Authors:
Marsh, DJ
Kum, JB
Lunetta, KL
Bennett, MJ
Gorlin, RJ
Ahmed, SF
Bodurtha, J
Crowe, C
Curtis, MA
Dasouki, M
Dunn, T
Feit, H
Geraghty, MT
Graham, JM
Hodgson, SV
Hunter, A
Korf, BR
Manchester, D
Miesfeldt, S
Murday, VA
Nathanson, KL
Parisi, M
Pober, B
Romano, C
Tolmie, JL
Trembath, R
Winter, RM
Zackai, EH
Zori, RT
Weng, LP
Dahia, PLM
Eng, C
Citation: Dj. Marsh et al., PTEN mutation spectrum and genotype-phenotype correlations in Bannayan-Riley-Ruvalcaba syndrome suggest a single entity with Cowden syndrome, HUM MOL GEN, 8(8), 1999, pp. 1461-1472
Authors:
Freedenberg, DL
Gane, LW
Richards, CS
Lampe, M
Hills, J
O'Connor, R
Manchester, D
Taylor, A
Tassone, F
Hulseberg, D
Hagerman, RJ
Patil, SR
Citation: Dl. Freedenberg et al., Fragile X syndrome and an isodicentric X chromosome in a woman with multiple anomalies, developmental delay, and normal pubertal development, AM J MED G, 85(3), 1999, pp. 197-201
Authors:
Marcus, AC
Ahnen, D
Cutter, G
Calonge, N
Russell, S
Sedlacek, SM
Wood, M
Manchester, D
Fox, L
McCaskill-Stevens, W
Fairclough, D
Hines, S
Wenzel, L
Osborn, K
Citation: Ac. Marcus et al., Promoting cancer screening among the first-degree relatives of breast and colorectal cancer patients: The design of two randomized trials, PREV MED, 28(3), 1999, pp. 229-242