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Holger Luthman

Veröffentlichungen von Holger Luthman zu Luthman, Holger ->
weitere Veröffentlichungen von Holger Luthman:
Steroid 21-hydroxylase (P450c21): a new allele and spread of mutations through the pseudogene (1993)
Characterization of mutations on the rare duplicated C4/CYP21 haplotype in steroid 21-hydroxylase deficiency (1994)
A steroid 21-hydroxylase allele concomitantly carrying four disease-causing mutations is not uncommon in the Swedish population (1994)
Spatial distribution of active genes implicated in the regulation of insulin-like growth factor stimulatory loops in human decidual and placental tissue of first-trimester pregnancy (1992)
TaqI HLA-B and -DRB RFLP analysis can predict disease in siblings of affected children with 21-hydroxylase deficiency (1990)
Tight linkage between the Beckwith-Wiedemann syndrome and a microsatellite marker for the TH locus (1993)
DNA haplotype analysis suggests linkage disequilibrium in the human insulin receptor gene (1991)
Localization of the human insulin-like growth-factor-binding protein 4 gene to chromosomal region 17q12–21.1 (1992)
Characterization and chromosomal localization of the human insulin-like growth factor-binding protein 6 gene (1999)
Genetic analysis of non-insulin dependent diabetes mellitus in the GK rat (1996)
A rat genetic linkage map including 67 new microsatellite markers (1999)
MHC2TA is associated with differential MHC molecule expression and susceptibility to rheumatoid arthritis, multiple sclerosis and myocardial infarction (2005)
Veröffentlichungen zu Luthman, Holger
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1
Wedell, Anna, Luthman, Holger Steroid 21-hydroxylase (P450c21): a new allele and spread of mutations through the pseudogene
in: Human genetics , ISSN 1432-1203, Vol. 91 (3. 1993), p. 236-240
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1993
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2
Wedell, Anna, Stengler, Barbro, ... Characterization of mutations on the rare duplicated C4/CYP21 haplotype in steroid 21-hydroxylase deficiency
in: Human genetics , ISSN 1432-1203, Vol. 94 (1. 1994), p. 50-54
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1994
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3
Wedell, Anna, Chun, Xu, ... A steroid 21-hydroxylase allele concomitantly carrying four disease-causing mutations is not uncommon in the Swedish population
in: Human genetics , ISSN 1432-1203, Vol. 93 (2. 1994), p. 204-206
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1994
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4
Glaser, Anna., Luthman, Holger., ... Spatial distribution of active genes implicated in the regulation of insulin-like growth factor stimulatory loops in human decidual and placental tissue of first-trimester...
in: Molecular Reproduction and Development, in: Molecular Reproduction and Development . - New York, NY [u.a.] : Wiley-Liss, ISSN 1040-452X, ZDB-ID 1493888-1 Vol. 33 (1. 1992), p. 7-15
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1992
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5
Olerup, Olle, Luthman, Holger, ... TaqI HLA-B and -DRB RFLP analysis can predict disease in siblings of affected children with 21-hydroxylase deficiency
in: Human genetics , ISSN 1432-1203, Vol. 85 (5. 1990), p. 467-472
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1990
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6
Nordenskjöld, Agneta, Hedborg, Fredrik, ... Tight linkage between the Beckwith-Wiedemann syndrome and a microsatellite marker for the TH locus
in: Human genetics , ISSN 1432-1203, Vol. 92 (3. 1993), p. 296-298
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1993
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7
Sten-Linder, Margareta, Olsson, Marianne, ... DNA haplotype analysis suggests linkage disequilibrium in the human insulin receptor gene
in: Human genetics , ISSN 1432-1203, Vol. 87 (4. 1991), p. 469-474
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1991
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8
Bajalica, Svetlana, Allander, Susanne V., ... Localization of the human insulin-like growth-factor-binding protein 4 gene to chromosomal region 17q12–21.1
in: Human genetics , ISSN 1432-1203, Vol. 89 (2. 1992), p. 234-236
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1992
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9
Ehrenborg, Ewa, Zazzi, Henric, ... Characterization and chromosomal localization of the human insulin-like growth factor-binding protein 6 gene
in: Mammalian genome , ISSN 1432-1777, Vol. 10 (4. 1999), p. 376-380
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1999
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10
Galli, Joakim, Li, Luo-Sheng, ... Genetic analysis of non-insulin dependent diabetes mellitus in the GK rat
in: Nature genetics . - New York, NY : Nature America, ISSN 1546-1718, Vol. 12, No. 1 (1996), p. 31-37
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1996
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11
Fakhrai-Rad, Hossein, Jiao, Hong, ... A rat genetic linkage map including 67 new microsatellite markers
in: Mammalian genome , ISSN 1432-1777, Vol. 10 (11. 1999), p. 1102-1105
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1999
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12
Swanberg, Maria, Lidman, Olle, ... MHC2TA is associated with differential MHC molecule expression and susceptibility to rheumatoid arthritis, multiple sclerosis and myocardial infarction
in: Nature genetics . - New York, NY : Nature America, ISSN 1546-1718, Vol. 37, No. 5 (2005), p. 486-494
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2005