1. Cytogenetic findings in a prospective series of patients with DiGeorge anomaly;Greenberg, F.; Elder, F.F.B.; Haffner, P.; Nothrup, H.; Ledbetter, D.;Am ]f Hum Genet,1988
2. Microdeletions within 22ql 1 associated with sporadic and familial DiGeorge syndrome;Scambler, P.J.; Carey, A.H.; Wyse, R.K.H.;Genomics,1991
3. Interstitial deletions in DiGeorge syndrome detected with microclones from 22ql 1;Carey, A.H.; Claussen, U.; Ludecke, H.J.,1992
4. A genetic etiology for DiGeorge syndrome: consistent deletions and microdeletions of 22q I 1;Driscoll, D.A.; Budarf, M.L.; Emanuel, B.;Am J Hum Genet,1992
5. Molecular genetic study of the frequency of monosomy 22ql 1 in DiGeorge syndrome;Carey, A.H.; Kelly, D.; Halford, S.;Am 7 Hum Genet,1992