Author:
CÓRDOVA-FLETES CARLOS,SÁINZ-GONZÁLEZ ENRIQUE,AVENDAÑO-GÁLVEZ ROBERTO IVÁN,RAMÍREZ-VELAZCO AZUBEL,RIVERA HORACIO,ORTIZ-LÓPEZ ROCÍO,ARÁMBULA-MERAZ ELIAKYM,PICOS-CÁRDENAS VERÓNICA JUDITH
Publisher
Springer Science and Business Media LLC
Reference17 articles.
1. Boghosian-Sell L., Mewar R., Harrison W., Shapiro R. M., Zackai E. H., Carey J. et al. 1994 Molecular mapping of the Edwards syndrome phenotype to two noncontiguous regions on chromosome 18. Am. J. Hum. Genet. 55, 476–483.
2. Cody J. D., Heard P. L., Crandall A. C., Carter E. M., Li J., Hardies L. J. et al. 2009 Narrowing critical regions and determining penetrance for selected 18q−phenotypes. Am. J. Med. Genet. A 149A, 1421–1430.
3. Courtens W., Grossman D., Van Roy N., Messiaen L., Vamos E., Toppet V., et al. 1998 Noonan-like phenotype in monozygotic twins with a duplication-deficiency of the long arm of chromosome 18 resulting from a maternal paracentric inversion. Hum. Genet. 103, 497–505.
4. Debacker K., Winnepenninckx B., Ben-Porat N., FitzPatrick D., Van Luijk R., Scheers S., et al. 2007 FRA18C: a new aphidicolin-inducible fragile site on chromosome 18q22, possibly associated with in vivo chromosome breakage. J. Med. Genet. 44, 347–352.
5. Feenstra I., Vissers L. E., Orsel M., van Kessel A. G., Brunner H. G., Veltman J. A. et al. 2007 Genotype–phenotype mapping of chromosome 18q deletions by high-resolution array CGH: an update of the phenotypic map. Am. J. Med. Genet. A 143A, 1858–1867.
Cited by
2 articles.
订阅此论文施引文献
订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献