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Results: 1-10 |
Results: 10
Inheritance of osteosarcoma and Paget's disease of bone - A familial loss of heterozygosity study
Authors: McNairn, JDK Damron, TA Landas, SK Ambrose, JL Shrimpton, AE
Citation: Jdk. Mcnairn et al., Inheritance of osteosarcoma and Paget's disease of bone - A familial loss of heterozygosity study, J MOL DIAGN, 3(4), 2001, pp. 171-177
A PCR assay for detecting clonal rearrangement of the TCR-gamma gene
Authors: Lamberson, C Hutchison, RE Shrimpton, AE
Citation: C. Lamberson et al., A PCR assay for detecting clonal rearrangement of the TCR-gamma gene, MOL DIAGN, 6(2), 2001, pp. 117-124
Syndrome of short stature, widow's peak, ptosis, posteriorly angulated ears, and joint problems: Exclusion of the aarskog (FGD1) gene as a candidate gene
Authors: LaDine, BJ Simmons, JA Shrimpton, AE Hoo, JJ
Citation: Bj. Ladine et al., Syndrome of short stature, widow's peak, ptosis, posteriorly angulated ears, and joint problems: Exclusion of the aarskog (FGD1) gene as a candidate gene, AM J MED G, 99(3), 2001, pp. 248-251
Cognitive deficits associated with a recently reported familial neurodegenerative disease - Familial encephalopathy with neuroserpin inclusion bodies
Authors: Bradshaw, CB Davis, RL Shrimpton, AE Holohan, PD Rea, CB Fieglin, D Kent, P Collins, GH
Citation: Cb. Bradshaw et al., Cognitive deficits associated with a recently reported familial neurodegenerative disease - Familial encephalopathy with neuroserpin inclusion bodies, ARCH NEUROL, 58(9), 2001, pp. 1429-1434
R117H and IVS8-5T cystic fibrosis mutation detection by restriction enzymedigestion
Authors: Shrimpton, AE
Citation: Ae. Shrimpton, R117H and IVS8-5T cystic fibrosis mutation detection by restriction enzymedigestion, MOL DIAGN, 5(3), 2000, pp. 235-238
Narrowing the map of a gene (MRXS9) for X-linked mental retardation, microcephaly, and variably short stature at Xq12-q21.31
Authors: Shrimpton, AE Braddock, BR Hoo, JJ
Citation: Ae. Shrimpton et al., Narrowing the map of a gene (MRXS9) for X-linked mental retardation, microcephaly, and variably short stature at Xq12-q21.31, AM J MED G, 92(2), 2000, pp. 155-156
Association for molecular pathology statement - Recommendations for in-house development and operation of molecular diagnostic tests
Authors: Whittaker, MH Farkas, DH Kaul, KL Shrimpton, AE Leonard, DGB
Citation: Mh. Whittaker et al., Association for molecular pathology statement - Recommendations for in-house development and operation of molecular diagnostic tests, AM J CLIN P, 111(4), 1999, pp. 449-463
Mapping of a gene (MRXS9) for X-linked mental Retardation, microcephaly, and variably short stature to Xq12-q21.31
Authors: Shrimpton, AE Daly, KM Hoo, JJ
Citation: Ae. Shrimpton et al., Mapping of a gene (MRXS9) for X-linked mental Retardation, microcephaly, and variably short stature to Xq12-q21.31, AM J MED G, 84(3), 1999, pp. 293-299
Familial dementia caused by polymlerization of mutant neurosergin
Authors: Davis, RL Shrimpton, AE Holohan, PD Bradshaw, C Feiglin, D Collins, GH Sonderegger, P Kinter, J Becker, LM Lacbawan, F Krasnewich, D Muenke, M Lawrence, DA Yerby, MS Shaw, CM Gooptu, B Elliott, PR Finch, JT Carrell, RW Lomas, DA
Citation: Rl. Davis et al., Familial dementia caused by polymlerization of mutant neurosergin, NATURE, 401(6751), 1999, pp. 376-379
Familiar encephalopathy with neuroserpin inclusion bodies
Authors: Davis, RL Holohan, PD Shrimpton, AE Tatum, AH Daucher, J Collins, GH Todd, R Bradshaw, C Kent, P Feiglin, D Rosenbaum, A Yerby, MS Shaw, CM Lacbawan, F Lawrence, DA
Citation: Rl. Davis et al., Familiar encephalopathy with neuroserpin inclusion bodies, AM J PATH, 155(6), 1999, pp. 1901-1913
Risultati: 1-10 |