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There are 33708 results for: content related to: Polymorphic variants at 10q25.3 and 17q22 loci and the risk of non-syndromic cleft lip and palate in the polish population

  1. Resequencing of VAX1 in patients with nonsyndromic cleft lip with or without cleft palate

    Birth Defects Research Part A: Clinical and Molecular Teratology

    Volume 94, Issue 11, November 2012, Pages: 925–933, Entessar Nasser, Elisabeth Mangold, Daniela C. Tradowsky, Heide Fier, Jessica Becker, Anne C. Boehmer, Ruth Herberz, Nadine Fricker, Sandra Barth, Philipp Wahle, Stefanie Nowak, Heiko Reutter, Rudolf H. Reich, Carola Lauster, Bert Braumann, Thomas Kreusch, Alexander Hemprich, Bernd Pötzsch, Per Hoffmann, Franz-Josef Kramer, Michael Knapp, Christoph Lange, Markus M. Nöthen and Kerstin U. Ludwig

    Version of Record online : 18 OCT 2012, DOI: 10.1002/bdra.23078

  2. Genetic risk factors for nonsyndromic cleft lip with or without cleft palate in a Brazilian population with high African ancestry

    American Journal of Medical Genetics Part A

    Volume 167, Issue 10, October 2015, Pages: 2344–2349, Andrea do Rego Borges, Jamile Sá, Ryuichi Hoshi, Camila Sane Viena, Lorena C. Mariano, Patricia de Castro Veiga, Alena Peixoto Medrado, Renato Assis Machado, Sibele Nascimento de Aquino, Ana Camila Messetti, Richard A. Spritz, Ricardo D. Coletta and Silvia R. A. Reis

    Version of Record online : 22 JUL 2015, DOI: 10.1002/ajmg.a.37181

  3. 10q25.3 (DMBT1) copy number changes in astrocytoma grades II and IV

    Genes, Chromosomes and Cancer

    Volume 39, Issue 1, January 2004, Pages: 22–28, Peter H. Wessels, Albert Twijnstra, Bela Kubat, Monique I.J. Ummelen, Sandra M.H. Claessen, Raf Sciot, Adrian Merlo, Frans C.S. Ramaekers, Ernst J.M. Speel and Anton H.N. Hopman

    Version of Record online : 7 OCT 2003, DOI: 10.1002/gcc.10288

  4. Chromosome 10

    Standard Article

    eLS

    Theologia Sarafidou and Nicholas Moschonas

    Published Online : 6 MAR 2017, DOI: 10.1002/9780470015902.a0005819.pub3

  5. You have free access to this content
    The Human Obesity Gene Map: The 2004 Update

    Obesity Research

    Volume 13, Issue 3, March 2005, Pages: 381–490, Louis Pérusse, Tuomo Rankinen, Aamir Zuberi, Yvon C. Chagnon, S. John Weisnagel, George Argyropoulos, Brandon Walts, Eric E. Snyder and Claude Bouchard

    Version of Record online : 6 SEP 2012, DOI: 10.1038/oby.2005.50

  6. You have free access to this content
    The Human Obesity Gene Map: The 2005 Update

    Obesity

    Volume 14, Issue 4, April 2006, Pages: 529–644, Tuomo Rankinen, Aamir Zuberi, Yvon C. Chagnon, S. John Weisnagel, George Argyropoulos, Brandon Walts, Louis Pérusse and Claude Bouchard

    Version of Record online : 6 SEP 2012, DOI: 10.1038/oby.2006.71

  7. Nonsyndromic cleft lip with or without cleft palate in arab populations: Genetic analysis of 15 risk loci in a novel case–control sample recruited in Yemen

    Birth Defects Research Part A: Clinical and Molecular Teratology

    Volume 100, Issue 4, April 2014, Pages: 307–313, Khalid Ahmed Aldhorae, Anne C. Böhmer, Kerstin U. Ludwig, Ahlam Hibatulla Ali Esmail, Nezar Noor Al-Hebshi, Bärbel Lippke, Lina Gölz, Markus M. Nöthen, Nikolaos Daratsianos, Michael Knapp, Andreas Jäger and Elisabeth Mangold

    Version of Record online : 13 MAR 2014, DOI: 10.1002/bdra.23221

  8. Persistence of müllerian duct structures in a genetic male with distal monosomy 10q

    American Journal of Medical Genetics Part A

    Volume 167, Issue 4, April 2015, Pages: 791–796, Mustafa Tosur, Cara A. Geary, Reuben Matalon, Ravi S. Radhakrishnan, Leonard E. Swischuk, William F. Tarry, Jianli Dong and Phillip D. K. Lee

    Version of Record online : 29 MAR 2015, DOI: 10.1002/ajmg.a.37014

  9. Genetic risk factors for nonsyndromic cleft lip with or without cleft palate in a Mesoamerican population: Evidence for IRF6 and variants at 8q24 and 10q25

    Birth Defects Research Part A: Clinical and Molecular Teratology

    Volume 88, Issue 7, July 2010, Pages: 535–537, Augusto Rojas-Martinez, Heiko Reutter, Oscar Chacon-Camacho, Rafael B. R. Leon-Cachon, Sergio G. Munoz-Jimenez, Stefanie Nowak, Jessica Becker, Ruth Herberz, Kerstin U. Ludwig, Mario Paredes-Zenteno, Abelardo Arizpe-Cantú, Susanne Raeder, Stefan Herms, Rocio Ortiz-Lopez, Michael Knapp, Per Hoffmann, Markus M. Nöthen and Elisabeth Mangold

