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Results of search for 'au:"Rötzer, E"'
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Authors
Berninger, T
Blankenagel, A
Burgemeister, R
Carvalho, M R
Gehrke, M
Goebel, H H
Gross, M
Gutensohn, W
Kommerell, G
Kölle, P
Lochmüller, H
Lorenz, B
Mahnke-Zizelman, D K
Meitinger, T
Mortier, W
Müller, B
Pongratz, D
Reichmann, H
Rötzer, E
Sabina, R L
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Topics
AMP Deaminase
Alleles
Amino Acid Sequence
Amino Acid Substitution
Anxiety
Base Sequence
Blotting, Western
Codon, Terminator
DNA
DNA Primers
DNA Probes
DNA, Complementary
Exons
Humans
Mutation
Polymerase Chain Reaction
blood
deficiency
enzymology
genetics
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English
German
Your search returned 6 results.
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1.
[Cases from practice with special consideration of the premedication before dental procedures].
[electronic resource]
by
Rötzer, E
Producer:
19700326
In:
Der Zahnarzt; Colloquium med. dent
vol. 13
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No items available.
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2.
Rapid DNA extraction method for genetic screening.
[electronic resource]
by
Gross, M
Rötzer, E
Producer:
19980423
In:
European journal of medical research
vol. 3
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3.
The genetic basis of myoadenylate deaminase deficiency is heterogeneous.
[electronic resource]
by
Rötzer, E
Mortier, W
Reichmann, H
Gross, M
Producer:
19980723
In:
Advances in experimental medicine and biology
vol. 431
Online resources:
Available from publisher's website
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4.
Identification of a new missense mutation in exon 2 of the human hypoxanthine phosphoribosyltransferase gene (HPRTIsar): a further example of clinical heterogeneity in HPRT deficiencies.
[electronic resource]
by
Burgemeister, R
Rötzer, E
Gutensohn, W
Gehrke, M
Schiel, W
Producer:
19950906
In:
Human mutation
vol. 5
Online resources:
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5.
Leber's hereditary optic neuroretinopathy and the X-chromosomal susceptibility factor: no linkage to DXs7.
[electronic resource]
by
Carvalho, M R
Müller, B
Rötzer, E
Berninger, T
Kommerell, G
Blankenagel, A
Savontaus, M L
Meitinger, T
Lorenz, B
Producer:
19930114
In:
Human heredity
vol. 42
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6.
A G468-T AMPD1 mutant allele contributes to the high incidence of myoadenylate deaminase deficiency in the Caucasian population.
[electronic resource]
by
Gross, M
Rötzer, E
Kölle, P
Mortier, W
Reichmann, H
Goebel, H H
Lochmüller, H
Pongratz, D
Mahnke-Zizelman, D K
Sabina, R L
Producer:
20021009
In:
Neuromuscular disorders : NMD
vol. 12
Online resources:
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