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Annales De Genetique|January 1, 1988
A further 46,XYp- femaleH Rivera, M Moller, L M Baltazar, et al.Annales De Genetique|January 1, 1988
A case of monosomy 21B Garzicić, M Guć-Sćekić, G Pilić-Radivojević, et al.Annales De Genetique|January 1, 1988
Partial duplication of 17 long armE Lenzini, A Leszl, L Artifoni, et al.Annales De Genetique|January 1, 1988
The fetal phenotype in 15q2 duplicationJ P Fryns, A Kleczkowska, P Moerman, et al.Annales De Genetique|January 1, 1988
Cytogenetic analysis of 570 first trimester chorionic villi samplings: technique and resultsM Jotterand-Bellomo, G Pescia, H Nguyen The, et al.Annales De Genetique|January 1, 1988
Chromosomal localization of a bovine male specific probeC P Popescu, C Cotinot, J Boscher, et al.Annales De Genetique|January 1, 1988
Three large Danish families with a paracentric inversion in the short arm of chromosome N. 5K Baggesen, U Friedrich, P K Jensen, et al.Annales De Genetique|January 5, 2002
Second trimester prenatal diagnosis of epignathus teratoma in ring X chromosome mosaicism with inactive ring X chromosomeI Witters, P Moerman, D Louwagie, et al.Annales De Genetique|January 5, 2002
Deletion screening by fluorescence in situ hybridization in Rett syndrome patientsV Bourdon, C Philippe, A Grandemenge, et al.Annales De Genetique|January 5, 2002
Contribution of ultrasonographic examination to the prenatal detection of chromosomal abnormalities in 19 centres across EuropeC De Vigan, N Baena, E Cariati, et al.Pageof 129