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There are 348502 results for: content related to: Meiotic exchange event within the stalk region of an inverted chromosome 22 results in a recombinant chromosome with duplication of the distal long arm

  1. Prenatal diagnosis of an unexpected interstitial 22q11.2 deletion causing truncus arteriosus and thymic hypoplasia in a ring 22 chromosome derived from a maternally inherited paracentric inversion

    Prenatal Diagnosis

    Volume 26, Issue 13, December 2006, Pages: 1212–1215, Jennifer McClarren, Alan E. Donnenfeld and J. Britt Ravnan

    Version of Record online : 13 NOV 2006, DOI: 10.1002/pd.1590

  2. Familial transmission of a deletion of chromosome 21 derived from a translocation between chromosome 21 and an inverted chromosome 22

    American Journal of Medical Genetics

    Volume 70, Issue 4, 27 June 1997, Pages: 399–403, Hana Aviv, Caroline Lieber, Aswani Yenamandra and Franklin Desposito

    Version of Record online : 6 DEC 1998, DOI: 10.1002/(SICI)1096-8628(19970627)70:4<399::AID-AJMG12>3.0.CO;2-C

  3. Ring chromosome 22 and neurofibromatosis type II: proof of two-hit model for the loss of the NF2 gene in the development of meningioma

    Clinical Genetics

    Volume 81, Issue 1, January 2012, Pages: 82–87, B Zirn, L Arning, I Bartels, M Shoukier, S Hoffjan, B Neubauer and A Hahn

    Version of Record online : 22 DEC 2010, DOI: 10.1111/j.1399-0004.2010.01598.x

  4. Does chromosome 22 have anything to do with sex determination: Further studies on a 46,XX,22q11.2 del male

    American Journal of Medical Genetics Part A

    Volume 123A, Issue 1, November 15, 2003, Pages: 64–67, Robert P. Erickson, Steve Skinner, Hélène Jacquet, Dominique Campion, Patrick G. Buckley, Kiran K. Mantripragada and Jan P. Dumanski

    Version of Record online : 26 AUG 2003, DOI: 10.1002/ajmg.a.20489

  5. 22q13 deletion syndrome

    American Journal of Medical Genetics

    Volume 101, Issue 2, 15 June 2001, Pages: 91–99, Mary C. Phelan, R. Curtis Rogers, Robert A. Saul, Gail A. Stapleton, Kevin Sweet, Heather McDermid, Steven R. Shaw, Joanne Claytor, Jan Willis and Desmond P. Kelly

    Version of Record online : 29 MAY 2001, DOI: 10.1002/1096-8628(20010615)101:2<91::AID-AJMG1340>3.0.CO;2-C

  6. Partial trisomy of chromosome 22 resulting from a supernumerary marker chromosome 22 in a child with features of cat eye syndrome

    American Journal of Medical Genetics Part A

    Volume 146A, Issue 14, 15 July 2008, Pages: 1871–1874, Valérie Bélien, Marion Gérard-Blanluet, Stéphane Serero, Nathalie Le Dû, Clarisse Baumann, Marie-Line Jacquemont, Céline Dupont, Kada Krabchi, Séverine Drunat, Annie Elbez, Jean-Claude Janaud, Brigitte Benzacken, Alain Verloes, Anne-Claude Tabet and Azzedine Aboura

    Version of Record online : 13 JUN 2008, DOI: 10.1002/ajmg.a.32392

  7. You have free access to this content
    Molecular cytogenetic characterization of a recombinant chromosome rec(22)dup(22q)inv(22)(p13q12.2)

    American Journal of Medical Genetics Part A

    Volume 124A, Issue 1, 1 January 2004, Pages: 92–95, Vijay S. Tonk, C.A. Jesurun, David L. Morgan, Lillian H. Lockhart and Gopalrao V.N. Velagaleti

    Version of Record online : 15 SEP 2003, DOI: 10.1002/ajmg.a.20384

  8. Narrowing the critical region for a rhabdoid tumor locus in 22q11

    Genes, Chromosomes and Cancer

    Volume 16, Issue 2, June 1996, Pages: 94–105, Jaclyn A. Biegel, Cindy S. Allen, Kazuhiko Kawasaki, Nobuyoshi Shimizu, Marcia L. Budarf and Callum J. Bell

    Version of Record online : 7 DEC 1998, DOI: 10.1002/(SICI)1098-2264(199606)16:2<94::AID-GCC3>3.0.CO;2-Y

  9. Parental origin of the extra chromosome in the cat eye syndrome: Evidence from heteromorphism and in situ hybridization analysis

    American Journal of Medical Genetics

    Volume 29, Issue 1, January 1988, Pages: 9–19, Dr. R. E. Magenis, R. R. Sheehy, M. G. Brown, H. E. McDermid, B. N. White, J. Zonana, R. Weleber, John M. Optiz and James F. Reynolds

