Two cases of partial trisomy 8p and partial monosomy 21q in a family with a reciprocal translocation (8;21)(p21.1;q22.3).

Author:

Plomp A S,Engelen J J,Albrechts J C,de Die-Smulders C E,Hamers A J

Publisher

BMJ

Subject

Genetics(clinical),Genetics

Reference37 articles.

1. Inverted duplication of 8p: ten new patients and review of the literature;Feldman, G.; Weiss, L.; Phelan, M.C.; Schroer, R.J.; van Dyke, D.L.;AmJMed Genet,1993

2. Clinical and cytogenetic findings in seven cases of inverted duplication of 8p with evidence of a telomeric deletion using fluorescence in situ hybridization;Guo, W.J.; Callif-Daley, F.; Zapata, M.C.; Miller, M.E.;Am J Med Genet,1995

3. Partial duplication 8p due to interstitial duplication: inv dup(8) (p21.1-*p22);Kleczkowska, A.; Fryns, J.P.; D'Hondt, F.; Jaeken, J.; van den Berghe, H.;Ann Genet,1987

4. Familial partial trisomy 8p without dysmorphic features and only mild mental retardation;Engelen, J.J.M.; de Die-Smulders, C.E.M.; Sijstermans, J.M.J.; Meers, L.E.C.; Albrechts, J.C.M.; Hamers, A.J.H.;JMed Genet,1995

5. Inversion duplication of the short arm of chromosome 8: clinical data on seven patients and review of the literature;de Die-Smulders CEM; JJM, Engelen; CTRM, Schrander-Stumpel;Am J Med Genet,1995

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