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Results of search for 'au:"Cervenková, M"'
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Authors
Aerts, J M
Befekadu, A
Berná, L
Böör, A
Cervenková, M
Elleder, M
Harzer, K
Hodanová, K
Hrebícek, M
Hulková, H
Ledvinová, J
Miloschewsky, D
Mrázová, L
Paton, B C
Poupetová, H
Smíd, F
Tochácková, M
Vepreková, L
Zeman, J
Zemen, J
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Anesthesia, Intravenous
Antigens, CD
Base Sequence
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DNA Mutational Analysis
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Gaucher Disease
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deficiency
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Your search returned 4 results.
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1.
Cardiovascular collapse following induction with propanidid.
[electronic resource]
by
Miloschewsky, D
Cervenková, M
Producer:
19701213
In:
British journal of anaesthesia
vol. 42
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2.
Incorrect assignment of N370S mutation status by mismatched PCR/RFLP method in two Gaucher patients.
[electronic resource]
by
Hodanová, K
Hrebícek, M
Cervenková, M
Aerts, J M
Zeman, J
Producer:
19971014
In:
Journal of inherited metabolic disease
vol. 20
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No items available.
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3.
Analysis of the beta-glucocerebrosidase gene in Czech and Slovak Gaucher patients: mutation profile and description of six novel mutant alleles.
[electronic resource]
by
Hodanová, K
Hrebícek, M
Cervenková, M
Mrázová, L
Vepreková, L
Zemen, J
Producer:
20000328
In:
Blood cells, molecules & diseases
vol. 25
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No items available.
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4.
A novel mutation in the coding region of the prosaposin gene leads to a complete deficiency of prosaposin and saposins, and is associated with a complex sphingolipidosis dominated by lactosylceramide accumulation.
[electronic resource]
by
Hulková, H
Cervenková, M
Ledvinová, J
Tochácková, M
Hrebícek, M
Poupetová, H
Befekadu, A
Berná, L
Paton, B C
Harzer, K
Böör, A
Smíd, F
Elleder, M
Producer:
20010802
In:
Human molecular genetics
vol. 10
Online resources:
Available from publisher's website
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No items available.
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