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Informatic selection of a neural crest-melanocyte cDNA set for microarray analysis. [electronic resource] by
- Loftus, S K
- Chen, Y
- Gooden, G
- Ryan, J F
- Birznieks, G
- Hilliard, M
- Baxevanis, A D
- Bittner, M
- Meltzer, P
- Trent, J
- Pavan, W
Producer: 19990909
In:
Proceedings of the National Academy of Sciences of the United States of America vol. 96
Availability: No items available.
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50.
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Pendred syndrome is caused by mutations in a putative sulphate transporter gene (PDS). [electronic resource] by
- Everett, L A
- Glaser, B
- Beck, J C
- Idol, J R
- Buchs, A
- Heyman, M
- Adawi, F
- Hazani, E
- Nassir, E
- Baxevanis, A D
- Sheffield, V C
- Green, E D
Producer: 19971229
In:
Nature genetics vol. 17
Availability: No items available.
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52.
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Loss-of-function mutations in growth differentiation factor-1 (GDF1) are associated with congenital heart defects in humans. [electronic resource] by
- Karkera, J D
- Lee, J S
- Roessler, E
- Banerjee-Basu, S
- Ouspenskaia, M V
- Mez, J
- Goldmuntz, E
- Bowers, P
- Towbin, J
- Belmont, J W
- Baxevanis, A D
- Schier, A F
- Muenke, M
Producer: 20071127
In:
American journal of human genetics vol. 81
Availability: No items available.
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53.
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Progressive juvenile-onset punctate cataracts caused by mutation of the gammaD-crystallin gene. [electronic resource] by
- Stephan, D A
- Gillanders, E
- Vanderveen, D
- Freas-Lutz, D
- Wistow, G
- Baxevanis, A D
- Robbins, C M
- VanAuken, A
- Quesenberry, M I
- Bailey-Wilson, J
- Juo, S H
- Trent, J M
- Smith, L
- Brownstein, M J
Producer: 19990305
In:
Proceedings of the National Academy of Sciences of the United States of America vol. 96
Availability: No items available.
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54.
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The human RGL (RalGDS-like) gene: cloning, expression analysis and genomic organization. [electronic resource] by
- Sood, R
- Makalowska, I
- Carpten, J D
- Robbins, C M
- Stephan, D A
- Connors, T D
- Morgenbesser, S D
- Su, K
- Pinkett, H W
- Graham, C L
- Quesenberry, M I
- Baxevanis, A D
- Klinger, K W
- Trent, J M
- Bonner, T I
Producer: 20000706
In:
Biochimica et biophysica acta vol. 1491
Availability: No items available.
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55.
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Cloning and characterization of 13 novel transcripts and the human RGS8 gene from the 1q25 region encompassing the hereditary prostate cancer (HPC1) locus. [electronic resource] by
- Sood, R
- Bonner, T I
- Makalowska, I
- Stephan, D A
- Robbins, C M
- Connors, T D
- Morgenbesser, S D
- Su, K
- Faruque, M U
- Pinkett, H
- Graham, C
- Baxevanis, A D
- Klinger, K W
- Landes, G M
- Trent, J M
- Carpten, J D
Producer: 20010823
In:
Genomics vol. 73
Availability: No items available.
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56.
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A 6-Mb high-resolution physical and transcription map encompassing the hereditary prostate cancer 1 (HPC1) region. [electronic resource] by
- Carpten, J D
- Makalowska, I
- Robbins, C M
- Scott, N
- Sood, R
- Connors, T D
- Bonner, T I
- Smith, J R
- Faruque, M U
- Stephan, D A
- Pinkett, H
- Morgenbesser, S D
- Su, K
- Graham, C
- Gregory, S G
- Williams, H
- McDonald, L
- Baxevanis, A D
- Klingler, K W
- Landes, G M
- Trent, J M
Producer: 20000608
In:
Genomics vol. 64
Availability: No items available.
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