    Version of Record online : 17 JUN 2010, DOI: 10.1002/bdra.20689

  10. You have free access to this content
    The Human Obesity Gene Map: The 2003 Update

    Obesity Research

    Volume 12, Issue 3, March 2004, Pages: 369–439, Eric E. Snyder, Brandon Walts, Louis Pérusse, Yvon C. Chagnon, S. John Weisnagel, Tuomo Rankinen and Claude Bouchard

    Version of Record online : 6 SEP 2012, DOI: 10.1038/oby.2004.47

  11. Analysis of genomewide association signals for nonsyndromic cleft lip/palate in a Kenya African cohort

    American Journal of Medical Genetics Part A

    Volume 155, Issue 10, October 2011, Pages: 2422–2425, R. Christopher Weatherley-White, Songtao Ben, Ying Jin, Sheri Riccardi, Thomas D. Arnold and Richard A. Spritz

    Version of Record online : 16 AUG 2011, DOI: 10.1002/ajmg.a.34191

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    10q26.1 Microdeletion: Redefining the critical regions for microcephaly and genital anomalies

    American Journal of Medical Genetics Part A

    Volume 167, Issue 11, November 2015, Pages: 2707–2713, Nancy Choucair, Joelle Abou Ghoch, Ali Fawaz, André Mégarbané and Eliane Chouery

    Version of Record online : 26 JUN 2015, DOI: 10.1002/ajmg.a.37211

  13. Chromosome 10q24.3-qter deletion associated with left-sided first branchial arch defect, diaphragmatic eventration, and duplicated renal pelvis

    American Journal of Medical Genetics Part A

    Volume 140A, Issue 20, 15 October 2006, Pages: 2241–2244, Jia-Woei Hou

    Version of Record online : 12 SEP 2006, DOI: 10.1002/ajmg.a.31429

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    Deletion Variants of RABGAP1L, 10q21.3, and C4 Are Associated With the Risk of Systemic Lupus Erythematosus in Korean Women

    Arthritis & Rheumatism

    Volume 65, Issue 4, April 2013, Pages: 1055–1063, Ji-Hong Kim, Seung-Huyn Jung, Joon Seol Bae, Hye-Soon Lee, Seon-Hee Yim, So-Yeon Park, So-Young Bang, Hae-Jin Hu, Hyoung Doo Shin, Sang-Cheol Bae and Yeun-Jun Chung

    Version of Record online : 28 MAR 2013, DOI: 10.1002/art.37854

  15. Human-Mouse Comparative Maps

    Appendix

    Current Protocols in Human Genetics

    6:A.6.1–A.6.42

    Michael F. Seldin

    Published Online : 1 MAY 2001, DOI: 10.1002/0471142905.hga06s09

  16. Clinical comparison of 10q26 overlapping deletions: Delineating the critical region for urogenital anomalies

    American Journal of Medical Genetics Part A

    Volume 167, Issue 4, April 2015, Pages: 786–790, Ascensión Vera-Carbonell, Vanesa López-González, Juan Antonio Bafalliu, María J Ballesta-Martínez, Asunción Fernández, Encarna Guillén-Navarro and Isabel López-Expósito

    Version of Record online : 5 FEB 2015, DOI: 10.1002/ajmg.a.36949

  17. Interstitial deletion del(10)(q25.2q25.3 ∼ 26.11)—case report and review of the literature

    Prenatal Diagnosis

    Volume 25, Issue 10, October 2005, Pages: 954–959, Hildegard Kehrer-Sawatzki, Eva Daumiller, Jutta Müller-Navia, Heidemarie Kendziorra, Eva Rossier, Gabriele du Bois and Gotthold Barbi

    Version of Record online : 8 AUG 2005, DOI: 10.1002/pd.1252

  18. Association between polymorphisms at the GREM1 locus and the risk of nonsyndromic cleft lip with or without cleft palate in the Polish population

    Birth Defects Research Part A: Clinical and Molecular Teratology

    Volume 103, Issue 10, October 2015, Pages: 847–856, Adrianna Mostowska, Kamil K. Hozyasz, Piotr Wójcicki, Kacper Żukowski, Anna Dąbrowska, Agnieszka Lasota, Małgorzata Zadurska, Agnieszka Radomska, Izabela Dunin-Wilczyńska and Paweł P. Jagodziński

    Version of Record online : 4 JUN 2015, DOI: 10.1002/bdra.23391

  19. Prenatal diagnosis and molecular cytogenetic analysis of partial monosomy 10q (10q25.3[RIGHTWARDS ARROW]qter) and partial trisomy 18q (18q23[RIGHTWARDS ARROW]qter) in a fetus associated with cystic hygroma and ambiguous genitalia

    Prenatal Diagnosis

    Volume 25, Issue 6, June 2005, Pages: 492–496, Chih-Ping Chen, Schu-Rern Chern, Tzu-Hao Wang, Ding-Wei Hsueh, Chen-Chi Lee, Dai-Dyi Town, Wayseen Wang and Tsang-Ming Ko

    Version of Record online : 20 JUN 2005, DOI: 10.1002/pd.1179

  20. Risks of unbalanced progeny at amniocentesis to carriers of chromosome rearrangements: Data from United States and Canadian laboratories

    American Journal of Medical Genetics

    Volume 33, Issue 1, May 1989, Pages: 14–53, Dr. Art Daniel, Ernest B. Hook and Gary Wulf

    Version of Record online : 5 JUN 2005, DOI: 10.1002/ajmg.1320330105