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There are 69933 results for: content related to: Subtelomeric deletion of chromosome 10p15.3: Clinical findings and molecular cytogenetic characterization

  1. Clinical description of a patient carrying the smallest reported deletion involving 10p14 region

    American Journal of Medical Genetics Part A

    Volume 158A, Issue 4, April 2012, Pages: 832–835, Daniela Melis, Rita Genesio, Pasquale Boemio, Ennio Del Giudice, Gerarda Cappuccio, Angela Mormile, Valentina Ronga, Anna Conti, Floriana Imperati, Lucio Nitsch and Generoso Andria

    Version of Record online : 9 MAR 2012, DOI: 10.1002/ajmg.a.34133

  2. Recurrent copy number variations as risk factors for autism spectrum disorders: analysis of the clinical implications

    Clinical Genetics

    Volume 89, Issue 6, June 2016, Pages: 708–718, V. Oikonomakis, K. Kosma, A. Mitrakos, C. Sofocleous, P. Pervanidou, A. Syrmou, A. Pampanos, S. Psoni, H. Fryssira, E. Kanavakis, S. Kitsiou-Tzeli and M. Tzetis

    Version of Record online : 9 FEB 2016, DOI: 10.1111/cge.12740

  3. Small supernumerary marker chromosome originating from chromosome 10 associated with an apparently normal phenotype

    American Journal of Medical Genetics Part A

    Volume 149A, Issue 12, December 2009, Pages: 2768–2774, Pi-Lin Sung, Sheng-Ping Chang, Kuo-Chang Wen, Chia-Ming Chang, Ming-Jie Yang, Lin-Chao Chen, Kuan-Chong Chao, Chi-Ying F. Huang, Yueh-Chun Li and Chyi-Chyang Lin

    Version of Record online : 16 NOV 2009, DOI: 10.1002/ajmg.a.32878

  4. Severe clinical presentation in monozygotic twins with 10p15.3 microdeletion syndrome

    American Journal of Medical Genetics Part A

    Volume 164, Issue 3, March 2014, Pages: 764–768, Euthymia Vargiami, Athina Ververi, Maria Kyriazi, Evangelia Papathanasiou, Georgia Gioula, Spyridon Gerou, Hamda Al-Mutawa, Marios Kambouris and Dimitrios I. Zafeiriou

    Version of Record online : 19 DEC 2013, DOI: 10.1002/ajmg.a.36329

  5. Interstitial deletion of 10p and atrial septal defect in DiGeorge 2 syndrome

    Clinical Genetics

    Volume 66, Issue 2, August 2004, Pages: 128–136, SA Yatsenko, AN Yatsenko, K Szigeti, WJ Craigen, P Stankiewicz, SW Cheung and JR Lupski

    Version of Record online : 25 JUN 2004, DOI: 10.1111/j.1399-0004.2004.00290.x

  6. 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

  7. Unrelated chromosomal anomalies found in patients with suspected 22q11.2 deletion

    American Journal of Medical Genetics Part A

    Volume 146A, Issue 9, 1 May 2008, Pages: 1134–1141, Luis Fernández, Pablo Lapunzina, Isidora López Pajares, María Palomares, Isabel Martínez, Blanca Fernández, José Quero, Luis García-Guereta, Alfredo García-Alix, Margarita Burgueros, Enrique Galán-Gómez, José María Carbonell-Pérez, Ángeles Pérez-Granero, Laura Torres-Juan, Damià Heine-Suñer, Jordi Rosell and Alicia Delicado

    Version of Record online : 2 APR 2008, DOI: 10.1002/ajmg.a.32256

  8. Cleft palate in a multigenerational family with a microdeletion of 20p12.3 involving BMP2

    American Journal of Medical Genetics Part A

    Volume 158A, Issue 10, October 2012, Pages: 2616–2620, Eli S. Williams, Kim A. Uhas, Brian P. Bunke, Kathryn B. Garber and Christa L. Martin

    Version of Record online : 10 SEP 2012, DOI: 10.1002/ajmg.a.35594

  9. First reported case of interstitial 15 q15.3-q21.3 deletion diagnosed prenatally and characterized with array CGH in a fetus with an isolated short femur

    American Journal of Medical Genetics Part A

    Volume 158A, Issue 3, March 2012, Pages: 617–621, Fatma Abdelhedi, Johanna Corcos, Laurence Cuisset, Vassilis Tsatsaris, Julia Tantau, Dominique Le Tessier, Aziza Lebbar and Jean-Michel Dupont

    Version of Record online : 2 FEB 2012, DOI: 10.1002/ajmg.a.34416

  10. Interstitial 10p11.23–p12.1 microdeletions associated with developmental delay, craniofacial abnormalities, and cryptorchidism

    American Journal of Medical Genetics Part A

    Volume 164, Issue 10, October 2014, Pages: 2623–2626, Henry J. Mroczkowski, Georgianne Arnold, Francis X. Schneck, Aleksandar Rajkovic and Svetlana A. Yatsenko

