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Genetics of congenital heart disease: the contribution of the noncoding regulatory genome de réir Alex V. Postma, Connie R. Bezzina, Vincent M. Christoffels

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Bardet–Biedl syndrome: Is it only cilia dysfunction? de réir Rossina Novas, Magdalena Cárdenas-Rodríguez, Florencia Irigoı́n, José L. Badano

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Whole Exome Sequencing Reveals Mutations in Known Retinal Disease Genes in 33 out of 68 Israeli Families with Inherited Retinopathies de réir Avigail Beryozkin, Elia Shevah, Adva Kimchi, Liliana Mizrahi‐Meissonnier, Samer Khateb, Rinki Ratnapriya, Csilla H. Lazar, Anat Blumenfeld, Tamar Ben‐Yosef, Yitzhak Hemo, Jacob Pe’er, Eduard Averbuch, Michal Sagi, Alexis Boleda, Linn Gieser, Abraham Zlotogorski, Tzipora C. Falik‐Zaccai, Ola Alimi-Kasem, Samuel G. Jacobson, Itay Chowers, Anand Swaroop, Eyal Banin, Dror Sharon

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Inherited Cardiomyopathies de réir Polakit Teekakirikul, Melissa Kelly, Heidi L. Rehm, Neal K. Lakdawala, Birgit H. Funke

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STAG3 truncating variant as the cause of primary ovarian insufficiency de réir Polona Le Quesne Stabej, Hywel Williams, Chela James, Mehmet Tekman, Horia Stanescu, Robert Kleta, Louise Ocaka, Francesco Lescai, Helen L. Storr, Maria Bitner‐Glindzicz, Chiara Bacchelli, Gerard S. Conway

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Harnessing Pandemonium: The Clinical Implications of Tumor Heterogeneity in Ovarian Cancer de réir Sarah P. Blagden

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Multicenter Linkage Study of Schizophrenia Candidate Regions on Chromosomes 5q, 6q, 10p, and 13q: Schizophrenia Linkage Collaborative Group III de réir Douglas F. Levinson, Peter Holmans, Richard E. Straub, Michael J. Owen, Dieter B. Wildenauer, Pablo V. Gejman, Ann E. Pulver, Claudine Laurent, Kenneth S. Kendler, Dermot Walsh, Nadine Norton, Nigel Williams, Sibylle G. Schwab, Bernard Lerer, Bryan Mowry, Alan R. Sanders, Stylianos E. Antonarakis, Jean-Louis Blouin, Jean‐François Deleuze, Jacques Mallet

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Genetics of cleft lip and cleft palate de réir Elizabeth J. Leslie, Mary L. Marazita

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Advances in genetic therapeutic strategies for Duchenne muscular dystrophy de réir Simon Guiraud, Huijia Chen, D T Burns, Kay E. Davies

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<i>NCAM1‐TTC12‐ANKK1‐DRD2</i> gene cluster and the clinical and genetic heterogeneity of adults with ADHD de réir Nina Roth Mota, Diego Luiz Rovaris, Djenifer B. Kappel, Felipe Almeida Picon, Eduardo S. Vitola, Carlos Alberto Iglesias Salgado, Rafael G. Karam, Luís Augusto Rohde, Eugênio H. Grevet, Claiton Henrique Dotto Bau

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Charcot‐Marie‐Tooth Disease: A Clinico‐genetic Confrontation de réir Nina Barišić, Kristl G. Claeys, Maja Sirotković-Skerlev, A. Löfgren, Eva Nelis, Peter De Jonghe, Vincent Timmerman

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Genes and mutations causing retinitis pigmentosa de réir Stephen P. Daiger, L.S. Sullivan, S. J. Bowne

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Mutations in human IFT140 cause non-syndromic retinal degeneration de réir Mingchu Xu, Lizhu Yang, Feng Wang, Huajin Li, Xia Wang, Weichen Wang, Zhongqi Ge, Keqing Wang, Li Zhao, Hui Li, Yumei Li, Ruifang Sui, Rui Chen

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Genomic and epigenomic heterogeneity in chronic lymphocytic leukemia de réir Romain Guièze, Catherine J. Wu

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Identification of embryonic lethal genes in humans by autozygosity mapping and exome sequencing in consanguineous families de réir Hanan E. Shamseldin, Maha Tulbah, Wesam Kurdi, Maha Nemer, Nada Alsahan, Elham Al Mardawi, Ola Khalifa, Amal Hashem, Ahmed M Kurdi, Zainab Babay, Dalal Bubshait, Niema Ibrahim, Firdous Abdulwahab, Zuhair Rahbeeni, Mais Hashem, Fowzan S. Alkuraya

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Genetics of rheumatoid arthritis: confronting complexity. de réir Peter K. Gregersen

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Next-generation sequencing applied to a large French cone and cone-rod dystrophy cohort: mutation spectrum and new genotype-phenotype correlation de réir Élise Boulanger-Scemama, Saïd El Shamieh, Vanessa Démontant, Christel Condroyer, Aline Antonio, Christelle Michiels, Fiona Boyard, Jean‐Paul Saraiva, Mélanie Letexier, Eric H. Souied, Saddek Mohand‐Saïd, José‐Alain Sahel, Christina Zeitz, Isabelle Audo

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Mutations in a new photoreceptor-pineal gene on 17p cause Leber congenital amaurosis de réir Melanie M. Sohocki, Sara J. Bowne, Lori S. Sullivan, Seth Blackshaw, Constance L. Cepko, Annette Payne, Shomi Bhattacharya, Shagufta Khaliq, S. Qasim Mehdi, David G. Birch, Wilbur R. Harrison, F.F.B. Elder, John R. Heckenlively, Stephen P. Daiger

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Cognitive heterogeneity in schizophrenia de réir Eileen M. Joyce, Jonathan P. Roiser

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‘Genetic heterogeneity' in HER2/neu testing by fluorescence in situ hybridization: a study of 2522 cases de réir Martin C. Chang, Janet I. Malowany, Julita Mazurkiewicz, Martha Wood

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