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Results:
1-10
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Results: 10
Authors:
Schofield, PN
Joyce, JA
Lam, WK
Grandjean, V
Ferguson-Smith, A
Reik, W
Maher, ER
Citation: Pn. Schofield et al., Genomic imprinting and cancer; new paradigms in the genetics of neoplasia, TOX LETT, 120(1-3), 2001, pp. 151-160
Authors:
Kocialkowski, S
Yeger, H
Kingdom, J
Perbal, B
Schofield, PN
Citation: S. Kocialkowski et al., Expression of the human NOV gene in first trimester fetal tissues, ANAT EMBRYO, 203(6), 2001, pp. 417-427
Authors:
Martinerie, C
Gicquel, C
Louvel, A
Laurent, M
Schofield, PN
Le Bouc, Y
Citation: C. Martinerie et al., Altered expression of novH is associated with human adrenocortical tumorigenesis, J CLIN END, 86(8), 2001, pp. 3929-3940
Authors:
Natarajan, D
Andermarcher, E
Schofield, PN
Boulter, CA
Citation: D. Natarajan et al., Mouse Nov gene is expressed in hypaxial musculature and cranial structuresderived from neural crest cells and placodes, DEV DYNAM, 219(3), 2000, pp. 417-423
Authors:
Grandjean, V
Smith, J
Schofield, PN
Ferguson-Smtih, AC
Citation: V. Grandjean et al., Increased IGF-II protein affects p57(kip2) expression in vivo and in vitro: Implications for Beckwith-Wiedemann syndrome, P NAS US, 97(10), 2000, pp. 5279-5284
Authors:
Catchpoole, D
Smallwood, AV
Joyce, JA
Murrell, A
Lam, W
Tang, T
Munroe, D
Reik, W
Schofield, PN
Maher, ER
Citation: D. Catchpoole et al., Mutation analysis of H19 and NAP1L4 (hNAP2) candidate genes and IGF2 DMR2 in Beckwith-Wiedemann syndrome, J MED GENET, 37(3), 2000, pp. 212-215
Authors:
Engel, JR
Smallwood, A
Harper, A
Higgins, MJ
Oshimura, M
Reik, O
Schofield, PN
Maher, ER
Citation: Jr. Engel et al., Epigenotype-phenotype correlations in Beckwith-Wiedemann syndrome, J MED GENET, 37(12), 2000, pp. 921-926
Authors:
Smilinich, NJ
Day, CD
Fitzpatrick, GV
Caldwell, GM
Lossie, AC
Cooper, PR
Smallwood, AC
Joyce, JA
Schofield, PN
Reik, W
Nicholls, RD
Weksberg, R
Driscoll, DJ
Maher, ER
Shows, TB
Higgins, MJ
Citation: Nj. Smilinich et al., A maternally methylated CpG island in KvLQT1 is associated with an antisense paternal transcript and loss of imprinting in Beckwith-Wiedemann syndrome, P NAS US, 96(14), 1999, pp. 8064-8069
Authors:
Lam, WWK
Hatada, I
Ohishi, S
Mukai, T
Joyce, JA
Cole, TRP
Donnai, D
Reik, W
Schofield, PN
Maher, ER
Citation: Wwk. Lam et al., Analysis of germline CDKN1C (p57(KIP2)) mutations in familial and sporadicBeckwith-Wiedemann syndrome (BWS) provides a novel genotype-phenotype correlation, J MED GENET, 36(7), 1999, pp. 518-523
Authors:
Schofield, PN
Citation: Pn. Schofield, Impact of genomic imprinting on genomic instability and radiation-induced mutation, INT J RAD B, 74(6), 1998, pp. 705-710
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