ABOUT US MEETINGS PUBLICATIONS RESEARCH LINKS

  • Sperber, G.H., Sperber, S.M., Guttmann G.
    Craniofacial Embryogenetics and Development
    People's Medical Publishing House-USA, (in Press, 2010)
     
  • Sperber, G.H., Sperber, S.M.
    Embryology of Orofacial Clefting" Chapter 1 in "Comprehensive Cleft Care
    Edited by J.E. Losee and R.E. Kirschner. New York: McGraw-Hill. 2009. Pps.1-20.
      
  • Salinas CF, Jorgenson RJ, Wright JT, DiGiovanna JJ, Fete MD
    2008 International Conference on Ectodermal Dysplasias Classification: conference report.
    Am J Med Genet A. 2009 Sep;149A(9):1958-69.
    PMID: 19681152
     
  • Fabiola Quintero-Rivera1,8, Caroline D. Robson2,8, Rosemary E. Reiss3,8, Deborah Levine4,8, Carol Benson5,8, John B. Mulliken6,8 and Virginia E. Kimonis7,8*
    Apert syndrome: what prenatal radiographic findings should prompt its consideration?
    Published online in Wiley InterScience (www.interscience.wiley.com) DOI: 10.1002/pd.1539
    Apert Prenatal Diagnosis 2006
     
  • Quintero-Rivera F, Robson CD, Reiss RE, Levine D, Benson CB, Mulliken JB, Kimonis VE. 2006.
    Intracranial anomalies detected by imaging studies in 30 patients with Apert syndrome.
    Am J Med Genet Part A 140A:1337–1338.
    Intracranial Anomalies Detected by Imaging Studies
     
  • Sperber G.H.
    The Genetics of Odontogenesis; Implications in Dental Anthropology and Palaeo-Odontology
    Dental Anthropology, 17:1-7, 2004.
     
  • Boyadjiev SA, Justice CM, Eyaid W, McKusick VA, Lachman RS, Chowdry AB, Jabak M, Zwaan J, Wilson AF, Jabs EW
    A novel dysmorphic syndrome with open calvarial sutures and sutural cataracts maps to chromosome 14q13-q21
    Hum Genet 2003 Apr 3
     
  • Paznekas WA, Boyadjiev SA, Shapiro RE, Daniels O, Wollnik B, Keegan CE, Innis JW, Dinulos MB, Christian C, Hannibal MC, Jabs EW.
    Connexin 43 (GJA1) mutations cause the pleiotropic phenotype of oculodentodigital dysplasia
    Am J Hum Genet 2003 Feb;72(2):408-18
      
  • Simeon A Boyadjiev, J Christopher Fromme, Jin Ben, Samuel S Chong, Christopher Nauta, David J Hur, George Zhang, Susan Hamamoto, Randy Schekman, Mariella Ravazzola, Lelio Orci, Wafaa Eyaid
    Cranio-lenticulo-sutural dysplasia is caused by a SEC23A mutation leading to abnormal endoplasmic-reticulum-to-Golgi trafficking
    Nature Genetics Advanced Online Publication: 
    Cranio-lenticulo-sutural dysplasia
     

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