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There are 7864237 results for: content related to: Syndromes A, syndromes B, syndromes C

  1. Acute Myeloid Leukemia

    Cancer Cytogenetics, THIRD EDITION

    Bertil Johansson, Christine J. Harrison, Pages: 45–139, 2010

    Published Online : 4 OCT 2010, DOI: 10.1002/9781118010136.ch5

  2. Diabetic neuropathy: new strategies for treatment

    Diabetes, Obesity and Metabolism

    Volume 10, Issue 2, February 2008, Pages: 99–108, Tamás Várkonyi and Peter Kempler

    Version of Record online : 26 JUN 2007, DOI: 10.1111/j.1463-1326.2007.00741.x

  3. The MEF2C gene-microdeletion 5q14.3 dilemma and three axioms for molecular syndromology

    American Journal of Medical Genetics Part A

    Volume 161, Issue 4, April 2013, Pages: 916–917, Golder N. Wilson

    Version of Record online : 12 MAR 2013, DOI: 10.1002/ajmg.a.35785

  4. Human disorganization complex, as a polytopic blastogenesis defect: A new case

    American Journal of Medical Genetics Part A

    Volume 125A, Issue 2, 1 March 2004, Pages: 181–185, Wilmer Noé Delgado Luengo, María Luisa Hernández Rodríguez, Ivonne Valbuena Pirela, Sandra González Ferrer, Pedro Estrada Corona, Inara Chacón Fonseca, Juana Delgado Luengo, Alisandra Morales-Machín, Lisbeth Borjas Fuentes, María Caridad Martínez Basalo and José Chacín

    Version of Record online : 31 JUL 2003, DOI: 10.1002/ajmg.a.20307

  5. Fusion of the AHRR and NCOA2 genes through a recurrent translocation t(5;8)(p15;q13) in soft tissue angiofibroma results in upregulation of aryl hydrocarbon receptor target genes

    Genes, Chromosomes and Cancer

    Volume 51, Issue 5, May 2012, Pages: 510–520, Yuesheng Jin, Emely Möller, Karolin H. Nord, Nils Mandahl, Fredrik Vult Von Steyern, Henryk A. Domanski, Adrian Mariño-Enríquez, Linda Magnusson, Jenny Nilsson, Raf Sciot, Christopher D. M. Fletcher, Maria Debiec-Rychter and Fredrik Mertens

    Version of Record online : 15 FEB 2012, DOI: 10.1002/gcc.21939

  6. You have free access to this content
    Update in clinical allergy and immunology

    Allergy

    Volume 67, Issue 12, December 2012, Pages: 1491–1500, S. von Gunten, B. J. Marsland, C. von Garnier and D. Simon

    Version of Record online : 30 OCT 2012, DOI: 10.1111/all.12067

  7. Sirenomelia and caudal malformations in two families

    American Journal of Medical Genetics Part A

    Volume 158A, Issue 7, July 2012, Pages: 1801–1807, Marion Gerard, Valérie Layet, Teresa Costa, Yves Roumazeilles, Pierre Chenal, Daniel Cailliez and Bénédicte Gerard

    Version of Record online : 20 APR 2012, DOI: 10.1002/ajmg.a.35408

  8. Differential expression of moesin in breast cancers and its implication in epithelial–mesenchymal transition

    Histopathology

    Volume 61, Issue 1, July 2012, Pages: 78–87, Chung-Chieh Wang, Jau-Yu Liau, Yen-Shen Lu, Jun-Wei Chen, Yu-Tung Yao and Huang-Chun Lien

    Version of Record online : 22 MAR 2012, DOI: 10.1111/j.1365-2559.2012.04204.x

  9. Invited editorial comment: Further reflections on gastroschisis

    American Journal of Medical Genetics Part C: Seminars in Medical Genetics

    Volume 148C, Issue 3, 15 August 2008, Pages: 192–198, John M. Opitz and Theodore J. Pysher

    Version of Record online : 24 JUL 2008, DOI: 10.1002/ajmg.c.30177

  10. You have free access to this content
    The role of compliance in optimizing the ocular surface after two-step LASIK

    Acta Ophthalmologica

    Volume 90, Issue s249, September 2012, Page: 0, M SERGEEVA, M KOVALEVSKAYA and I CHERNIKOVA

