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There are 14168 results for: content related to: Autoimmune thyroid syndrome in women with Turner's syndrome—the association with karyotype

  1. Thyroid autoantibodies, Turner's syndrome and growth hormone therapy

    Acta Paediatrica

    Volume 84, Issue 1, January 1995, Pages: 63–65, S-A Ivarsson, U-B Ericsson, KO Nilsson, J Gustafsson, L Hagenäs, A Häger, C Moell, T Tuvemo, O Westphal, K Albertsson-Wikland and J Åman

    Version of Record online : 21 JAN 2008, DOI: 10.1111/j.1651-2227.1995.tb13485.x

  2. The Turner syndrome life course project: Karyotype-phenotype analyses across the lifespan

    Clinical Endocrinology

    Volume 87, Issue 5, November 2017, Pages: 532–538, Antoinette Cameron- Pimblett, Clementina La Rosa, Thomas F. J. King, Melanie C. Davies and Gerard S. Conway

    Version of Record online : 24 JUL 2017, DOI: 10.1111/cen.13394

  3. You have free access to this content
    Failed gene conversion leads to extensive end processing and chromosomal rearrangements in fission yeast

    The EMBO Journal

    Volume 28, Issue 21, November 4, 2009, Pages: 3400–3412, Helen Tinline-Purvis, Andrew P Savory, Jason K Cullen, Anoushka Davé, Jennifer Moss, Wendy L Bridge, Samuel Marguerat, Jürg Bähler, Jiannis Ragoussis, Richard Mott, Carol A Walker and Timothy C Humphrey

    Version of Record online : 1 OCT 2009, DOI: 10.1038/emboj.2009.265

  4. You have free access to this content
    Myeloid neoplasms with isolated isochromosome 17q represent a clinicopathologic entity associated with myelodysplastic/myeloproliferative features, a high risk of leukemic transformation, and wild-type TP53

    Cancer

    Volume 118, Issue 11, 1 June 2012, Pages: 2879–2888, Rashmi Kanagal-Shamanna, Carlos E. Bueso-Ramos, Bedia Barkoh, Gary Lu, Sa Wang, Guillermo Garcia-Manero, Saroj Vadhan-Raj, Daniela Hoehn, L. Jeffrey Medeiros and C. Cameron Yin

    Version of Record online : 28 OCT 2011, DOI: 10.1002/cncr.26537

  5. DNA studies of mono- and pseudodicentric isochromosomes 18q

    American Journal of Medical Genetics Part A

    Volume 127A, Issue 3, 15 June 2004, Pages: 230–233, Merete Bugge, Carsten A. Brandt and Michael B. Petersen

    Version of Record online : 5 MAR 2004, DOI: 10.1002/ajmg.a.30026

  6. Isochromosomes in acute lymphoblastic leukaemia: I(21q) is a significant finding

    Genes, Chromosomes and Cancer

    Volume 17, Issue 1, September 1996, Pages: 21–30, Mary Martineau, Roslyn Clark, Dianna M. Farrell, Jacqueline M. Hawkins, Anthony V. Moorman and Lorna M. Secker-Walker

    Version of Record online : 7 DEC 1998, DOI: 10.1002/(SICI)1098-2264(199609)17:1<21::AID-GCC4>3.0.CO;2-4

  7. Grandmaternal origin of an isochromosome 18p present in two maternal half-sisters

    American Journal of Medical Genetics

    Volume 101, Issue 1, 1 June 2001, Pages: 65–69, Jane Boyle, Karan Sangha, Fred Dill, Wendy P. Robinson and Siu-Li Yong

    Version of Record online : 27 APR 2001, DOI: 10.1002/ajmg.1295

  8. Investigation of two cases of paternal disomy 13 suggests timing of isochromosome formation and mechanisms leading to uniparental disomy

    American Journal of Medical Genetics

    Volume 82, Issue 3, 29 January 1999, Pages: 275–281, Sue Ann Berend, Gerald L. Feldman, Christopher McCaskill, Paula Czarnecki, Daniel L. Van Dyke and Lisa G. Shaffer

    Version of Record online : 29 JAN 1999, DOI: 10.1002/(SICI)1096-8628(19990129)82:3<275::AID-AJMG15>3.0.CO;2-2

  9. Turner's syndrome with X-isochromosome and Hashimoto's thyroiditis

    Clinical Endocrinology

    Volume 41, Issue 5, November 1994, Pages: 673–676, M. de Kerdanet, J. Lucas, F. Lemee and M. Lecornu

