Author:
Bicknell Louise S,Bongers Ernie M H F,Leitch Andrea,Brown Stephen,Schoots Jeroen,Harley Margaret E,Aftimos Salim,Al-Aama Jumana Y,Bober Michael,Brown Paul A J,van Bokhoven Hans,Dean John,Edrees Alaa Y,Feingold Murray,Fryer Alan,Hoefsloot Lies H,Kau Nikolaus,Knoers Nine V A M,MacKenzie James,Opitz John M,Sarda Pierre,Ross Alison,Temple I Karen,Toutain Annick,Wise Carol A,Wright Michael,Jackson Andrew P
Publisher
Springer Science and Business Media LLC
Reference19 articles.
1. Bongers, E.M. et al. Meier-Gorlin syndrome: report of eight additional cases and review. Am. J. Med. Genet. 102, 115–124 (2001).
2. Gorlin, R.J., Cervenka, J., Moller, K., Horrobin, M. & Witkop, C.J. Jr. Malformation syndromes. A selected miscellany. Birth Defects Orig. Artic. Ser. 11, 39–50 (1975).
3. Meier, Z., Poschiavo & Rothschild, M. Case of arthrogryposis multiplex congenita with mandibulofacial dysostosis (Franceschetti syndrome). Helv. Paediatr. Acta. 14, 213–216 (1959).
4. Bicknell, L.S. et al. Mutations in ORC1, encoding the largest subunit of the origin recognition complex, cause microcephalic primordial dwarfism resembling Meier Gorlin syndrome. Nat. Genet. advance online publication, doi:10.1038/ng.776 (27 February 2011).
5. Guernsey, D.L. et al. Mutations in origin recognition complex gene ORC4 cause Meier-Gorlin syndrome. Nat. Genet. advance online publication, doi:10.1038/ng.777 (27 February 2011).
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