    Version of Record online : 6 AUG 2012, DOI: 10.1111/j.1755-3768.2012.T047.x

  11. Osteocraniostenosis–hypomineralized skull with gracile long bones and splenic hypoplasia. Four new cases with distinctive chondro-osseous morphology

    American Journal of Medical Genetics Part A

    Volume 140A, Issue 14, 15 July 2006, Pages: 1553–1563, Alison M. Elliott, William R. Wilcox, Gerald S. Spear, Fiona M. Field, Thora S. Steffensen, Barbara D. Friedman, David L. Rimoin and Ralph S. Lachman

    Version of Record online : 12 JUN 2006, DOI: 10.1002/ajmg.a.31326

  12. First 25 years of the Hungarian congenital abnormality registry

    Teratology

    Volume 55, Issue 5, May 1997, Pages: 299–305, A. E. Czeizel

    Version of Record online : 7 DEC 1998, DOI: 10.1002/(SICI)1096-9926(199705)55:5<299::AID-TERA1>3.0.CO;2-V

  13. Boveri at 100: Boveri, chromosomes and cancer

    The Journal of Pathology

    Volume 234, Issue 2, October 2014, Pages: 138–141, Sverre Heim

    Version of Record online : 10 SEP 2014, DOI: 10.1002/path.4406

  14. Malformations of the craniofacial region: Evolutionary, embryonic, genetic, and clinical perspectives

    American Journal of Medical Genetics

    Volume 115, Issue 4, 30 December 2002, Pages: 245–268, M. Michael Cohen Jr.

    Version of Record online : 23 DEC 2002, DOI: 10.1002/ajmg.10982

  15. Anal atresia, vertebral, genital, and urinary tract anomalies: A primary polytopic developmental field defect identified through an epidemiological analysis of associations

    American Journal of Medical Genetics

    Volume 95, Issue 2, 13 November 2000, Pages: 169–173, M.L. Martínez-Frías, E. Bermejo and E. Rodríguez-Pinilla

    Version of Record online : 8 NOV 2000, DOI: 10.1002/1096-8628(20001113)95:2<169::AID-AJMG15>3.0.CO;2-Z

  16. Gene fusions in soft tissue tumors: Recurrent and overlapping pathogenetic themes

    Genes, Chromosomes and Cancer

    Volume 55, Issue 4, April 2016, Pages: 291–310, Fredrik Mertens, Cristina R. Antonescu and Felix Mitelman

    Version of Record online : 18 DEC 2015, DOI: 10.1002/gcc.22335

  17. ADAM “sequence” part II: Hypothesis and speculation

    American Journal of Medical Genetics Part A

    Volume 167, Issue 3, March 2015, Pages: 478–503, John M. Opitz, Dennis R. Johnson and Enid F. Gilbert-Barness

    Version of Record online : 21 JAN 2015, DOI: 10.1002/ajmg.a.36937

  18. You have free access to this content
    Systemic sclerosis – dermatological aspects. Part 1: Pathogenesis, epidemiology, clinical findings

    JDDG: Journal der Deutschen Dermatologischen Gesellschaft

    Volume 10, Issue 10, October 2012, Pages: 705–716, Michael Sticherling

    Version of Record online : 22 AUG 2012, DOI: 10.1111/j.1610-0387.2012.07999.x

  19. Disease-associated patterns of disomic chromosomes in hyperhaploid neoplasms

    Genes, Chromosomes and Cancer

    Volume 51, Issue 6, June 2012, Pages: 536–544, Nils Mandahl, Bertil Johansson, Fredrik Mertens and Felix Mitelman

    Version of Record online : 15 FEB 2012, DOI: 10.1002/gcc.21947

  20. A novel GTF2I/NCOA2 fusion gene emphasizes the role of NCOA2 in soft tissue angiofibroma development

    Genes, Chromosomes and Cancer

    Volume 52, Issue 3, March 2013, Pages: 330–331, Elsa Arbajian, Linda Magnusson, Fredrik Mertens, Henryk A. Domanski, Fredrik Vult von Steyern and Karolin H. Nord

    Version of Record online : 10 DEC 2012, DOI: 10.1002/gcc.22033