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There are 15789 results for: content related to: Mild nasal malformations and parietal foramina caused by homozygous ALX4 mutations

  1. Skull defects, alopecia, hypertelorism, and notched alae nasi caused by homozygous ALX4 gene mutation

    American Journal of Medical Genetics Part A

    Volume 164, Issue 5, May 2014, Pages: 1322–1327, Ariana Kariminejad, Bita Bozorgmehr, Houman Alizadeh, Siavash Ghaderi-Sohi, Güven Toksoy, Zehra Oya Uyguner and Hülya Kayserili

    Version of Record online : 25 MAR 2014, DOI: 10.1002/ajmg.a.36008

  2. You have free access to this content
    Pattern formation in the vascular system of monocot and dicot plant species

    New Phytologist

    Volume 164, Issue 2, November 2004, Pages: 209–242, Enrico Scarpella and Annemarie H. Meijer

    Version of Record online : 20 SEP 2004, DOI: 10.1111/j.1469-8137.2004.01191.x

  3. ECEL1 mutation causes fetal arthrogryposis multiplex congenita

    American Journal of Medical Genetics Part A

    Volume 167, Issue 4, April 2015, Pages: 731–743, N. Dohrn, V.Q. Le, A. Petersen, P. Skovbo, I.S. Pedersen, A. Ernst, H. Krarup and M.B. Petersen

    Version of Record online : 23 FEB 2015, DOI: 10.1002/ajmg.a.37018

  4. Systemic Treatment of Pediatric Atopic Dermatitis with Azathioprine and Mycophenolate Mofetil

    Pediatric Dermatology

    Volume 28, Issue 6, November/December 2011, Pages: 689–694, Weston T. Waxweiler, Robert Agans and Dean S. Morrell

    Version of Record online : 4 OCT 2011, DOI: 10.1111/j.1525-1470.2011.01488.x

  5. Epilepsy due to mutations in the mitochondrial polymerase gamma (POLG) gene: A clinical and molecular genetic review

    Epilepsia

    Volume 57, Issue 10, October 2016, Pages: 1531–1545, Maria-Eleni Anagnostou, Yi Shiau Ng, Robert W. Taylor and Robert McFarland

    Version of Record online : 24 AUG 2016, DOI: 10.1111/epi.13508

  6. Analysis of ASPM in an ethnically diverse cohort of 400 patient samples: perspectives of the molecular diagnostic laboratory

    Clinical Genetics

    Volume 85, Issue 4, April 2014, Pages: 353–358, CA Tan, D. del Gaudio, M.A. Dempsey, K. Arndt, S. Botes, A. Reeder and S. Das

    Version of Record online : 13 MAY 2013, DOI: 10.1111/cge.12172

  7. The ABCB1-1Δ mutation is not responsible for subchronic neurotoxicity seen in dogs of non-collie breeds following macrocyclic lactone treatment for generalized demodicosis

    Veterinary Dermatology

    Volume 20, Issue 1, February 2009, Pages: 60–66, Stéphane Bissonnette, Manon Paradis, Isabelle Daneau and David W. Silversides

    Version of Record online : 18 DEC 2008, DOI: 10.1111/j.1365-3164.2008.00731.x

  8. Chromosomal microarray in a highly consanguineous population: diagnostic yield, utility of regions of homozygosity, and novel mutations

    Clinical Genetics

    M.A. Alabdullatif, M.A. Al Dhaibani, M.Y. Khassawneh and A.W. El-Hattab

    Version of Record online : 11 OCT 2016, DOI: 10.1111/cge.12872

  9. Novel mutation in the ALS2 gene in juvenile amyotrophic lateral sclerosis

    Annals of Neurology

    Volume 58, Issue 5, November 2005, Pages: 800–803, Julia A. Kress, Peter Kühnlein, Pia Winter, Albert C. Ludolph, Jan Kassubek, Ulrich Müller and Anne-Dorte Sperfeld

    Version of Record online : 20 OCT 2005, DOI: 10.1002/ana.20665

  10. Determination of a New Mutation in MT-ND1 Gene of a Patient With Dextrocardia, Ventriculoarterial Discordance, and Tricuspid Atresia

    Artificial Organs

    Volume 39, Issue 1, January 2015, Pages: 83–84, Ali Can Hatemi, Hakan Ceyran and Duran Üstek

    Version of Record online : 27 JAN 2015, DOI: 10.1111/aor.12442

  11. Molecular analysis and clinical aspects of four patients with Chédiak-Higashi syndrome (CHS)

    Clinical Genetics

    Volume 76, Issue 4, October 2009, Pages: 409–412, E Scherber, K Beutel, R Ganschow, A Schulz, G Janka and U zur Stadt

    Version of Record online : 24 JUL 2009, DOI: 10.1111/j.1399-0004.2009.01205.x

  12. Abstracts from the Tenth International Conference on Pediatric Mechanical Circulatory Support Systems and Pediatric Cardiopulmonary Bypass

