Results
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25641.
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25642.
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25643.
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25644.
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Genetic aberrations in glioblastoma multiforme: translocation of chromosome 10 in an O-2A-like cell line. [electronic resource] by
- Mao, X
- Jones, T A
- Tomlinson, I
- Rowan, A J
- Fedorova, L I
- Zelenin, A V
- Mao, J I
- Gutowski, N J
- Noble, M
- Sheer, D
Producer: 19990325
In:
British journal of cancer vol. 79
Availability: No items available.
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25645.
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Characterization of a germline mosaicism in families with Lowe syndrome, and identification of seven novel mutations in the OCRL1 gene. [electronic resource] by
- Satre, V
- Monnier, N
- Berthoin, F
- Ayuso, C
- Joannard, A
- Jouk, P S
- Lopez-Pajares, I
- Megabarne, A
- Philippe, H J
- Plauchu, H
- Torres, M L
- Lunardi, J
Producer: 19990805
In:
American journal of human genetics vol. 65
Availability: No items available.
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25646.
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25647.
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25648.
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25649.
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25650.
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Splicing mutations in KCNQ1: a mutation hot spot at codon 344 that produces in frame transcripts. [electronic resource] by
- Murray, A
- Donger, C
- Fenske, C
- Spillman, I
- Richard, P
- Dong, Y B
- Neyroud, N
- Chevalier, P
- Denjoy, I
- Carter, N
- Syrris, P
- Afzal, A R
- Patton, M A
- Guicheney, P
- Jeffery, S
Producer: 20000113
In:
Circulation vol. 100
Availability: No items available.
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25651.
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25652.
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Loss of heterozygosity at 3p23 is correlated with poor survival in patients with colorectal carcinoma. [electronic resource] by
- Iniesta, P
- Massa, M J
- González-Quevedo, R
- de Juan, C
- Morán, A
- Sánchez-Pernaute, A
- Cerdán, J
- Torres, A
- Balibrea, J L
- Benito, M
Producer: 20001003
In:
Cancer vol. 89
Availability: No items available.
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25653.
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25654.
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Strong Amerind/white sex bias and a possible Sephardic contribution among the founders of a population in northwest Colombia. [electronic resource] by
- Carvajal-Carmona, L G
- Soto, I D
- Pineda, N
- Ortíz-Barrientos, D
- Duque, C
- Ospina-Duque, J
- McCarthy, M
- Montoya, P
- Alvarez, V M
- Bedoya, G
- Ruiz-Linares, A
Producer: 20001214
In:
American journal of human genetics vol. 67
Availability: No items available.
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25655.
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25656.
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25657.
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25658.
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25659.
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25660.
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Dominant modifier DFNM1 suppresses recessive deafness DFNB26. [electronic resource] by
- Riazuddin, S
- Castelein, C M
- Ahmed, Z M
- Lalwani, A K
- Mastroianni, M A
- Naz, S
- Smith, T N
- Liburd, N A
- Friedman, T B
- Griffith, A J
- Riazuddin, S
- Wilcox, E R
Producer: 20010104
In:
Nature genetics vol. 26
Availability: No items available.
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