1. Meiotic analysis of a pericentric inversion, inv (7)(p22q32), in the father of a child with a duplication-deletion of chromosome 7;Winsor, E.J.T.; Palmer, C.G.; Ellis, P.M.; Hunter, J.L.P.; FergusonSmith, M.A.;Cytogenet Cell Genet,1978
2. Emerging phenotype of duplication ( 7p): a report of three cases and review of the literature;Milunsky, J.M.; Wyandt, H.E.; Milunsky, A.;Am J Med,1989
3. Partial trisomy of the short arm of chromosome 7 due to a familial translocation rcp (7; 14Xpll;Carnevale, A.; Frias, S.; del Castillo, V.,1978
4. Duplication 7p in a family with t(7; 11): association with anomalies of the anterior cranial base;Odell, J.M.; Siebert, JR, Bradley; C, Salk; D.;Am J Med Genet,1987
5. Duplication 7p de novo and literature review;Zerres, K.; Schwanitz, G.; Gellissen, K.; Schoers, L.; Sohler, R.;Ann Genet (Paris),1989