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Tom Strachan

Veröffentlichungen von Tom Strachan zu Strachan, David ->
weitere Veröffentlichungen von Tom Strachan:
Human embryo use in developmental research (1995)
Highly polymorphic dinucleotide repeat at the NF2 gene (1995)
A de novo pathological point mutation at the 21–hydroxylase locus: implications for gene conversion in the human genome (1993)
A new dimension for the human genome project: towards comprehensive expression maps (1997)
Restriction fragment length polymorphism at the HLA-C locus (1987)
Waardenburg's syndrome patients have mutations in the human homologue of the Pax-3 paired box gene (1992)
Mutations in the PAX3 gene causing Waardenburg syndrome type 1 and type 2 (1993)
NIPBL, encoding a homolog of fungal Scc2-type sister chromatid cohesion proteins and fly Nipped-B, is mutated in Cornelia de Lange syndrome (2004)
The HLA-AW24 gene: Sequence, surroundings and comparison with the HLA-A2 and HLA-A3 genes (1985)
Molecular analysis of the human MHC class I region in hereditary haemochromatosis (1990)
Extended MHC haplotypes and CYP21/C4 gene organisation in Irish 21-hydroxylase deficiency families (1991)
CYP21/C4 gene organisation in Italian 21-hydroxylase deficiency families (1992)
Eleven novel mutations in the NF2 tumour suppressor gene (1995)
An HLA-C-specific DNA probe (1986)
A gene for autosomal dominant sacral agenesis maps to the holoprosencephaly region at 7q36 (1995)
Veröffentlichungen zu Strachan, David
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1
Bourn, David, Strachan, Tom Highly polymorphic dinucleotide repeat at the NF2 gene
in: Human genetics , ISSN 1432-1203, Vol. 95 (6. 1995), p. 712-712
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1995
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2
Bourn, David, Evans, Gareth, ... Eleven novel mutations in the NF2 tumour suppressor gene
in: Human genetics , ISSN 1432-1203, Vol. 95 (5. 1995), p. 572-574
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1995
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3
Strachan, Tom, Dodge, Alan B., ... An HLA-C-specific DNA probe
in: Immunogenetics , ISSN 1432-1211, Vol. 23 (2. 1986), p. 115-120
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1986
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4
Burke, John P., Orton, Helen P., ... Whiplash and its effect on the visual system
in: Graefe's archive for clinical and experimental ophthalmology , ISSN 1435-702X, Vol. 230 (4. 1992), p. 335-339
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1992
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5
Karmali, Mohamed A., Arbus, Gerald S., ... A family outbreak of hemolytic-uremic syndrome associated with verotoxin-producingEscherichia coli serotype 0157:H7
in: Pediatric nephrology , ISSN 1432-198X, Vol. 2 (4. 1988), p. 409-414
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1988
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6
Morgan, David, Turnpenny, Lee, ... Inversin, a novel gene in the vertebrate left-right axis pathway, ispartially deleted in the inv mouse
in: Nature genetics . - New York, NY : Nature America, ISSN 1546-1718, Vol. 20, No. 2 (1998), p. 149-156
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1998
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7
Yi Li, Quan, Newbury-Ecob, Ruth A., ... Holt-Oram syndrome is caused by mutations in TBX5, a member of the Brachyury (T) gene family
in: Nature genetics . - New York, NY : Nature America, ISSN 1546-1718, Vol. 15, No. 1 (1997), p. 21-29
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1997
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8
Smyth, Deborah J, Howson, Joanna M M, ... Assessing the validity of the association between the SUMO4 M55V variant and risk of type 1 diabetes
in: Nature genetics . - New York, NY : Nature America, ISSN 1546-1718, Vol. 37, No. 2 (2005), p. 110-111
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2005
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9
Thomson, Wendy, Barton, Anne, ... Rheumatoid arthritis association at 6q23
in: Nature genetics . - New York, NY : Nature America, ISSN 1546-1718, Vol. 39, No. 12 (2007), p. 1431-1433
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2007
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10
Ross, Alison J., Ruiz-Perez, Victor, ... A homeobox gene, HLXB9, is the major locus for dominantly inheritedsacral agenesis
in: Nature genetics . - New York, NY : Nature America, ISSN 1546-1718, Vol. 20, No. 4 (1998), p. 358-361
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1998
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11
Moffatt, Miriam F., Kabesch, Michael, ... Genetic variants regulating ORMDL3 expression contribute to the risk of childhood asthma
in: Nature . - London [u.a.] : Nature Publising Group, ISSN 1476-4687, Vol. 448, No. 7152 (2007), p. 470-473
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2007
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12
Parkes, Miles, Barrett, Jeffrey C, ... Sequence variants in the autophagy gene IRGM and multiple other replicating loci contribute to Crohn's disease susceptibility
in: Nature genetics . - New York, NY : Nature America, ISSN 1546-1718, Vol. 39, No. 7 (2007), p. 830-832
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2007
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13
Burton, Paul R, Clayton, David G, ... Association scan of 14,500 nonsynonymous SNPs in four diseases identifies autoimmunity variants
in: Nature genetics . - New York, NY : Nature America, ISSN 1546-1718, Vol. 39, No. 11 (2007), p. 1329-1337
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2007
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14
Nejentsev, Sergey, Howson, Joanna M. M., ... Localization of type 1 diabetes susceptibility to the MHC class I genes HLA-B and HLA-A
in: Nature . - London [u.a.] : Nature Publising Group, ISSN 1476-4687, Vol. 450, No. 7171 (2007), p. 887-892
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2007
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15
Burton, Paul R., Clayton, David G., ... Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls
in: Nature . - London [u.a.] : Nature Publising Group, ISSN 1476-4687, Vol. 447, No. 7145 (2007), p. 661-678
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2007