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Results: 5

Authors: LI QY NEWBURYECOB RA TERRETT JA WILSON DI CURTIS ARJ YI CH GEBUHR T BULLEN PJ ROBSON SC STRACHAN T BONNET D LYONNET S YOUNG ID RAEBURN JA BUCKLER AJ LAW DJ BROOK JD
Citation: Qy. Li et al., HOLT-ORAM SYNDROME IS CAUSED BY MUTATIONS IN TBX5, A MEMBER OF THE BRACHYURY (T) GENE FAMILY, Nature genetics, 15(1), 1997, pp. 21-29

Authors: BUI TD LAKO M LEJEUNE S CURTIS ARJ STRACHAN T LINDSAY S HARRIS AL
Citation: Td. Bui et al., ISOLATION OF A FULL-LENGTH HUMAN WNT7A GENE IMPLICATED IN LIMB DEVELOPMENT AND CELL-TRANSFORMATION, AND MAPPING TO CHROMOSOME 3P25, Gene, 189(1), 1997, pp. 25-29

Authors: LAKO M STRACHAN T CURTIS ARJ LINDSAY S
Citation: M. Lako et al., ISOLATION AND CHARACTERIZATION OF WNT8B, A NOVEL HUMAN WNT GENE THAT MAPS TO 10Q24, Genomics, 35(2), 1996, pp. 386-388

Authors: THISELTON DL KAMAKARI S CURTIS ARJ COLEMAN MP DAVIES KE LINDSAY S BHATTACHARYA S
Citation: Dl. Thiselton et al., DINUCLEOTIDE REPEAT POLYMORPHISM AT THE DXS556 LOCUS, Human molecular genetics, 2(5), 1993, pp. 613-613

Authors: LINDSAY S CURTIS ARJ ROUSTAN P KAMAKARI S THISELTON DL STEPHENSON A BHATTACHARYA SS
Citation: S. Lindsay et al., ISOLATION AND CHARACTERIZATION OF 3 MICROSATELLITE MARKERS IN THE PROXIMAL LONG ARM OF THE HUMAN X-CHROMOSOME, Genomics, 17(1), 1993, pp. 208-210
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