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There are 10286 results for: content related to: Homozygous FGF3 mutations result in congenital deafness with inner ear agenesis, microtia, and microdontia

  1. You have free access to this content
    LAMM syndrome with middle ear dysplasia associated with compound heterozygosity for FGF3 mutations

    American Journal of Medical Genetics Part A

    Volume 155, Issue 5, May 2011, Pages: 1096–1101, Alberto Sensi, Stefano Ceruti, Patrizia Trevisi, Francesca Gualandi, Micol Busi, Ilaria Donati, Marcella Neri, Alessandra Ferlini and Alessandro Martini

    Version of Record online : 7 APR 2011, DOI: 10.1002/ajmg.a.33962

  2. A FGF3 mutation associated with differential inner ear malformation, microtia, and microdontia

    The Laryngoscope

    Volume 120, Issue 2, February 2010, Pages: 359–364, Reinhard Ramsebner, Martin Ludwig, Thomas Parzefall, Trevor Lucas, Wolf-Dieter Baumgartner, Olaf Bodamer, Filiz Basak Cengiz, Christian Schoefer, Mustafa Tekin and Klemens Frei

    Version of Record online : 30 NOV 2009, DOI: 10.1002/lary.20689

  3. You have full text access to this OnlineOpen article
    The Fibroblast Growth Factor signaling pathway

    Wiley Interdisciplinary Reviews: Developmental Biology

    Volume 4, Issue 3, May/June 2015, Pages: 215–266, David M. Ornitz and Nobuyuki Itoh

    Version of Record online : 13 MAR 2015, DOI: 10.1002/wdev.176

  4. You have full text access to this OnlineOpen article
    Scientific Opinion on an application by Bayer CropScience and Monsanto (EFSA-GMO-NL-2009-75) for placing on the market of genetically modified glufosinate-ammonium- and glyphosate-tolerant oilseed rape MS8 × RF3 × GT73 and subcombinations, which have not been authorised previously (i.e. MS8 × GT73 and RF3 × GT73) independently of their origin, for food and feed uses, import and processing, with the exception of isolated seed protein for food, under Regulation (EC) No 1829/2003

    EFSA Journal

    Volume 14, Issue 5, May 2016, EFSA Panel on Genetically Modified Organisms (GMO)

    Version of Record online : 20 MAY 2016, DOI: 10.2903/j.efsa.2016.4466

  5. Molecular pathology of the fibroblast growth factor family

    Human Mutation

    Volume 30, Issue 9, September 2009, Pages: 1245–1255, Pavel Krejci, Jirina Prochazkova, Vitezslav Bryja, Alois Kozubik and William R. Wilcox

    Version of Record online : 16 JUN 2009, DOI: 10.1002/humu.21067

  6. Repair of non-understanding in English in international communication

    World Englishes

    Volume 27, Issue 3-4, August/November 2008, Pages: 378–406, MATTHEW WATTERSON

    Version of Record online : 30 OCT 2008, DOI: 10.1111/j.1467-971X.2008.00574.x

  7. Preferential Associated Anomalies in 818 Cases of Microtia in South America

    American Journal of Medical Genetics Part A

    Volume 161, Issue 5, May 2013, Pages: 1051–1057, Daniela V. Luquetti, Timothy C. Cox, Jorge Lopez-Camelo, Maria da Graça Dutra, Michael L. Cunningham and Eduardo E. Castilla

    Version of Record online : 29 MAR 2013, DOI: 10.1002/ajmg.a.35888

  8. Diseases of the tooth: the genetic and molecular basis of inherited anomalies affecting the dentition

    Wiley Interdisciplinary Reviews: Developmental Biology

    Volume 2, Issue 2, March/April 2013, Pages: 183–212, Martyn T. Cobourne and Paul T. Sharpe

    Version of Record online : 25 MAY 2012, DOI: 10.1002/wdev.66

  9. Epidemiologic characteristics and time trend in the prevalence of anotia and microtia in China

    Birth Defects Research Part A: Clinical and Molecular Teratology

    Volume 106, Issue 2, February 2016, Pages: 88–94, Kui Deng, Li Dai, Ling Yi, Changfei Deng, Xiaohong Li and Jun Zhu

