Results
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41.
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42.
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Wilms tumor locus on 11p13 defined by multiple CpG island-associated transcripts. [electronic resource] by
- Bonetta, L
- Kuehn, S E
- Huang, A
- Law, D J
- Kalikin, L M
- Koi, M
- Reeve, A E
- Brownstein, B H
- Yeger, H
- Williams, B R
Producer: 19901227
In:
Science (New York, N.Y.) vol. 250
Availability: No items available.
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43.
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Multiple tumor suppressor genes in multistep carcinogenesis. [electronic resource] by
- Feinberg, A P
- Johnson, L A
- Law, D J
- Kuehn, S E
- Steenman, M
- Williams, B R
- Thomas, G
- Boland, C R
- Rainier, S
- Koi, M
Producer: 19930805
In:
The Tohoku journal of experimental medicine vol. 168
Availability: No items available.
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44.
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Tissue, developmental, and tumor-specific expression of divergent transcripts in Wilms tumor. [electronic resource] by
- Huang, A
- Campbell, C E
- Bonetta, L
- McAndrews-Hill, M S
- Chilton-MacNeill, S
- Coppes, M J
- Law, D J
- Feinberg, A P
- Yeger, H
- Williams, B R
Producer: 19901227
In:
Science (New York, N.Y.) vol. 250
Availability: No items available.
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45.
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Localization of the human estrogen-responsive finger protein (EEP) gene (ZNF147) within a YAC contig containing the myeloperoxidase (MPO) gene. [electronic resource] by
- Law, D J
- Prasad, M A
- King, S E
- Spranger, K D
- Lee, Y H
- Fox, R E
- Collins, E E
- Gebuhr, T C
- Miller, D E
- Petty, E M
Producer: 19960201
In:
Genomics vol. 28
Availability: No items available.
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46.
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A third Wilms' tumor locus on chromosome 16q. [electronic resource] by
- Maw, M A
- Grundy, P E
- Millow, L J
- Eccles, M R
- Dunn, R S
- Smith, P J
- Feinberg, A P
- Law, D J
- Paterson, M C
- Telzerow, P E
Producer: 19920630
In:
Cancer research vol. 52
Availability: No items available.
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47.
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Mutations in human TBX3 alter limb, apocrine and genital development in ulnar-mammary syndrome. [electronic resource] by
- Bamshad, M
- Lin, R C
- Law, D J
- Watkins, W C
- Krakowiak, P A
- Moore, M E
- Franceschini, P
- Lala, R
- Holmes, L B
- Gebuhr, T C
- Bruneau, B G
- Schinzel, A
- Seidman, J G
- Seidman, C E
- Jorde, L B
Producer: 19970729
In:
Nature genetics vol. 16
Availability: No items available.
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48.
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Holt-Oram syndrome is caused by mutations in TBX5, a member of the Brachyury (T) gene family. [electronic resource] by
- Li, Q Y
- Newbury-Ecob, R A
- Terrett, J A
- Wilson, D I
- Curtis, A R
- Yi, C H
- Gebuhr, T
- Bullen, P J
- Robson, S C
- Strachan, T
- Bonnet, D
- Lyonnet, S
- Young, I D
- Raeburn, J A
- Buckler, A J
- Law, D J
- Brook, J D
Producer: 19970128
In:
Nature genetics vol. 15
Availability: No items available.
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49.
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Multiple genetic loci within 11p15 defined by Beckwith-Wiedemann syndrome rearrangement breakpoints and subchromosomal transferable fragments. [electronic resource] by
- Hoovers, J M
- Kalikin, L M
- Johnson, L A
- Alders, M
- Redeker, B
- Law, D J
- Bliek, J
- Steenman, M
- Benedict, M
- Wiegant, J
- Lengauer, C
- Taillon-Miller, P
- Schlessinger, D
- Edwards, M C
- Elledge, S J
- Ivens, A
- Westerveld, A
- Little, P
- Mannens, M
- Feinberg, A P
Producer: 19960607
In:
Proceedings of the National Academy of Sciences of the United States of America vol. 92
Availability: No items available.
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