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  • 1 Semmelweis Egyetem, Általános Orvostudományi Kar I. Szülészeti és Nőgyógyászati Klinika Budapest Baross u. 27. 1088
  • | 2 Fővárosi Egyesített Szent István és Szent László Kórház Budapest
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  • Abuelo, D.: Microcephaly syndromes. Semin. Pediatr. Neurol., 2007, 14, 118–127.

    Abuelo D. , 'Microcephaly syndromes ' (2007 ) 14 Semin. Pediatr. Neurol. : 118 -127.

  • Bronsteen, R. A., Comstock, C. H.: Central nervous system anomalies. Clin. Perinatol., 2000, 27, 791–812.

    Comstock C. H. , 'Central nervous system anomalies ' (2000 ) 27 Clin. Perinatol. : 791 -812.

  • Dahlgren, L., Wilson, R. D.: Prenatally diagnosed microcephaly: a review of etiologies. Fetal Diagn. Ther., 2001, 16, 323–326.

    Wilson R. D. , 'Prenatally diagnosed microcephaly: a review of etiologies ' (2001 ) 16 Fetal Diagn. Ther. : 323 -326.

    • Search Google Scholar
  • Darvish, H., Esmaeeli-Nieh, S., Monajemi, G. B. és mtsai: A clinical and molecular genetic study of 112 Iranian families with primary microcephaly. J. Med. Genet., 2010, 47, 823–828.

    Monajemi G. B. , 'A clinical and molecular genetic study of 112 Iranian families with primary microcephaly ' (2010 ) 47 J. Med. Genet. : 823 -828.

    • Search Google Scholar
  • Desir, J., Abramowicz, M., Tunca, Y.: Novel mutations in prenatal diagnosis of primary microcephaly. Prenat. Diagn., 2006, 26, 989.

    Tunca Y. , 'Novel mutations in prenatal diagnosis of primary microcephaly ' (2006 ) 26 Prenat. Diagn. : 989 -.

    • Search Google Scholar
  • Mochida, G. H.: Molecular genetics of lissencephaly and microcephaly. Brain Nerve, 2008, 60, 437–444.

    Mochida G. H. , 'Molecular genetics of lissencephaly and microcephaly ' (2008 ) 60 Brain Nerve : 437 -444.

    • Search Google Scholar
  • Papp, Z., Tóth-Pál, E., Papp, Cs. és mtsai: Impact of prenatal mid-trimester screening on the prevalence of fetal structural anomalies: a prospective epidemiological study. Ultrasound Obstet. Gynecol., 1995, 6, 320–326.

    Papp Cs. , 'Impact of prenatal mid-trimester screening on the prevalence of fetal structural anomalies: a prospective epidemiological study ' (1995 ) 6 Ultrasound Obstet. Gynecol. : 320 -326.

    • Search Google Scholar
  • Tang, C. J., Lin, S. Y., Hsu, W. B. és mtsai: The human microcephaly protein STIL interacts with CPAP and is required for procentriole formation. EMBO J., 2011 Oct 21., DOI:10.1038/emboj.2011.378

    Hsu W. B. , 'The human microcephaly protein STIL interacts with CPAP and is required for procentriole formation ' (2011 ) EMBO J. : -.

    • Search Google Scholar
  • Tolmie, J. L.: Prenatal diagnosis of microcephaly. Prenat. Diagn., 1991, 11, 347.

    Tolmie J. L. , 'Prenatal diagnosis of microcephaly ' (1991 ) 11 Prenat. Diagn. : 347 -.

  • Adama van Scheltema, P. N., Nagel, H. T. C, Brouwer, O. F. és mtsa: Outcome of children with prenatally diagnosed central nervous system malformations. Ultrasound Obstet. Gynecol., 2003, 21, 41–47.

    Brouwer O. F. , 'Outcome of children with prenatally diagnosed central nervous system malformations ' (2003 ) 21 Ultrasound Obstet. Gynecol. : 41 -47.

    • Search Google Scholar
  • Vannucci, R. C., Barron, T. F., Vannucci, S. J.: Craniometric measures of microcephaly using MRI. Early Hum. Dev., 2011 Aug 3. [Epub ahead of print] PubMed PMID: 21820253

  • Woods, C. G., Bond, J., Enard, W.: Autosomal recessive primary microcephaly (MCPH): a review of clinical, molecular, and evolutionary findings. Am. J. Hum. Genet., 2005, 76, 717–728.

    Enard W. , 'Autosomal recessive primary microcephaly (MCPH): a review of clinical, molecular, and evolutionary findings ' (2005 ) 76 Am. J. Hum. Genet. : 717 -728.

    • Search Google Scholar
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