Molecular characterisation of chromosome 4p deletions resulting in Wolf-Hirschhorn syndrome.

Por Estabrooks, L L, Lamb, A N, Aylsworth, A S, Callanan, N P, Rao, K W
Publicado em 1994

A molecular deletion of distal chromosome 4p in two families with a satellited chromosome 4 lacking the Wolf-Hirschhorn syndrome phenotype.

Por Estabrooks, L L, Lamb, A N, Kirkman, H N, Callanan, N P, Rao, K W
Publicado em 1992

Subtelomere FISH analysis of 11 688 cases: an evaluation of the frequency and pattern of subtelomere rearrangements in individuals with developmental disabilities

Por Ravnan, J B, Tepperberg, J H, Papenhausen, P, Lamb, A N, Hedrick, J, Eash, D, Ledbetter, D H, Martin, C L
Publicado em 2006

Refinement of the Region for Split Hand/Foot Malformation 5 on 2q31.1

Por Theisen, A., Rosenfeld, J.A., Shane, K., McBride, K.L., Atkin, J.F., Gaba, C., Hoo, J., Kurczynski, T.W., Schnur, R.E., Coffey, L.B., Zackai, E.H., Schimmenti, L., Friedman, N., Zabukovec, M., Ball, S., Pagon, R., Lucas, A., Brasington, C.K., Spence, J.E., Sparks, S., Banks, V., Smith, W., Friedberg, T., Wyatt, P.R., Aust, M., Tervo, R., Crowley, A., Skidmore, D., Lamb, A.N., Ravnan, B., Sahoo, T., Schultz, R., Torchia, B.S., Sgro, M., Chitayat, D., Shaffer, L.G.
Publicado em 2011