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161.
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Integration of transcript and genetic maps of chromosome 16 at near-1-Mb resolution: demonstration of a "hot spot" for recombination at 16p12. [electronic resource] by
- Callen, D F
- Lane, S A
- Kozman, H
- Kremmidiotis, G
- Whitmore, S A
- Lowenstein, M
- Doggett, N A
- Kenmochi, N
- Page, D C
- Maglott, D R
Producer: 19960807
In:
Genomics vol. 29
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162.
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163.
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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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164.
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Structure and chromosomal localization of the human renal kallikrein gene. [electronic resource] by
- Evans, B A
- Yun, Z X
- Close, J A
- Tregear, G W
- Kitamura, N
- Nakanishi, S
- Callen, D F
- Baker, E
- Hyland, V J
- Sutherland, G R
Producer: 19880819
In:
Biochemistry vol. 27
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165.
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Interleukin 4 is at 5q31 and interleukin 6 is at 7p15. [electronic resource] by
- Sutherland, G R
- Baker, E
- Callen, D F
- Hyland, V J
- Wong, G
- Clark, S
- Jones, S S
- Eglinton, L K
- Shannon, M F
- Lopez, A F
Producer: 19880928
In:
Human genetics vol. 79
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166.
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Isolation and use of chromosome 1 probes for linkage studies on Charcot-Marie-Tooth disease. [electronic resource] by
- Griffiths, L R
- Zwi, M B
- Mesterovic, N
- Ross, D A
- Board, P G
- Callen, D F
- Mohandas, T
- Buckland, R
- Fletcher, J M
- Driesel, A J
Producer: 19900507
In:
Annals of human genetics vol. 54
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167.
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Physical mapping of new DNA probes near the fragile X mutation (FRAXA) by using a panel of cell lines. [electronic resource] by
- Suthers, G K
- Hyland, V J
- Callen, D F
- Oberle, I
- Rocchi, M
- Thomas, N S
- Morris, C P
- Schwartz, C E
- Schmidt, M
- Ropers, H H
Producer: 19900904
In:
American journal of human genetics vol. 47
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168.
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Mapping of two phenol sulphotransferase genes, STP and STM, to 16p: candidate genes for Batten disease. [electronic resource] by
- Dooley, T P
- Mitchison, H M
- Munroe, P B
- Probst, P
- Neal, M
- Siciliano, M J
- Deng, Z
- Doggett, N A
- Callen, D F
- Gardiner, R M
Producer: 19950117
In:
Biochemical and biophysical research communications vol. 205
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169.
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A novel gene encoding an integral membrane protein is mutated in nephropathic cystinosis. [electronic resource] by
- Town, M
- Jean, G
- Cherqui, S
- Attard, M
- Forestier, L
- Whitmore, S A
- Callen, D F
- Gribouval, O
- Broyer, M
- Bates, G P
- van't Hoff, W
- Antignac, C
Producer: 19980423
In:
Nature genetics vol. 18
Availability: No items available.
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170.
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Frequent deletions at Xq28 indicate genetic heterogeneity in Hunter syndrome. [electronic resource] by
- Wilson, P J
- Suthers, G K
- Callen, D F
- Baker, E
- Nelson, P V
- Cooper, A
- Wraith, J E
- Sutherland, G R
- Morris, C P
- Hopwood, J J
Producer: 19910520
In:
Human genetics vol. 86
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171.
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High-resolution cytogenetic-based physical map of human chromosome 16. [electronic resource] by
- Callen, D F
- Doggett, N A
- Stallings, R L
- Chen, L Z
- Whitmore, S A
- Lane, S A
- Nancarrow, J K
- Apostolou, S
- Thompson, A D
- Lapsys, N M
Producer: 19920922
In:
Genomics vol. 13
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172.
