Authors:
Li, M
Squire, J
Shuman, C
Fei, YL
Atkin, J
Pauli, R
Smith, A
Nishikawa, J
Chitayat, D
Weksberg, R
Citation: M. Li et al., Imprinting status of 11p15 genes in Beckwith-Wiedemann syndrome patients with CDKN1C mutations (vol 74, pg 370, 2001), GENOMICS, 77(1-2), 2001, pp. 115-115
Authors:
Li, M
Squire, J
Shuman, C
Atkin, J
Pauli, R
Smith, A
Chitayat, D
Weksberg, R
Citation: M. Li et al., Imprinting status of 11p15 genes in Beckwith-Wiedemann syndrome patients with CDKN1C mutations, GENOMICS, 74(3), 2001, pp. 370-376
Authors:
Li, M
Shuman, C
Fei, YL
Cutiongco, E
Bender, HA
Stevens, C
Wilkins-Haug, L
Day-Salvatore, D
Yong, SL
Geraghty, MT
Squire, J
Weksberg, R
Citation: M. Li et al., GPC3 mutation analysis in a spectrum of patients with overgrowth expands the phenotype of Simpson-Golabi-Behmel syndrome, AM J MED G, 102(2), 2001, pp. 161-168
Authors:
Ciray, HN
Fu, X
Olovsson, M
Ahlsen, G
Shuman, C
Lindblom, B
Ulmsten, U
Citation: Hn. Ciray et al., Presence and localization of connexins 43 and 26 in cell cultures derived from myometrial tissues from nonpregnant and pregnant women and from leiomyomas, AM J OBST G, 182(4), 2000, pp. 926-930