysis of Sink-Size Traits in Pearl Millet (Pennisetum glaucum) von Vengadessan, V., Rai, K. N., Kannan Bapu, J. R., Hash, C. T., Bhattacharjee, R., Senthilvel, S., Vinayan, M. T., Nepolean, T.

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Detection of Fetal Aneuploidies by QF-PCR in Transcervical Cell Samples von Cioni, Riccardo, Bussani, Cecilia, Di Tommaso, Mariarosaria

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Mutation Screening of Elongation Factor 2 in Shwachman-Diamond Syndrome Patients Lacking Mutations in the SBDS Gene von Nicolis, Elena, Cipolli, Marco

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Identification of a Novel Ryanodine Receptor Mutation Causing Malignant Hyperthermia von Valaskova, Iveta, Dudova, Silvie, Necasova, Jana, Ostadalova, Edita, Vanaskova, Martina, Stepankova, Dagmar, Schröderova, Ivana, Gaillyova, Renata, Kuglik, Petr

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Analysis of CYP2D6 Allele Frequencies and Identification of Novel SNPs and Sequence Variations in Sardinians von Falzoi, Matteo, Pira, Luigi, Lazzari, Paolo, Pani, Luca

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Perspectives for the Use of Quantitative Genetics in Breeding of Autogamous Plants von Ramalho, Magno Antonio Patto, Carvalho, Bruna Line, Nunes, José Airton Rodrigues

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Molecular and Chromosomal Markers for Evolutionary Considerations in Torpediniformes (Chondrichthyes, Batoidea) von Rocco, Lucia

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Fetal Nucleic Acids in Maternal Circulation: A Genetic Resource for Noninvasive Prenatal Diagnosis von Banerjee, Monisha, Misra, Deepika

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No Association of Leptin Receptor Gene Gln223Arg Polymorphism with Capillary Glucose Levels: A Preliminary Population Base Cross-Sectional Study von Pena, Geórgia das Graças, Guimarães, Andre Luiz Sena, Veloso, Rosângela Ramos, Reis, Tatiana Carvalho, Neto, João Felício Rodrigues, Velasquez-Melendez, Gustavo

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Hypermethylation of INS Promoter in the Developing Liver of Cattle von Lisowski, Pawel, Flisikowski, Krzysztof, Zwierzchowski, Lech

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Genotyping of CYP2D6 Polymorphisms by MALDI-TOF Mass Spectrometry in Sardinian People von Falzoi, Matteo, Pira, Luigi, Lazzari, Paolo, Pani, Luca

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Study Designs in Genetic Epidemiology von Sahebi, Leyla, Dastgiri, Saeed, Ansarin, Khalil, Sahebi, Roya, Mohammadi, Seyyed Abolghasem

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Cuban Adolescents Requesting Presymptomatic Testing for Spinocerebellar Ataxia Type 2 von Cruz-Mariño, Tania, Velázquez-Pérez, Luis, González-Zaldivar, Yanetza, Aguilera-Rodríguez, Raúl, Velázquez-Santos, Miguel, Vázquez-Mojena, Yaimé, Estupiñán-Rodríguez, Annelié, Laffita-Mesa, José Miguel, Reynaldo-Armiñán, Rubén, Almaguer-Mederos, Luis Enrique, Paneque, Milena

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Reference Analysis in a Misclassification Model for the Meiosis I Nondisjunction Fraction in Trisomies von Loschi, Rosangela H., Mayrink, Vinicius D.

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Assessment of CYP2C9, CYP2C19, and CYP2D6 Polymorphisms in Allergic Patients with Chemical Sensitivity von D’Attis, Simona, Massari, Serafina, Mazzei, Francesca, Maio, Dominga, Vergallo, Ilaria, Mauro, Salvatore, Minelli, Mauro, Bozzetti, Maria Pia

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Case-only exome variation analysis of severe alcohol dependence using a multivariate hierarchical gene clustering approach von Gentry, Amanda Elswick, Alexander, Jeffry C, Ahangari, Mohammad, Peterson, Roseann E, Miles, Michael F, Bettinger, Jill C, Davies, Andrew G, Groteweil, Mike, Bacanu, Silviu A, Kendler, Kenneth S, Riley, Brien P, Webb, Bradley T

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