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Fine genetic mapping of the Batten disease locus (CLN3) by haplotype analysis and demonstration of allelic association with chromosome 16p microsatellite loci. [electronic resource] by
- Mitchison, H M
- Thompson, A D
- Mulley, J C
- Kozman, H M
- Richards, R I
- Callen, D F
- Stallings, R L
- Doggett, N A
- Attwood, J
- McKay, T R
Producer: 19930726
In:
Genomics vol. 16
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173.
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A new DNA marker tightly linked to the fragile X locus (FRAXA). [electronic resource] by
- Suthers, G K
- Callen, D F
- Hyland, V J
- Kozman, H M
- Baker, E
- Eyre, H
- Harper, P S
- Roberts, S H
- Hors-Cayla, M C
- Davies, K E
Producer: 19900111
In:
Science (New York, N.Y.) vol. 246
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174.
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Refined genetic mapping of juvenile-onset neuronal ceroid-lipofuscinosis on chromosome 16. [electronic resource] by
- Mitchison, H M
- Williams, R E
- McKay, T R
- Callen, D F
- Thompson, A D
- Mulley, J C
- Stallings, R L
- Hildebrand, C E
- Moyzis, R K
- Järvelä, I
Producer: 19931025
In:
Journal of inherited metabolic disease vol. 16
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175.
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Analysis of lymphoedema-distichiasis families for FOXC2 mutations reveals small insertions and deletions throughout the gene. [electronic resource] by
- Bell, R
- Brice, G
- Child, A H
- Murday, V A
- Mansour, S
- Sandy, C J
- Collin, J R
- Brady, A F
- Callen, D F
- Burnand, K
- Mortimer, P
- Jeffery, S
Producer: 20010823
In:
Human genetics vol. 108
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176.
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YAC and cosmid contigs spanning the Batten disease (CLN3) region at 16p12.1-p11.2. [electronic resource] by
- Järvelä, I E
- Mitchison, H M
- O'Rawe, A M
- Munroe, P B
- Taschner, P E
- de Vos, N
- Lerner, T J
- D'Arigo, K L
- Callen, D F
- Thompson, A D
Producer: 19960807
In:
Genomics vol. 29
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177.
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A novel Q378X mutation exists in the transmembrane transporter protein ABCC6 and its pseudogene: implications for mutation analysis in pseudoxanthoma elasticum. [electronic resource] by
- Cai, L
- Lumsden, A
- Guenther, U P
- Neldner, S A
- Zäch, S
- Knoblauch, H
- Ramesar, R
- Hohl, D
- Callen, D F
- Neldner, K H
- Lindpaintner, K
- Richards, R I
- Struk, B
Producer: 20020114
In:
Journal of molecular medicine (Berlin, Germany) vol. 79
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178.
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Mutant p53 drives invasion in breast tumors through up-regulation of miR-155. [electronic resource] by
- Neilsen, P M
- Noll, J E
- Mattiske, S
- Bracken, C P
- Gregory, P A
- Schulz, R B
- Lim, S P
- Kumar, R
- Suetani, R J
- Goodall, G J
- Callen, D F
Producer: 20130814
In:
Oncogene vol. 32
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179.
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Analysis of Australian Crohn's disease pedigrees refines the localization for susceptibility to inflammatory bowel disease on chromosome 16. [electronic resource] by
- Cavanaugh, J A
- Callen, D F
- Wilson, S R
- Stanford, P M
- Sraml, M E
- Gorska, M
- Crawford, J
- Whitmore, S A
- Shlegel, C
- Foote, S
- Kohonen-Corish, M
- Pavli, P
Producer: 19990413
In:
Annals of human genetics vol. 62
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180.
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Mutation analysis of the Fanconi anaemia A gene in breast tumours with loss of heterozygosity at 16q24.3. [electronic resource] by
- Cleton-Jansen, A M
- Moerland, E W
- Pronk, J C
- van Berkel, C G
- Apostolou, S
- Crawford, J
- Savoia, A
- Auerbach, A D
- Mathew, C G
- Callen, D F
- Cornelisse, C J
Producer: 19990413
In:
British journal of cancer vol. 79
Availability: No items available.
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