    Version of Record online : 4 JUN 2005, DOI: 10.1002/ajmg.1320290103

  10. Male pseudohermaphroditism and gonadal mosaicism in a 47,XY,+22 fetus

    American Journal of Medical Genetics Part A

    Volume 140A, Issue 16, 15 August 2006, Pages: 1768–1772, Mélanie Beaulieu Bergeron, Danh Tran-Thanh, Jean-Christophe Fournet, Emmanuelle Lemyre, Nicole Lemieux and Dorothée Bouron-Dal Soglio

    Version of Record online : 11 JUL 2006, DOI: 10.1002/ajmg.a.31338

  11. No evidence for linkage of chromosome 22 markers to schizophrenia in Southern African Bantu-speaking families

    American Journal of Medical Genetics

    Volume 67, Issue 6, 22 November 1996, Pages: 515–522, Brien Riley, Mphala Mogudi-Carter, Trefor Jenkins and Robert Williamson

    Version of Record online : 6 DEC 1998, DOI: 10.1002/(SICI)1096-8628(19961122)67:6<515::AID-AJMG2>3.0.CO;2-G

  12. You have free access to this content
    Isochromosome 22 in trisomy 22 mosaic with five cell lines

    American Journal of Medical Genetics Part A

    Volume 124A, Issue 1, 1 January 2004, Pages: 79–84, Carol Guzé, Naigeng Qin, JoAnn Kelly, Xiaojing Yang, Roberta Bruni, Debra Baker and Rosetta Hassan

    Version of Record online : 16 JUL 2003, DOI: 10.1002/ajmg.a.20365

  13. Genomic analysis of chromosome 22 in synchronous and histologically distinct intracranial tumours in a child

    Neuropathology and Applied Neurobiology

    Volume 36, Issue 4, June 2010, Pages: 359–363, U. Pohl, A. F. Dean, K. Ichimura, L. Liu, J. Nicholson, J. Cross and V. P. Collins

    Version of Record online : 22 MAR 2010, DOI: 10.1111/j.1365-2990.2010.01085.x

  14. Detailed analysis of 22q11.2 with a high density MLPA probe set

    Human Mutation

    Volume 29, Issue 3, March 2008, Pages: 433–440, G.R. Jalali, J.A.S. Vorstman, Ab Errami, R. Vijzelaar, J. Biegel, T. Shaikh and B.S. Emanuel

    Version of Record online : 21 NOV 2007, DOI: 10.1002/humu.20640

  15. A 7 Mb duplication at 22q13 in a girl with bipolar disorder and hippocampal malformation

    American Journal of Medical Genetics Part A

    Volume 146A, Issue 13, 1 July 2008, Pages: 1754–1760, Tiziano Pramparo, Manuela de Gregori, Stefania Gimelli, Roberto Ciccone, Domenico Frondizi, Thomas Liehr, Simona Pellacani, Gabriele Masi, Paola Brovedani, Orsetta Zuffardi and Renzo Guerrini

    Version of Record online : 10 JUN 2008, DOI: 10.1002/ajmg.a.32326

  16. Ring chromosome 22 and autism: Report and review

    American Journal of Medical Genetics

    Volume 90, Issue 5, 28 February 2000, Pages: 382–385, Joanna E. MacLean, Ikuko E. Teshima, Peter Szatmari and Małgorzata J.M. Nowaczyk

    Version of Record online : 23 MAR 2000, DOI: 10.1002/(SICI)1096-8628(20000228)90:5<382::AID-AJMG7>3.0.CO;2-T

  17. Philadelphia-negative chronic myeloid leukaemia: detection by FISH of BCR-ABL fusion gene localized either to chromosome 9 or chromosome 22

    British Journal of Haematology

    Volume 87, Issue 2, June 1994, Pages: 409–412, E. Nacheva, T. Holloway, K. Brown, D. Bloxham and A. R. Green

    Version of Record online : 12 MAR 2008, DOI: 10.1111/j.1365-2141.1994.tb04933.x

  18. Cytogenetic and molecular analysis of a t(1;22)(p36;q11.2) in a rhabdoid tumor with a putative homozygous deletion of chromosome 22

    Genes, Chromosomes and Cancer

    Volume 21, Issue 2, February 1998, Pages: 82–89, Christophe Rosty, Martine Peter, Jessica Zucman, Pierre Validire, Olivier Delattre and Alain Aurias

    Version of Record online : 7 DEC 1998, DOI: 10.1002/(SICI)1098-2264(199802)21:2<82::AID-GCC2>3.0.CO;2-3

  19. The Molecular Genetics of Meningiomas

    Brain Pathology

    Volume 1, Issue 1, September 1990, Pages: 19–24, V. Peter Collins, Magnus Nordenskjold and Jan P. Dumanski

    Version of Record online : 28 JAN 2008, DOI: 10.1111/j.1750-3639.1990.tb00634.x

  20. NF2 status of meningiomas is associated with tumour localization and histology

    The Journal of Pathology

    Volume 194, Issue 3, July 2001, Pages: 367–372, Johan Kros, Kitty de Greve, Angela van Tilborg, Wim Hop, Herman Pieterman, Cees Avezaat, Ronald Lekanne dit Deprez and Ellen Zwarthoff

    Version of Record online : 18 MAY 2001, DOI: 10.1002/path.909