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T.C Gilliam

Veröffentlichungen von T.C Gilliam zu Gilliam, T.C. ->
weitere Veröffentlichungen von T.C Gilliam:
The positions of three restriction fragment length polymorphisms on chromosome 4 relative to known genetic markers (1984)
A Microsatellite Genetic Linkage Map of Human Chromosome 18 (1993)
Preliminary linkage analysis of schizophrenia in Canadian pedigrees to a candidate region on chromosome 5 (1989)
Isolation and characterization of a highly polymorphic human locus (DXS455) in proximal Xq28 (1992)
Deletion mapping of DNA markers to a region of chromosome 5 that cosegregates with schizophrenia (1989)
Genetic homogeneity between acute and chronic forms of spinal muscular atrophy (1990)
A somatic cell hybrid panel for localizing DNA segments near the Huntington's disease gene (1987)
Refinement of the Spinal Muscular Atrophy Locus to the Interval between D5S435 and MAP1B (1993)
An Investigation of Genetic Heterogeneity and Linkage Disequilibrium in 161 Families with Spinal Muscular Atrophy (1994)
A Microsatellite Genetic Linkage Map of Human Chromosome 13 (1993)
Genetic mapping of chronic childhood-onset spinal muscular atrophy to chromosome 5q1 1.2Â13.3 (1990)
Mapping, cloning and genetic characterization of the region containing the Wilson disease gene (1993)
Linkage analysis of spinal muscular atrophy (1992)
Synteny on mouse chromosome 5 of homologs for human DNA loci linked to the Huntington disease gene (1989)
Physical maps of 4p16.3, the area expected to contain the Huntington disease mutation (1990)
Veröffentlichungen zu Gilliam, T.C.
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1
Gilliam, T. C., Scambler, P., ... The positions of three restriction fragment length polymorphisms on chromosome 4 relative to known genetic markers
in: Human genetics , ISSN 1432-1203, Vol. 68 (2. 1984), p. 154-158
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1984
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2
Straub, R.E., Speer, M.C., ... A Microsatellite Genetic Linkage Map of Human Chromosome 18
in: Genomics, in: Genomics . - Amsterdam : Elsevier, ISSN 0888-7543, ZDB-ID 1468023-3 Vol. 15, No. 1 (1993), p. 48-56
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1993
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3
Bassett, A.S., Sandkuyl, L., ... Preliminary linkage analysis of schizophrenia in Canadian pedigrees to a candidate region on chromosome 5
in: Schizophrenia Research, in: Schizophrenia Research . - Amsterdam : Elsevier, ISSN 0920-9964, ZDB-ID 1500726-1 Vol. 2, No. 1-2 (1989), p. 40
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1989
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4
Consalez, G.G., Stayton, C.L., ... Isolation and characterization of a highly polymorphic human locus (DXS455) in proximal Xq28
in: Genomics, in: Genomics . - Amsterdam : Elsevier, ISSN 0888-7543, ZDB-ID 1468023-3 Vol. 12, No. 4 (1992), p. 710-714
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1992
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5
Gilliam, T.C., Freimer, N.B., ... Deletion mapping of DNA markers to a region of chromosome 5 that cosegregates with schizophrenia
in: Genomics, in: Genomics . - Amsterdam : Elsevier, ISSN 0888-7543, ZDB-ID 1468023-3 Vol. 5, No. 4 (1989), p. 940-944
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1989
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6
Gilliam, T. C., Brzustowicz, L. M., ... Genetic homogeneity between acute and chronic forms of spinal muscular atrophy
in: Nature . - London [u.a.] : Nature Publising Group, ISSN 1476-4687, Vol. 345, No. 6278 (1990), p. 823-825
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1990
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7
MacDonald, M.E., Anderson, M.A., ... A somatic cell hybrid panel for localizing DNA segments near the Huntington's disease gene
in: Genomics, in: Genomics . - Amsterdam : Elsevier, ISSN 0888-7543, ZDB-ID 1468023-3 Vol. 1, No. 1 (1987), p. 29-34
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1987
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8
Soares, V.M., Brzustowicz, L.M., ... Refinement of the Spinal Muscular Atrophy Locus to the Interval between D5S435 and MAP1B
in: Genomics, in: Genomics . - Amsterdam : Elsevier, ISSN 0888-7543, ZDB-ID 1468023-3 Vol. 15, No. 2 (1993), p. 365-371
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1993
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9
Merette, C., Brzustowicz, L.M., ... An Investigation of Genetic Heterogeneity and Linkage Disequilibrium in 161 Families with Spinal Muscular Atrophy
in: Genomics, in: Genomics . - Amsterdam : Elsevier, ISSN 0888-7543, ZDB-ID 1468023-3 Vol. 21, No. 1 (1994), p. 27-33
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1994
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10
Petrukhin, K.E., Speer, M.C., ... A Microsatellite Genetic Linkage Map of Human Chromosome 13
in: Genomics, in: Genomics . - Amsterdam : Elsevier, ISSN 0888-7543, ZDB-ID 1468023-3 Vol. 15, No. 1 (1993), p. 76-85
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1993
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11
Brzustowicz, L. M., Lehner, T., ... Genetic mapping of chronic childhood-onset spinal muscular atrophy to chromosome 5q1 1.2Â13.3
in: Nature . - London [u.a.] : Nature Publising Group, ISSN 1476-4687, Vol. 344, No. 6266 (1990), p. 540-541
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1990
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12
Petrukhin, K., Fischer, S. G., ... Mapping, cloning and genetic characterization of the region containing the Wilson disease gene
in: Nature genetics . - New York, NY : Nature America, ISSN 1546-1718, Vol. 5, No. 4 (1993), p. 338-343
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1993
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13
Daniels, R.J., Thomas, N.H., ... Linkage analysis of spinal muscular atrophy
in: Genomics, in: Genomics . - Amsterdam : Elsevier, ISSN 0888-7543, ZDB-ID 1468023-3 Vol. 12, No. 2 (1992), p. 335-339
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1992
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14
Cheng, S.V., Martin, G.R., ... Synteny on mouse chromosome 5 of homologs for human DNA loci linked to the Huntington disease gene
in: Genomics, in: Genomics . - Amsterdam : Elsevier, ISSN 0888-7543, ZDB-ID 1468023-3 Vol. 4, No. 3 (1989), p. 419-426
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1989
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15
Bucan, M., Zimmer, M., ... Physical maps of 4p16.3, the area expected to contain the Huntington disease mutation
in: Genomics, in: Genomics . - Amsterdam : Elsevier, ISSN 0888-7543, ZDB-ID 1468023-3 Vol. 6, No. 1 (1990), p. 1-15
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1990
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16
Brzustowicz, L.M., Kleyn, P.W., ... Fine-mapping of the spinal muscular atrophy locus to a region flanked by MAP1B and D5S6
in: Genomics, in: Genomics . - Amsterdam : Elsevier, ISSN 0888-7543, ZDB-ID 1468023-3 Vol. 13, No. 4 (1992), p. 991-998
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1992
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17
Tanzi, R.E., Petrukhin, K., ... The Wilson disease gene is a copper transporting ATPase with homology to the Menkes disease gene
in: Nature genetics . - New York, NY : Nature America, ISSN 1546-1718, Vol. 5, No. 4 (1993), p. 344-350
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1993