    Artificial Organs

    Volume 38, Issue 5, May 2014, Pages: A1–A17,

    Version of Record online : 28 APR 2014, DOI: 10.1111/aor.12324

  13. Potocki–shaffer deletion encompassing ALX4 in a patient with frontonasal dysplasia phenotype

    American Journal of Medical Genetics Part A

    Volume 164, Issue 2, February 2014, Pages: 346–352, Alessandra Ferrarini, Muriel Gaillard, Frederic Guerry, Gianpaolo Ramelli, Fodstad Heidi, Caroline Verley Keddache, Ilse Wieland, Jacques S. Beckmann, Sébastien Jaquemont and Danielle Martinet

    Version of Record online : 13 DEC 2013, DOI: 10.1002/ajmg.a.36140

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    Molecular basis of Bernard–Soulier syndrome in 27 patients from India

    Journal of Thrombosis and Haemostasis

    Volume 9, Issue 8, August 2011, Pages: 1590–1598, E. SUMITHA, G. R. JAYANDHARAN, S. DAVID, R. R. JACOB, G. SANKARI DEVI, B. BARGAVI, S. SHENBAGAPRIYA, S. C. NAIR, A. ABRAHAM, B. GEORGE, A. VISWABANDYA, V. MATHEWS, M. CHANDY and A. SRIVASTAVA

    Version of Record online : 11 AUG 2011, DOI: 10.1111/j.1538-7836.2011.04417.x

  15. Further delineation of the clinical spectrum in RNU4ATAC related microcephalic osteodysplastic primordial dwarfism type I

    American Journal of Medical Genetics Part A

    Volume 161, Issue 8, August 2013, Pages: 1875–1881, Ghada M.H. Abdel-Salam, Mohamed S. Abdel-Hamid, Nihal A. Hassan, Mahmoud Y. Issa, Laila Effat, Samira Ismail, Mona S. Aglan and Maha S. Zaki

    Version of Record online : 21 JUN 2013, DOI: 10.1002/ajmg.a.36009

  16. Molecular characterization of commonly used cell lines for bone tumor research: A trans-European EuroBoNet effort

    Genes, Chromosomes and Cancer

    Volume 49, Issue 1, January 2010, Pages: 40–51, Laura Ottaviano, Karl-Ludwig Schaefer, Melanie Gajewski, Wolfgang Huckenbeck, Stefan Baldus, Uwe Rogel, Carlos Mackintosh, Enrique de Alava, Ola Myklebost, Stine H. Kresse, Leonardo A. Meza-Zepeda, Massimo Serra, Anne-Marie Cleton-Jansen, Pancras C. W. Hogendoorn, Horst Buerger, Thomas Aigner, Helmut E. Gabbert and Christopher Poremba

    Version of Record online : 29 SEP 2009, DOI: 10.1002/gcc.20717

  17. Molecular basis of quantitative fibrinogen disorders in 27 patients from India

    Haemophilia

    Volume 19, Issue 4, July 2013, Pages: 611–618, E. Sumitha, G. R. Jayandharan, N. Arora, A. Abraham, S. David, G. S. Devi, P. Shenbagapriya, S. C. Nair, B. George, V. Mathews, M. Chandy, A. Viswabandya and A. Srivastava

    Version of Record online : 8 APR 2013, DOI: 10.1111/hae.12143

  18. Comparative study of the structure of chromosome 1R derived from Secale montanum and Secale cereale

    Plant Breeding

    Volume 134, Issue 6, December 2015, Pages: 675–683, Jianjian Li, Yadav Prasad Gyawali, Ruonan Zhou, Nils Stein, Shuhei Nasuda and Takashi R. Endo

    Version of Record online : 23 OCT 2015, DOI: 10.1111/pbr.12314

  19. Novel homozygous ALX4 mutation causing frontonasal dysplasia-2 in a patient with meningoencephalocele

    Clinical Genetics

    Volume 88, Issue 6, December 2015, Pages: 593–596, V.A. Meloni, M. Moysés-Oliveira, M.C.C. Melo, T.P. Caneloi, A.G. Dantas, M.F.F. Soares, R. Fock, P.D. Rodrigues de Nicola, M.R. Dias-da-Silva and M.I. Melaragno

    Version of Record online : 11 MAY 2015, DOI: 10.1111/cge.12595

  20. Apolipoprotein E and Paraoxonase 1 polymorphisms are associated with lower serum thyroid hormones in postmenopausal women

    Clinical Endocrinology

    Volume 71, Issue 2, August 2009, Pages: 284–290, Irene Lambrinoudaki, George Kaparos, Demetrios Rizos, Fotini Galapi, Andreas Alexandrou, Theodoros N. Sergentanis, Maria Creatsa, George Christodoulakos, E. Kouskouni and D. Botsis

    Version of Record online : 9 NOV 2008, DOI: 10.1111/j.1365-2265.2008.03476.x