1. The DiGeorge anomaly as a de- Prevalence of 22ql 1 microdeletions in DiGeorge and velocardiofacial syndromes velopmental field defect;Lammer, E.J.; Opitz, J.M.;Am J Med Genet,1986
2. Partial monosomy 22pter--11 in a newborn with the clinical features of trisomy 13 syndrome;Back, E.; Stier, R.; Bohsen, N.; Adlung, A.; Hameister, H.;Ann Genet (Paris),1980
3. Aula 0. A deletion in chromosome 22 can cause DiGeorge syndrome;la Chapelle A, De; R, Herva; M, Koivisto;Hum Genet,1981
4. The association of the DiGeorge anomalad with partial monosomy of chromosome 22;Kelley, R.I.; Zackai, E.H.; Emanuel, B.S.; Kistenmacher, M.; Greenberg, F.; Punnett, H.;J Pediatr,1982
5. Familial DiGeorge syndrome and associated partial monosomy of chromosome 22;Greenberg, F.; Crowder, W.E.; Paschall, V.; J-, Colon-Linares; C, Lubianski; B, Ledbetter; D.H.;Hum Genet,1984