Results
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27001.
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27002.
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27003.
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A novel, heritable, expanding CTG repeat in an intron of the SEF2-1 gene on chromosome 18q21.1. [electronic resource] by
- Breschel, T S
- McInnis, M G
- Margolis, R L
- Sirugo, G
- Corneliussen, B
- Simpson, S G
- McMahon, F J
- MacKinnon, D F
- Xu, J F
- Pleasant, N
- Huo, Y
- Ashworth, R G
- Grundstrom, C
- Grundstrom, T
- Kidd, K K
- DePaulo, J R
- Ross, C A
Producer: 19980102
In:
Human molecular genetics vol. 6
Availability: No items available.
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27004.
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27005.
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27006.
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A novel phenotypic pattern in X-linked inheritance: craniofrontonasal syndrome maps to Xp22. [electronic resource] by
- Feldman, G J
- Ward, D E
- Lajeunie-Renier, E
- Saavedra, D
- Robin, N H
- Proud, V
- Robb, L J
- Der Kaloustian, V
- Carey, J C
- Cohen, M M
- Cormier, V
- Munnich, A
- Zackai, E H
- Wilkie, A O
- Price, R A
- Muenke, M
Producer: 19980102
In:
Human molecular genetics vol. 6
Availability: No items available.
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27007.
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Genetic modification of the phenotypes produced by amyloid precursor protein overexpression in transgenic mice. [electronic resource] by
- Carlson, G A
- Borchelt, D R
- Dake, A
- Turner, S
- Danielson, V
- Coffin, J D
- Eckman, C
- Meiners, J
- Nilsen, S P
- Younkin, S G
- Hsiao, K K
Producer: 19980102
In:
Human molecular genetics vol. 6
Availability: No items available.
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27008.
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27009.
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27010.
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27011.
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27012.
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27013.
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27014.
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27015.
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27016.
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27017.
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27018.
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27019.
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27020.
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