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There are 69450 results for: content related to: Hippocampus development and function: role of epigenetic factors and implications for cognitive disease

  1. Chromodomain proteins in development: lessons from CHARGE syndrome

    Clinical Genetics

    Volume 78, Issue 1, July 2010, Pages: 11–20, WS Layman, EA Hurd and DM Martin

    Article first published online : 8 APR 2010, DOI: 10.1111/j.1399-0004.2010.01446.x

  2. The molecular basis for developmental disorders of the pituitary gland in man

    Clinical Genetics

    Volume 57, Issue 5, May 2000, Pages: 337–346, Mt Dattani and Ic Robinson

    Article first published online : 24 DEC 2001, DOI: 10.1034/j.1399-0004.2000.570503.x

  3. The hemoglobinopathies and malaria

    Clinical Genetics

    Volume 68, Issue 4, October 2005, Pages: 332–336, J Richer and AE Chudley

    Article first published online : 19 AUG 2005, DOI: 10.1111/j.1399-0004.2005.00503.x

  4. Understanding the population structure of North American patients with cystic fibrosis

    Clinical Genetics

    Volume 79, Issue 2, February 2011, Pages: 136–146, W Li, L Sun, M Corey, F Zou, S Lee, AL Cojocaru, C Taylor, SM Blackman, A Stephenson, AJ Sandford, R Dorfman, ML Drumm, GR Cutting, MR Knowles, P Durie, FA Wright and LJ Strug

    Article first published online : 2 JUL 2010, DOI: 10.1111/j.1399-0004.2010.01502.x

  5. History of genetics through philately – deafness

    Clinical Genetics

    Volume 60, Issue 6, December 2001, Pages: 417–420, SM Nikkel and AE Chudley

    Article first published online : 11 JAN 2002, DOI: 10.1034/j.1399-0004.2001.600603.x

  6. Landmarks in genetics through philately: the tools used by dysmorphologists

    Clinical Genetics

    Volume 63, Issue 2, February 2003, Pages: 105–108, AE Chudley

    Article first published online : 10 MAR 2003, DOI: 10.1034/j.1399-0004.2003.00030.x

  7. Retinal detachment and cataract, facial dysmorphism, generalized osteoporosis, immobile spine and platyspondyly in a consanguinous kindred – a possible new syndrome

    Clinical Genetics

    Volume 59, Issue 2, February 2001, Pages: 99–105, H Schmidt, G Rudolph, M Hergersberg, K Schneider, S Moradi and T Meitinger*

    Article first published online : 20 DEC 2001, DOI: 10.1034/j.1399-0004.2001.590206.x

  8. Familial CHARGE syndrome because of CHD7 mutation: clinical intra- and interfamilial variability

    Clinical Genetics

    Volume 72, Issue 2, August 2007, Pages: 112–121, A Delahaye, Y Sznajer, S Lyonnet, M Elmaleh-Bergès, I Delpierre, S Audollent, S Wiener-Vacher, A-L Mansbach, J Amiel, C Baumann, D Bremond-Gignac, T Attié-Bitach, A Verloes and D Sanlaville

    Article first published online : 20 JUL 2007, DOI: 10.1111/j.1399-0004.2007.00821.x

  9. Interpupillary distance in a normal black population

    Clinical Genetics

    Volume 55, Issue 3, March 1999, Pages: 182–191, EK Pivnick, ML Rivas, EA Tolley, SD Smith and GJ Presbury

    Article first published online : 24 DEC 2001, DOI: 10.1034/j.1399-0004.1999.550306.x

  10. Partial DiGeorge syndrome in two patients with a 10p rearrangement

    Clinical Genetics

    Volume 55, Issue 4, April 1999, Pages: 269–276, Hilde Van Esch, Peter Groenen, Sarah Daw, Ann Poffyn, Maureen Holvoet, Peter Scambler, Jean-Pierre Fryns, Wim Van de Ven and Koen Devriendt

    Article first published online : 24 DEC 2001, DOI: 10.1034/j.1399-0004.1999.550410.x

  11. A new classification system for primary lymphatic dysplasias based on phenotype

    Clinical Genetics

    Volume 77, Issue 5, May 2010, Pages: 438–452, F Connell, G Brice, S Jeffery, V Keeley, P Mortimer and S Mansour

    Article first published online : 11 FEB 2010, DOI: 10.1111/j.1399-0004.2010.01394.x

  12. Multi-organellar disorders of pigmentation: tied up in traffic

    Clinical Genetics

    Volume 55, Issue 5, May 1999, Pages: 309–317, Richard A Spritz

    Article first published online : 24 DEC 2001, DOI: 10.1034/j.1399-0004.1999.550503.x

  13. Mechanisms regulating the development of the corpus callosum and its agenesis in mouse and human

    Clinical Genetics

    Volume 66, Issue 4, October 2004, Pages: 276–289, LJ Richards, C Plachez and T Ren

    Article first published online : 8 SEP 2004, DOI: 10.1111/j.1399-0004.2004.00354.x

  14. Molecular analysis of 30 Niemann–Pick type C patients from Spain

    Clinical Genetics

    Volume 80, Issue 1, July 2011, Pages: 39–49, J Macías-Vidal, L Rodríguez-Pascau, G Sánchez-Ollé, M Lluch, L Vilageliu, D Grinberg, MJ Coll and the Spanish NPC Working Group

    Article first published online : 6 JUL 2010, DOI: 10.1111/j.1399-0004.2010.01504.x

  15. 40 years of the annual ‘Bar Harbor Course’ (1960–1999): a pictorial history

    Clinical Genetics

    Volume 55, Issue 6, June 1999, Pages: 398–415, Victor A McKusick, Juergen Naggert, Patsy Nishina and David Valle

    Article first published online : 24 DEC 2001, DOI: 10.1034/j.1399-0004.1999.550603.x

  16. Transcervical cells and the prenatal diagnosis of haemoglobin (Hb) mutations

    Clinical Genetics

    Volume 56, Issue 5, November 1999, Pages: 358–362, V Cirigliano, J Sherlock, M Petrou, Rht Ward, C Rodeck and M Adinolfi

    Article first published online : 24 DEC 2001, DOI: 10.1034/j.1399-0004.1999.560503.x

  17. Proven germline mosaicism in a father of two children with CHARGE syndrome

    Clinical Genetics

    Volume 75, Issue 5, May 2009, Pages: 473–479, S Pauli, L Pieper, J Häberle, P Grzmil, P Burfeind, M Steckel, U Lenz and HW Michelmann

    Article first published online : 17 MAR 2009, DOI: 10.1111/j.1399-0004.2009.01151.x

  18. Chimera and other fertilization errors

    Clinical Genetics

    Volume 70, Issue 5, November 2006, Pages: 363–373, V Malan, M Vekemans and C Turleau

    Article first published online : 14 SEP 2006, DOI: 10.1111/j.1399-0004.2006.00689.x

  19. Identification of four novel mutations in five unrelated Korean families with Fabry disease

    Clinical Genetics

    Volume 58, Issue 3, September 2000, Pages: 228–233, J-K Lee, G-H Kim, J-S Kim, K-K Kim, M-C Lee and H-W Yoo

    Article first published online : 24 DEC 2001, DOI: 10.1034/j.1399-0004.2000.580311.x

  20. New insights in congenital bowing of the femora

    Clinical Genetics

    Volume 66, Issue 3, September 2004, Pages: 169–176, V Cormier-Daire, D Geneviève, A Munnich and M Le Merrer

    Article first published online : 20 AUG 2004, DOI: 10.1111/j.0009-9163.2004.00307.x