1. Two patients with interstitial del(14q), one with features of the Holt-Oram syndrome. Exclusion mapping of PI (alpha-1- antitrypsin);Turleau, C.; de Grouchy, J.; Chavin-Colin, F.;Ann Genet (Paris),1984
2. Deletion 14q(q24.3 to q32. 1) syndrome: significance of peculiar facial appearance in its diagnosis, and deletion mapping of PI (alpha 1-antitrypsin);Yamamoto, Y.; Sawa, R.; Okamoto, N.; Matsui, A.; Yanagisawa, M.; Ikemoto, S.;Hum Genet,1986
3. A child with multiple congenital anomalies and karyotype 46, XY, del(l4)(q31q32. 3): further delineation of chromosome 14 interstitial deletion syndrome;Gorski, J.L.; Uhlmann, W.R.; Glover, T.W.;Am J Hum Genet,1990
4. A case of deletion 14(q22.1-q22.3) associated with anophthalmia and pituitary abnormalities;Elliott, J.; Maltby, E.L.; Reynolds, B.;J Med Genet,1993
5. Molecular analysis of three patients with interstitial deletions of chromosome band 14q31;Byth, B.C.; Costa, M.T.; Teshima, I.E.; Wilson, W.G.; Carter, N.P.; Cox, D.W.;Jf Med Genet,1995