1. A child with multiple congenital anomalies and karyotype 46, XY, del(14) (q31q32. 3): further delineation of chromosome 14 interstitial deletion syndrome;Gorski, J.L.; Uhlmann, W.R.; Glover, T.W.;Am J Hum Genet,1990
2. Deletion (14) (q24. 3q32.1): evidence for a distinct clinical phenotype;Karnitis, S.A.; Bums, K.; Sudduth, K.W.; Golden, W.L.; Wilson, W.G.;Am J Med Genet,1992
3. Opposite imbalances of distal 14q in two unrelated patients;Rivera, H.; Ramirez-Duenas, M.L.; Figuera, L.E.; GonzalezMontes, R.M.; Vasques, A.I.;Ann Genet (Paris),1992
4. A terminal deletion (14) (q3 1.1) in a child with microcephaly, narrow palate, gingival hypertrophy, protuberant ears and mild mental retardation;Yen, F.S.; Podruch, P.E.; Weisskopf, B.;J Med Genet,1989
5. Molecular analysis redefines three human chromosome 14 deletions. Hum Genet;Wintle, R.F.; Costa, T.; Haslam, R.H.A.; Teshima, I.E.; Cox, D.W.