    Version of Record online : 29 JUL 2014, DOI: 10.1002/ajmg.a.36627

  11. Evidence for the multigenic inheritance of schizophrenia

    American Journal of Medical Genetics

    Volume 105, Issue 8, 8 December 2001, Pages: 794–800, Robert Freedman, Sherry Leonard, Ann Olincy, Charles A. Kaufmann, Dolores Malaspina, C. Robert Cloninger, Dragan Svrakic, Stephen V. Faraone and Ming T. Tsuang

    Version of Record online : 29 OCT 2001, DOI: 10.1002/ajmg.10100

  12. Is the disruption of an N-myristoyltransferase (NMT2) associated with hypoplastic testes?

    American Journal of Medical Genetics Part A

    Volume 143A, Issue 15, 1 August 2007, Pages: 1796–1798, Fabiola Quintero-Rivera, Natalia T. Leach, Albert de la Chapelle, James F. Gusella, Cynthia C. Morton and David J. Harris

    Version of Record online : 13 JUN 2007, DOI: 10.1002/ajmg.a.31799

  13. Microdeletion 20p12.3 involving BMP2 contributes to syndromic forms of cleft palate

    American Journal of Medical Genetics Part A

    Volume 155, Issue 7, July 2011, Pages: 1646–1653, Trilochan Sahoo, Aaron Theisen, Pedro A. Sanchez-Lara, Michael Marble, Daniela N. Schweitzer, Beth S. Torchia, Allen N. Lamb, Bassem A. Bejjani, Lisa G. Shaffer and Yves Lacassie

    Version of Record online : 10 JUN 2011, DOI: 10.1002/ajmg.a.34063

  14. You have free access to this content
    Identification of a Major Locus for Paget's Disease on Chromosome 10p13 in Families of British Descent

    Journal of Bone and Mineral Research

    Volume 23, Issue 1, January 2008, Pages: 58–63, Gavin JA Lucas, Phillip L Riches, Lynne J Hocking, Tim Cundy, Geoff C Nicholson, John P Walsh and Stuart H Ralston

    Version of Record online : 1 OCT 2007, DOI: 10.1359/jbmr.071004

  15. Early genetic events in HPV immortalised keratinocytes

    Genes, Chromosomes and Cancer

    Volume 30, Issue 1, January 2001, Pages: 72–79, Amanda Cottage, Sally Dowen, Ian Roberts, Mark Pett, Nicholas Coleman and Margaret Stanley

    Version of Record online : 27 SEP 2000, DOI: 10.1002/1098-2264(2000)9999:9999<::AID-GCC1060>3.0.CO;2-X

  16. Germline duplication of chromosomes 10p15.3 and Yp11.32 in a man with learning disability and early onset cutaneous malignant melanoma

    American Journal of Medical Genetics Part A

    Volume 146A, Issue 17, 1 September 2008, Pages: 2298–2300, Ercan Mihci and Noralane M. Lindor

    Version of Record online : 31 JUL 2008, DOI: 10.1002/ajmg.a.32442

  17. Co-occurrence of 22q11 deletion syndrome and hdr syndrome

    American Journal of Medical Genetics Part A

    Volume 161, Issue 10, October 2013, Pages: 2576–2581, Ryoko Fukai, Nobuhiko Ochi, Akira Murakami, Mitsuko Nakashima, Yoshinori Tsurusaki, Hirotomo Saitsu, Naomichi Matsumoto and Noriko Miyake

    Version of Record online : 5 AUG 2013, DOI: 10.1002/ajmg.a.36083

  18. Alteration of enhancer of polycomb 1 at 10p11.2 is one of the genetic events leading to development of adult T-cell leukemia/lymphoma

    Genes, Chromosomes and Cancer

    Volume 48, Issue 9, September 2009, Pages: 768–776, Shingo Nakahata, Yusuke Saito, Makoto Hamasaki, Tomonori Hidaka, Yasuhito Arai, Tomohiko Taki, Masafumi Taniwaki and Kazuhiro Morishita

    Version of Record online : 29 MAY 2009, DOI: 10.1002/gcc.20681

  19. Association analysis of the PIP4K2A gene on chromosome 10p12 and schizophrenia in the Irish study of high density schizophrenia families (ISHDSF) and the Irish case–control study of schizophrenia (ICCSS)

    American Journal of Medical Genetics Part B: Neuropsychiatric Genetics

    Volume 153B, Issue 1, January 2010, Pages: 323–331, D.L. Thiselton, B.S. Maher, B.T. Webb, T.B. Bigdeli, F.A. O'Neill, D. Walsh, K.S. Kendler and B.P. Riley

    Version of Record online : 27 MAY 2009, DOI: 10.1002/ajmg.b.30982

  20. Identification of genomic changes associated with cisplatin resistance in testicular germ cell tumor cell lines

    Genes, Chromosomes and Cancer

    Volume 47, Issue 7, July 2008, Pages: 604–613, Elodie E. Noel, Jackie Perry, Tracy Chaplin, Xueying Mao, Jean-Baptiste Cazier, Simon P. Joel, R. Tim D. Oliver, Bryan D. Young and Yong-Jie Lu

    Version of Record online : 2 APR 2008, DOI: 10.1002/gcc.20564