Newborn screening for hemoglobinopathies: the benefit beyond the target.

Por Grover, R, Newman, S, Wethers, D, Anyane-Yeboa, K, Pass, K
Publicado em 1986

Coding mutations in p57KIP2 are present in some cases of Beckwith-Wiedemann syndrome but are rare or absent in Wilms tumors.

Por O'Keefe, D, Dao, D, Zhao, L, Sanderson, R, Warburton, D, Weiss, L, Anyane-Yeboa, K, Tycko, B
Publicado em 1997

Molecular definition of 22q11 deletions in 151 velo-cardio-facial syndrome patients.

Por Carlson, C, Sirotkin, H, Pandita, R, Goldberg, R, McKie, J, Wadey, R, Patanjali, S R, Weissman, S M, Anyane-Yeboa, K, Warburton, D, Scambler, P, Shprintzen, R, Kucherlapati, R, Morrow, B E
Publicado em 1997

DAX1 mutations map to putative structural domains in a deduced three-dimensional model.

Por Zhang, Y H, Guo, W, Wagner, R L, Huang, B L, McCabe, L, Vilain, E, Burris, T P, Anyane-Yeboa, K, Burghes, A H, Chitayat, D, Chudley, A E, Genel, M, Gertner, J M, Klingensmith, G J, Levine, S N, Nakamoto, J, New, M I, Pagon, R A, Pappas, J G, Quigley, C A, Rosenthal, I M, Baxter, J D, Fletterick, R J, McCabe, E R
Publicado em 1998