    Version of Record online : 17 MAR 2008, DOI: 10.1111/j.1365-2265.1994.tb01835.x

  10. Parental origin and mechanisms of formation of three eases of 12p tetrasomy

    Clinical Genetics

    Volume 50, Issue 1, July 1996, Pages: 41–46, Catherine Turleau, Brigitte Simon-Bouy, Estelle Austruy, Marie-Claude Grisard, Françoise Lemaire, Denise Molina-Gomes, Jean-Pierre Siffroi and Joëlle Boué

    Version of Record online : 28 JUN 2008, DOI: 10.1111/j.1399-0004.1996.tb02344.x

  11. Isochromosome 18q in a fetus with congenital megacystis, intra-uterine growth retardation and cloacal dysgenesis sequence

    Prenatal Diagnosis

    Volume 18, Issue 10, October 1998, Pages: 1068–1074, Chih-Ping Chen, Schu-Rern Chern, Chen-Chi Lee and Dai-Dyi Town

    Version of Record online : 4 MAY 1999, DOI: 10.1002/(SICI)1097-0223(1998100)18:10<1068::AID-PD384>3.0.CO;2-A

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    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. Isochromosome 18p in a mother and her child

    American Journal of Medical Genetics

    Volume 46, Issue 4, 1 June 1993, Pages: 392–393, Dr. Dvorah Abeliovich, Judith Dagan, Alina Levy, Avraham Steinberg and Joel Zlotogora

    Version of Record online : 7 JUN 2005, DOI: 10.1002/ajmg.1320460409

  14. FISH and PCR analysis of the presence of Y-chromosome sequences in a patient with Xq-isochromosome and testicular tissue

    Clinical Genetics

    Volume 55, Issue 5, May 1999, Pages: 357–362, Francisco Álvarez-Nava, María C Martínez, Sandra González, Marisol Soto, Lisbeth Borjas and Alicia Rojas

    Version of Record online : 24 DEC 2001, DOI: 10.1034/j.1399-0004.1999.550510.x

  15. Maternal isochromosome 7q and paternal isochromosome 7p in a boy with growth retardation

    American Journal of Medical Genetics

    Volume 102, Issue 2, 1 August 2001, Pages: 169–172, Dieter Kotzot, Heidrun Holland, Eberhard Keller and Ursula G. Froster

    Version of Record online : 14 JUN 2001, DOI: 10.1002/ajmg.1430

  16. FISH characterization of a dicentric Yq (p11.32) isochromosome in an azoospermic male

    American Journal of Medical Genetics Part A

    Volume 127A, Issue 3, 15 June 2004, Pages: 302–306, M. Codina-Pascual, M. Oliver-Bonet, J. Navarro, H. Starke, T. Liehr, C. Gutiérrez-Mateo, J.F. Sánchez-García, O. Arango, J. Egozcue and J. Benet

    Version of Record online : 12 FEB 2004, DOI: 10.1002/ajmg.a.30027

  17. Sex-specific chromosome instability in early human development

    American Journal of Medical Genetics Part A

    Volume 136A, Issue 4, 1 August 2005, Pages: 401–413, Natalia V. Kovaleva

    Version of Record online : 6 JUL 2005, DOI: 10.1002/ajmg.a.30815

  18. Cytogentic studies of a patient with mosaicism of isochromosome 13q and a dicentric (Y; 13) translocation showing differential centromeric activity

    Clinical Genetics

    Volume 24, Issue 3, September 1983, Pages: 194–199, Paul S. Ing and Shelley D. Smith

    Version of Record online : 28 JUN 2008, DOI: 10.1111/j.1399-0004.1983.tb02239.x

  19. Under-ascertainment of mosaic carriers of balanced homologous acrocentric translocations and isochromosomes

    American Journal of Medical Genetics Part A

    Volume 121A, Issue 2, 30 August 2003, Pages: 180–187, Natalia V. Kovaleva and Lisa G. Shaffer

    Version of Record online : 14 APR 2003, DOI: 10.1002/ajmg.a.20156

  20. Isochromosomes in neoplasia

    Genes, Chromosomes and Cancer

    Volume 10, Issue 4, August 1994, Pages: 221–230, Dr. Fredrik Mertens, Bertil Johansson and Felix Mitelman

    Version of Record online : 14 JUL 2006, DOI: 10.1002/gcc.2870100402