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There are 21231 results for: content related to: A novel C2orf37 mutation causes the first Italian cases of Woodhouse Sakati syndrome

  1. C2orf37 mutational spectrum in Woodhouse–Sakati syndrome patients

    Clinical Genetics

    Volume 78, Issue 6, December 2010, Pages: 585–590, AM Alazami, SA Schneider, D Bonneau, L Pasquier, M Carecchio, M Kojovic, K Steindl, M De Kerdanet, MM Nezarati, KP Bhatia, B Degos, E Goh and FS Alkuraya

    Article first published online : 2 NOV 2010, DOI: 10.1111/j.1399-0004.2010.01441.x

  2. 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

  3. 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

  4. 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

  5. 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

  6. 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

  7. 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

  8. 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

  9. Human syndromes with congenital patellar anomalies and the underlying gene defects

    Clinical Genetics

    Volume 68, Issue 4, October 2005, Pages: 302–319, EMHF Bongers, A Van Kampen, H Van Bokhoven and NVAM Knoers

    Article first published online : 2 SEP 2005, DOI: 10.1111/j.1399-0004.2005.00508.x

  10. 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

  11. The molecular basis of variation in human color vision

    Clinical Genetics

    Volume 67, Issue 5, May 2005, Pages: 369–377, SS Deeb

    Article first published online : 22 FEB 2005, DOI: 10.1111/j.1399-0004.2004.00343.x

  12. Erratum

    Clinical Genetics

    Volume 64, Issue 2, August 2003, Pages: 176–177,

    Article first published online : 10 JUL 2003, DOI: 10.1034/j.1399-0004.2003.00141.x

  13. Intrachromosomal triplications: molecular cytogenetic and clinical studies

    Clinical Genetics

    Volume 58, Issue 2, August 2000, Pages: 134–141, Kavita S Reddy and James J Logan

    Article first published online : 24 DEC 2001, DOI: 10.1034/j.1399-0004.2000.580208.x

  14. 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

  15. 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

  16. Homozygosity for a novel DTDST mutation in a child with a ‘broad bone-platyspondylic’ variant of diastrophic dysplasia

    Clinical Genetics

    Volume 56, Issue 1, July 1999, Pages: 71–76, André Mégarbané, Fady A. Haddad, Soha Haddad-Zebouni, Mitri Achram, Georg Eich, Martine Le Merrer and Andrea Superti-Furga

    Article first published online : 24 DEC 2001, DOI: 10.1034/j.1399-0004.1999.560110.x

  17. Genetic epidemiology of alpha-1 antitrypsin deficiency in southern Europe: France, Italy, Portugal and Spain

    Clinical Genetics

    Volume 63, Issue 6, June 2003, Pages: 490–509, FJ De Serres, I Blanco and E Fernández-Bustillo

    Article first published online : 3 JUN 2003, DOI: 10.1034/j.1399-0004.2003.00078.x

  18. The Ehlers–Danlos syndrome, a disorder with many faces

    Clinical Genetics

    Volume 82, Issue 1, July 2012, Pages: 1–11, A De Paepe and F Malfait

    Article first published online : 15 MAR 2012, DOI: 10.1111/j.1399-0004.2012.01858.x

  19. Birth defects before epigenesis

    Clinical Genetics

    Volume 74, Issue 4, October 2008, Pages: 338–342, HA Tucker

    Article first published online : 28 JUN 2008, DOI: 10.1111/j.1399-0004.2008.01020.x

  20. Trisomy rescue by postzygotic unbalanced (X;14) translocation in a girl with dysmorphic features

    Clinical Genetics

    Volume 60, Issue 3, September 2001, Pages: 206–211, C Orellana, F Martínez, L Badía, JM Millán, MR Montero, J Andrés and F Prieto

    Article first published online : 12 JAN 2002, DOI: 10.1034/j.1399-0004.2001.600306.x