Results
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141.
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142.
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Probe, VK5B, is located in the same interval as the autosomal dominant adult polycystic kidney disease locus, PKD1. [electronic resource] by
- Hyland, V J
- Suthers, G K
- Friend, K
- MacKinnon, R N
- Callen, D F
- Breuning, M H
- Keith, T
- Brown, V A
- Phipps, P
- Sutherland, G R
Producer: 19900322
In:
Human genetics vol. 84
Availability: No items available.
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143.
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Adult, fetal, and polycystic kidney expression of polycystin, the polycystic kidney disease-1 gene product. [electronic resource] by
- Peters, D J
- Spruit, L
- Klingel, R
- Prins, F
- Baelde, H J
- Giordano, P C
- Bernini, L F
- de Heer, E
- Breuning, M H
- Bruijn, J A
Producer: 19961001
In:
Laboratory investigation; a journal of technical methods and pathology vol. 75
Availability: No items available.
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144.
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145.
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146.
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Improved interpretation of complex chromosomal rearrangements by combined GTG banding and in situ suppression hybridization using chromosome-specific libraries and cosmid probes. [electronic resource] by
- Smit, V T
- Wessels, J W
- Mollevanger, P
- Dauwerse, J G
- van Vliet, M
- Beverstock, G C
- Breuning, M H
- Devilee, P
- Raap, A K
- Cornelisse, C J
Producer: 19920106
In:
Genes, chromosomes & cancer vol. 3
Availability: No items available.
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147.
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Recurrent digital fibroma, focal dermal hypoplasia, and limb malformations. [electronic resource] by
- Breuning, M H
- Oranje, A P
- Langemeijer, R A
- Hovius, S E
- Diepstraten, A F
- den Hollander, J C
- Baumgartner, N
- Dwek, J R
- Sommer, A
- Toriello, H
Producer: 20001019
In:
American journal of medical genetics vol. 94
Availability: No items available.
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148.
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Batten disease gene, CLN3: linkage disequilibrium mapping in the Finnish population, and analysis of European haplotypes. [electronic resource] by
- Mitchison, H M
- O'Rawe, A M
- Taschner, P E
- Sandkuijl, L A
- Santavuori, P
- de Vos, N
- Breuning, M H
- Mole, S E
- Gardiner, R M
- Järvelä, I E
Producer: 19950413
In:
American journal of human genetics vol. 56
Availability: No items available.
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149.
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150.
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A large duplicated area in the polycystic kidney disease 1 (PKD1) region of chromosome 16 is prone to rearrangement. [electronic resource] by
- Harris, P C
- Thomas, S
- MacCarthy, A B
- Stallings, R L
- Breuning, M H
- Jenne, D E
- Fink, T M
- Buckle, V J
- Ratcliffe, P J
- Ward, C J
Producer: 19950224
In:
Genomics vol. 23
Availability: No items available.
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151.
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Mechanisms of MRP over-expression in four human lung-cancer cell lines and analysis of the MRP amplicon. [electronic resource] by
- Eijdems, E W
- De Haas, M
- Coco-Martin, J M
- Ottenheim, C P
- Zaman, G J
- Dauwerse, H G
- Breuning, M H
- Twentyman, P R
- Borst, P
- Baas, F
Producer: 19950323
In:
International journal of cancer vol. 60
Availability: No items available.
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152.
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Rapid detection of chromosome 16 inversion in acute nonlymphocytic leukemia, subtype M4: regional localization of the breakpoint in 16p. [electronic resource] by
- Dauwerse, J G
- Kievits, T
- Beverstock, G C
- van der Keur, D
- Smit, E
- Wessels, H W
- Hagemeijer, A
- Pearson, P L
- van Ommen, G J
- Breuning, M H
Producer: 19900821
In:
Cytogenetics and cell genetics vol. 53
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153.
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154.
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A murine model for juvenile NCL: gene targeting of mouse Cln3. [electronic resource] by
- Greene, N D
- Bernard, D L
- Taschner, P E
- Lake, B D
- de Vos, N
- Breuning, M H
- Gardiner, R M
- Mole, S E
- Nussbaum, R L
- Mitchison, H M
Producer: 19990622
In:
Molecular genetics and metabolism vol. 66
Availability: No items available.
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155.
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Carrier detection of Batten disease (juvenile neuronal ceroid-lipofuscinosis). [electronic resource] by
- Taschner, P E
- de Vos, N
- Post, J G
- Meijers-Heijboer, E J
- Hofman, I
- Loonen, M C
- Pinckers, A J
- Bleeker-Wagemakers, E M
- Gardiner, R M
- Breuning, M H
Producer: 19951011
In:
American journal of medical genetics vol. 57
Availability: No items available.
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156.
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Individuals with abnormal phenotype and normal G-banding karyotype: improvement and limitations in the diagnosis by the use of 24-colour FISH. [electronic resource] by
- Bezrookove, V
- Hansson, K
- van der Burg, M
- van der Smagt, J J
- Hilhorst-Hofstee, Y
- Wiegant, J
- Beverstock, G C
- Raap, A K
- Tanke, H
- Breuning, M H
- Rosenberg, C
Producer: 20000614
In:
Human genetics vol. 106
Availability: No items available.
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157.
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Germline mutations in APC and MUTYH are responsible for the majority of families with attenuated familial adenomatous polyposis. [electronic resource] by
- Nielsen, M
- Hes, F J
- Nagengast, F M
- Weiss, M M
- Mathus-Vliegen, E M
- Morreau, H
- Breuning, M H
- Wijnen, J T
- Tops, C M J
- Vasen, H F A
Producer: 20070725
In:
Clinical genetics vol. 71
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158.
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159.
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Duplications in the DMD gene. [electronic resource] by
- White, S J
- Aartsma-Rus, A
- Flanigan, K M
- Weiss, R B
- Kneppers, A L J
- Lalic, T
- Janson, A A M
- Ginjaar, H B
- Breuning, M H
- den Dunnen, J T
Producer: 20061024
In:
Human mutation vol. 27
Availability: No items available.
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160.
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Genomic imbalances in mental retardation. [electronic resource] by
- Kriek, M
- White, S J
- Bouma, M C
- Dauwerse, H G
- Hansson, K B M
- Nijhuis, J V
- Bakker, B
- van Ommen, G-J B
- den Dunnen, J T
- Breuning, M H
Producer: 20040507
In:
Journal of medical genetics vol. 41
Availability: No items available.
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