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Results of search for 'au:"Christensen, Signe E"'
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Authors
Brixen, Kim
Christensen, Signe E
Heickendorff, Lene
Ladefoged, Søren A
Mosekilde, Leif
Nissen, Peter H
Vestergaard, Peter
Wallace, Andrew
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Topics
Calcium
Calcium Metabolism Disorders
Codon
Computational Biology
Creatinine
DNA
DNA Copy Number Variations
DNA Mutational Analysis
Denmark
Exons
Gene Frequency
Genetic Testing
Genetic Variation
Humans
Hypercalcemia
Hypocalcemia
Mutation
Receptors, Calcium-Sensing
blood
genetics
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English
Your search returned 4 results.
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1.
Familial hypocalciuric hypercalcaemia: a review.
[electronic resource]
by
Christensen, Signe E
Nissen, Peter H
Vestergaard, Peter
Mosekilde, Leif
Producer:
20120605
In:
Current opinion in endocrinology, diabetes, and obesity
vol. 18
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Available from publisher's website
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2.
Molecular genetic analysis of the calcium sensing receptor gene in patients clinically suspected to have familial hypocalciuric hypercalcemia: phenotypic variation and mutation spectrum in a Danish population.
[electronic resource]
by
Nissen, Peter H
Christensen, Signe E
Heickendorff, Lene
Brixen, Kim
Mosekilde, Leif
Producer:
20080102
In:
The Journal of clinical endocrinology and metabolism
vol. 92
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3.
Multiplex ligation-dependent probe amplification (MLPA) screening for exon copy number variation in the calcium sensing receptor gene: no large rearrangements identified in patients with calcium metabolic disorders.
[electronic resource]
by
Nissen, Peter H
Christensen, Signe E
Wallace, Andrew
Heickendorff, Lene
Brixen, Kim
Mosekilde, Leif
Producer:
20100928
In:
Clinical endocrinology
vol. 72
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4.
Identification of rare and frequent variants of the CASR gene by high-resolution melting.
[electronic resource]
by
Nissen, Peter H
Christensen, Signe E
Ladefoged, Søren A
Brixen, Kim
Heickendorff, Lene
Mosekilde, Leif
Producer:
20120517
In:
Clinica chimica acta; international journal of clinical chemistry
vol. 413
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