Results
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Further localization of the gene for hereditary paragangliomas and evidence for linkage in unrelated families. [electronic resource] by
- Heutink, P
- van Schothorst, E M
- van der Mey, A G
- Bardoel, A
- Breedveld, G
- Pertijs, J
- Sandkuijl, L A
- van Ommen, G J
- Cornelisse, C J
- Oostra, B A
Producer: 19950227
In:
European journal of human genetics : EJHG vol. 2
Availability: No items available.
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31.
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Confinement of PGL, an imprinted gene causing hereditary paragangliomas, to a 2-cM interval on 11q22-q23 and exclusion of DRD2 and NCAM as candidate genes. [electronic resource] by
- van Schothorst, E M
- Jansen, J C
- Bardoel, A F
- van der Mey, A G
- James, M J
- Sobol, H
- Weissenbach, J
- van Ommen, G J
- Cornelisse, C J
- Devilee, P
Producer: 19970304
In:
European journal of human genetics : EJHG vol. 4
Availability: No items available.
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32.
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33.
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Nearly all hereditary paragangliomas in the Netherlands are caused by two founder mutations in the SDHD gene. [electronic resource] by
- Taschner, P E
- Jansen, J C
- Baysal, B E
- Bosch, A
- Rosenberg, E H
- Bröcker-Vriends, A H
- van Der Mey, A G
- van Ommen, G J
- Cornelisse, C J
- Devilee, P
Producer: 20010705
In:
Genes, chromosomes & cancer vol. 31
Availability: No items available.
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34.
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A gene subject to genomic imprinting and responsible for hereditary paragangliomas maps to chromosome 11q23-qter. [electronic resource] by
- Heutink, P
- van der Mey, A G
- Sandkuijl, L A
- van Gils, A P
- Bardoel, A
- Breedveld, G J
- van Vliet, M
- van Ommen, G J
- Cornelisse, C J
- Oostra, B A
Producer: 19930528
In:
Human molecular genetics vol. 1
Availability: No items available.
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35.
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36.
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37.
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Paragangliomas of the head and neck region show complete loss of heterozygosity at 11q22-q23 in chief cells and the flow-sorted DNA aneuploid fraction. [electronic resource] by
- van Schothorst, E M
- Beekman, M
- Torremans, P
- Kuipers-Dijkshoorn, N J
- Wessels, H W
- Bardoel, A F
- van der Mey, A G
- van der Vijver, M J
- van Ommen, G J
- Devilee, P
- Cornelisse, C J
Producer: 19981105
In:
Human pathology vol. 29
Availability: No items available.
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38.
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Mutations in SDHD are the major determinants of the clinical characteristics of Dutch head and neck paraganglioma patients. [electronic resource] by
- Hensen, E F
- Siemers, M D
- Jansen, J C
- Corssmit, E P M
- Romijn, J A
- Tops, C M J
- van der Mey, A G L
- Devilee, P
- Cornelisse, C J
- Bayley, J P
- Vriends, A H J T
Producer: 20120510
In:
Clinical endocrinology vol. 75
Availability: No items available.
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39.
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High prevalence of founder mutations of the succinate dehydrogenase genes in the Netherlands. [electronic resource] by
- Hensen, E F
- van Duinen, N
- Jansen, J C
- Corssmit, E P M
- Tops, C M J
- Romijn, J A
- Vriends, A H J T
- van der Mey, A G L
- Cornelisse, C J
- Devilee, P
- Bayley, J P
Producer: 20120808
In:
Clinical genetics vol. 81
Availability: No items available.
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40.
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Increased prevalence of catecholamine excess and phaeochromocytomas in a well-defined Dutch population with SDHD-linked head and neck paragangliomas. [electronic resource] by
- van Houtum, W H
- Corssmit, E P M
- Douwes Dekker, P B
- Jansen, J C
- van der Mey, A G L
- Bröcker-Vriends, A H J T
- Taschner, P E M
- Losekoot, M
- Frölich, M
- Stokkel, M P M
- Cornelisse, C J
- Romijn, J A
Producer: 20050331
In:
European journal of endocrinology vol. 152
Availability: No items available.
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