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Results of search for 'au:"Bartz, U"'
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Authors
Bartels, I
Bartz, U
Bartz, U G
Bayer, H
Bienzle, U
Bink, K
Bohlander, Stefan K
Claussen, U
Engel, W
Ernst, G
Forst, T
Gläser, B
Grün, G
Hartmann, R W
Hofferbert, S
Hoppe, C
Houge, G
Kehrer-Sawatzki, H
Kotzot, D
Krefft, M
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Topics
Adrenal Glands
Adult
Animals
Aromatase Inhibitors
Cattle
Female
Genetic Markers
Humans
In Situ Hybridization, Fluorescence
Karyotyping
Male
Mammary Neoplasms, Experimental
Mutation
Placenta
Polymerase Chain Reaction
Pregnancy
Rats
diagnosis
drug effects
genetics
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English
Your search returned 7 results.
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1.
Evaluation of the racemate and the enantiomers of a new highly active and selective aromatase inhibitor of the aminoglutethimide type.
[electronic resource]
by
Hartmann, R W
Grün, G
Bartz, U
Palzer, M
Producer:
19930203
In:
The Journal of steroid biochemistry and molecular biology
vol. 43
Online resources:
Available from publisher's website
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No items available.
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2.
Paternal origin of trisomy 21 following intracytoplasmic sperm injection (ICSI).
[electronic resource]
by
Bartels, I
Schlösser, M
Bartz, U G
Pauer, H U
Producer:
19990512
In:
Human reproduction (Oxford, England)
vol. 13
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3.
The novel acceptor splice site mutation 11396(G-->A) in the factor XII gene causes a truncated transcript in cross-reacting material negative patients.
[electronic resource]
by
Schloesser, M
Hofferbert, S
Bartz, U
Lutze, G
Lämmle, B
Engel, W
Producer:
19960126
In:
Human molecular genetics
vol. 4
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4.
Pyridyl-substituted tetrahydrocyclopropa[a]naphthalenes: highly active and selective inhibitors of P450 arom.
[electronic resource]
by
Hartmann, R W
Bayer, H
Grün, G
Sergejew, T
Bartz, U
Mitrenga, M
Producer:
19950714
In:
Journal of medicinal chemistry
vol. 38
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5.
Molecular cytogenetic analysis of a de novo balanced X;autosome translocation: Evidence for predominant inactivation of the derivative X chromosome in a girl with multiple malformations.
[electronic resource]
by
Gläser, B
Shirneshan, K
Bink, K
Wirth, J
Kehrer-Sawatzki, H
Bartz, U
Zoll, B
Bohlander, Stefan K
Producer:
20040423
In:
American journal of medical genetics. Part A
vol. 126A
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6.
Maternal uniparental disomy 12 in a healthy girl with a 47,XX,+der(12)(:p11-->q11:)/46,XX karyotype.
[electronic resource]
by
Von Eggeling, F
Hoppe, C
Bartz, U
Starke, H
Houge, G
Claussen, U
Ernst, G
Kotzot, D
Liehr, T
Producer:
20020905
In:
Journal of medical genetics
vol. 39
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7.
A fast and reliable single-run method for genotyping of the human cytochrome P450 2C8 gene for different ethnic groups.
[electronic resource]
by
Weise, A
Lambertz, U
Thomé, N
Bartz, U
Krefft, M
Mockenhaupt, F
Bienzle, U
Schöndorf, T
Forst, T
Pfützner, A
Producer:
20070129
In:
Clinical laboratory
vol. 52
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