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S. M. Klauck

Veröffentlichungen von S. M. Klauck zu Klauck, S. M. ->
weitere Veröffentlichungen von S. M. Klauck:
The Hemofiltrate of Human Patients: A Favourable Source of Endogenous Digitalis-Like Substances (1993)
HSV type 1 genome variants from persistently productive infections in Raji and BJAB cell lines (1995)
Evolutionary conservation and genomic organization of XAP-4, an Xq28 located gene coding for a human rab GDP-dissociation inhibitor (GDI) (1994)
Molecular genetic analysis of the FMR-1 gene in a large collection of autistic patients (1997)
X-linked dyskeratosis congenita is caused by mutations in a highly conserved gene with putative nucleolar functions (1998)
The 5-HT transporter gene-linked polymorphic region (5-HTTLPR) in evolutionary perspective: Alternative biallelic variation in rhesus monkeys (1997)
Molecular cytogenetics in von Hippel-Lindau disease (1993)
Cytogenetic and fluorescence in situ hybridization studies on sporadic and hereditary tumors associated with von Hippel-Lindau syndrome (VHL) (1994)
Cytogenetic and molecular studies of a familial renal cell carcinoma (1992)
Automatic reduction of NMR spectroscopic data for statistical and pattern recognition classification of samples (1994)
Genomic rearrangement in NEMO impairs NF-κB activation andis a cause of incontinentia pigmenti (2000)
Mapping autism risk loci using genetic linkage and chromosomal rearrangements (2007)
Abstract (1992)
Veröffentlichungen zu Klauck, S. M.
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1
Walter, U.. The Hemofiltrate of Human Patients: A Favourable Source of Endogenous Digitalis-Like Substances
In: Planta medica. - Stuttgart [u.a.] : Thieme Vol. 59, No. S 1 (12. 1993), p. 639-639
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1993
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2
Klauck, S. M., Hampl, W., ... HSV type 1 genome variants from persistently productive infections in Raji and BJAB cell lines
in: Archives of virology , ISSN 1432-8798, Vol. 140 (7. 1995), p. 1195-1213
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1995
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3
Sedlacek, Z., Konecki, D. S., ... Evolutionary conservation and genomic organization of XAP-4, an Xq28 located gene coding for a human rab GDP-dissociation inhibitor (GDI)
in: Mammalian genome , ISSN 1432-1777, Vol. 5 (10. 1994), p. 633-639
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1994
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4
Klauck, S. M., Münstermann, Ewald, ... Molecular genetic analysis of the FMR-1 gene in a large collection of autistic patients
in: Human genetics , ISSN 1432-1203, Vol. 100 (2. 1997), p. 224-229
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1997
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5
Heiss, Nina S., Knight, Stuart W., ... X-linked dyskeratosis congenita is caused by mutations in a highly conserved gene with putative nucleolar functions
in: Nature genetics . - New York, NY : Nature America, ISSN 1546-1718, Vol. 19, No. 1 (1998), p. 32-38
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1998
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6
Lesch, K. P., Meyer, J., ... The 5-HT transporter gene-linked polymorphic region (5-HTTLPR) in evolutionary perspective: Alternative biallelic variation in rhesus monkeys
in: Journal of neural transmission , ISSN 1435-1463, Vol. 104 (11/12. 1997), p. 1259-1266
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1997
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7
Decker, H.J., McNeil, J., ... Molecular cytogenetics in von Hippel-Lindau disease
in: Cancer Genetics and Cytogenetics, in: Cancer Genetics and Cytogenetics . - Amsterdam : Elsevier, ISSN 0165-4608, ZDB-ID 2004205-X Vol. 66, No. 2 (1993), p. 163
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1993
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8
Decker, H.-J.H., Klauck, S.M., ... Cytogenetic and fluorescence in situ hybridization studies on sporadic and hereditary tumors associated with von Hippel-Lindau syndrome (VHL)
in: Cancer Genetics and Cytogenetics, in: Cancer Genetics and Cytogenetics . - Amsterdam : Elsevier, ISSN 0165-4608, ZDB-ID 2004205-X Vol. 77, No. 1 (1994), p. 1-13
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1994
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9
Decker, H.-J.H., Wullich, B., ... Cytogenetic and molecular studies of a familial renal cell carcinoma
in: Cancer Genetics and Cytogenetics, in: Cancer Genetics and Cytogenetics . - Amsterdam : Elsevier, ISSN 0165-4608, ZDB-ID 2004205-X Vol. 63, No. 1 (1992), p. 25-31
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1992
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10
Spraul, M., Neidig, P., ... Automatic reduction of NMR spectroscopic data for statistical and pattern recognition classification of samples
in: Journal of Pharmaceutical and Biomedical Analysis, in: Journal of Pharmaceutical and Biomedical Analysis . - Amsterdam : Elsevier, ISSN 0731-7085, ZDB-ID 1491820-1 Vol. 12, No. 10 (1994), p. 1215-1225
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1994
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11
Smahi, Asmae, Courtois, G., ... Genomic rearrangement in NEMO impairs NF-κB activation andis a cause of incontinentia pigmenti
in: Nature . - London [u.a.] : Nature Publising Group, ISSN 1476-4687, Vol. 405, No. 6785 (2000), p. 466-472
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2000
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12
Szatmari, Peter, Paterson, Andrew D, ... Mapping autism risk loci using genetic linkage and chromosomal rearrangements
in: Nature genetics . - New York, NY : Nature America, ISSN 1546-1718, Vol. 39, No. 3 (2007), p. 319-328
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2007
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13
Mache, Ch., Urban, Ch., ... Abstract
in: Annals of hematology , ISSN 1432-0584, Vol. 65 (1. 1992), p. A1
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1992