    Version of Record online : 17 DEC 2015, DOI: 10.1002/bdra.23462

  10. Sociodemographic and hispanic acculturation factors and isolated anotia/microtia

    Birth Defects Research Part A: Clinical and Molecular Teratology

    Volume 100, Issue 11, November 2014, Pages: 852–862, Adrienne T. Hoyt, Mark A. Canfield, Gary M. Shaw, Dorothy K. Waller, Kara N.D. Polen, Tunu Ramadhani, Marlene T. Anderka, Angela E. Scheuerle and the National Birth Defects Prevention Study

    Version of Record online : 30 JUL 2014, DOI: 10.1002/bdra.23282

  11. You have full text access to this OnlineOpen article
    HOXA2 Haploinsufficiency in Dominant Bilateral Microtia and Hearing Loss

    Human Mutation

    Volume 34, Issue 10, October 2013, Pages: 1347–1351, Kerry K. Brown, Lucas M. Viana, Cecilia C. Helwig, Maria A. Artunduaga, Lourdes Quintanilla-Dieck, Patricia Jarrin, Gabriel Osorno, Barbara McDonough, Steven R. DePalma, Roland D. Eavey, Jonathan G. Seidman and Christine E. Seidman

    Version of Record online : 11 JUL 2013, DOI: 10.1002/humu.22367

  12. Epidemiologic features and clinical subgroups of anotia/microtia in Texas

    Birth Defects Research Part A: Clinical and Molecular Teratology

    Volume 85, Issue 11, November 2009, Pages: 905–913, Mark A. Canfield, Peter H. Langlois, Ly M. Nguyen and Angela E. Scheuerle

    Version of Record online : 16 SEP 2009, DOI: 10.1002/bdra.20626

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    Signaling regulating inner ear development: Cell fate determination, patterning, morphogenesis, and defects

    Congenital Anomalies

    Volume 55, Issue 1, February 2015, Pages: 17–25, Yuji Nakajima

    Version of Record online : 15 JAN 2015, DOI: 10.1111/cga.12072

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    Yeast Arf3p Modulates Plasma Membrane PtdIns(4,5)P2 Levels to Facilitate Endocytosis

    Traffic

    Volume 9, Issue 4, April 2008, Pages: 559–573, Iwona I. Smaczynska-de Rooij, Rosaria Costa and Kathryn R Ayscough

    Version of Record online : 15 JAN 2008, DOI: 10.1111/j.1600-0854.2008.00708.x

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    Microtia: Epidemiology and genetics

    American Journal of Medical Genetics Part A

    Volume 158A, Issue 1, January 2012, Pages: 124–139, Daniela V. Luquetti, Carrie L. Heike, Anne V. Hing, Michael L. Cunningham and Timothy C. Cox

    Version of Record online : 21 NOV 2011, DOI: 10.1002/ajmg.a.34352

  16. Descriptive epidemiology of anotia and microtia, Hawaii, 1986–2002

    Congenital Anomalies

    Volume 45, Issue 4, December 2005, Pages: 119–124, Mathias B. Forrester and Ruth D. Merz

    Version of Record online : 30 NOV 2005, DOI: 10.1111/j.1741-4520.2005.00080.x

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    Rho1-GEFs Rgf1 and Rgf2 are involved in formation of cell wall and septum, while Rgf3 is involved in cytokinesis in fission yeast

    Genes to Cells

    Volume 10, Issue 12, December 2005, Pages: 1189–1202, Tadashi Mutoh, Kentaro Nakano and Issei Mabuchi

    Version of Record online : 10 NOV 2005, DOI: 10.1111/j.1365-2443.2005.00908.x

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    In this issue

    American Journal of Medical Genetics Part A

    Volume 155, Issue 5, May 2011, Page: x,

    Version of Record online : 19 APR 2011, DOI: 10.1002/ajmg.a.34062

  19. Risk factors and demographics for microtia in South America: A case–control analysis

    Birth Defects Research Part A: Clinical and Molecular Teratology

    Volume 97, Issue 11, November 2013, Pages: 736–743, Daniela V. Luquetti, Babette S. Saltzman, Jorge Lopez-Camelo, Maria da Graça Dutra and Eduardo E. Castilla

    Version of Record online : 21 NOV 2013, DOI: 10.1002/bdra.23193

  20. Difference in Facial Canal Anatomy in Terms of Severity of Microtia and Deformity of Middle Ear in Patients With Microtia

    The Laryngoscope

    Volume 113, Issue 4, April 2003, Pages: 635–639, Hideki Takegoshi and Kimitaka Kaga

    Version of Record online : 2 JAN 2009, DOI: 10.1097/00005537-200304000-00009