Results
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29461.
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WRN helicase is a synthetic lethal target in microsatellite unstable cancers. [electronic resource] by
- Chan, Edmond M
- Shibue, Tsukasa
- McFarland, James M
- Gaeta, Benjamin
- Ghandi, Mahmoud
- Dumont, Nancy
- Gonzalez, Alfredo
- McPartlan, Justine S
- Li, Tianxia
- Zhang, Yanxi
- Bin Liu, Jie
- Lazaro, Jean-Bernard
- Gu, Peili
- Piett, Cortt G
- Apffel, Annie
- Ali, Syed O
- Deasy, Rebecca
- Keskula, Paula
- Ng, Raymond W S
- Roberts, Emma A
- Reznichenko, Elizaveta
- Leung, Lisa
- Alimova, Maria
- Schenone, Monica
- Islam, Mirazul
- Maruvka, Yosef E
- Liu, Yang
- Roper, Jatin
- Raghavan, Srivatsan
- Giannakis, Marios
- Tseng, Yuen-Yi
- Nagel, Zachary D
- D'Andrea, Alan
- Root, David E
- Boehm, Jesse S
- Getz, Gad
- Chang, Sandy
- Golub, Todd R
- Tsherniak, Aviad
- Vazquez, Francisca
- Bass, Adam J
Producer: 20191216
In:
Nature vol. 568
Availability: No items available.
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29462.
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Prenatal diagnosis of uniparental disomy 15 following trisomy 15 mosaicism. [electronic resource] by
- Christian, S L
- Smith, A C
- Macha, M
- Black, S H
- Elder, F F
- Johnson, J M
- Resta, R G
- Surti, U
- Suslak, L
- Verp, M S
- Ledbetter, D H
Producer: 19961022
In:
Prenatal diagnosis vol. 16
Availability: No items available.
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29463.
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29464.
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The G1021A substitution in the RYR1 gene does not cosegregate with malignant hyperthermia susceptibility in a British pedigree. [electronic resource] by
- Adeokun, A M
- West, S P
- Ellis, F R
- Halsall, P J
- Hopkins, P M
- Foroughmand, A M
- Iles, D E
- Robinson, R L
- Stewart, A D
- Curran, J L
Producer: 19970508
In:
American journal of human genetics vol. 60
Availability: No items available.
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29465.
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High-resolution mapping and transcript identification at the progressive epilepsy with mental retardation locus on chromosome 8p. [electronic resource] by
- Ranta, S
- Lehesjoki, A E
- de Fatima Bonaldo, M
- Knowles, J A
- Hirvasniemi, A
- Ross, B
- de Jong, P J
- Soares, M B
- de la Chapelle, A
- Gilliam, T C
Producer: 19971106
In:
Genome research vol. 7
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29466.
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29467.
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29468.
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Vocal cord and pharyngeal weakness with autosomal dominant distal myopathy: clinical description and gene localization to 5q31. [electronic resource] by
- Feit, H
- Silbergleit, A
- Schneider, L B
- Gutierrez, J A
- Fitoussi, R P
- Réyès, C
- Rouleau, G A
- Brais, B
- Jackson, C E
- Beckmann, J S
- Seboun, E
Producer: 19990201
In:
American journal of human genetics vol. 63
Availability: No items available.
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29469.
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The PROP1 2-base pair deletion is a common cause of combined pituitary hormone deficiency. [electronic resource] by
- Cogan, J D
- Wu, W
- Phillips, J A
- Arnhold, I J
- Agapito, A
- Fofanova, O V
- Osorio, M G
- Bircan, I
- Moreno, A
- Mendonca, B B
Producer: 19981008
In:
The Journal of clinical endocrinology and metabolism vol. 83
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29470.
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Recurrent germline mutation in MSH2 arises frequently de novo. [electronic resource] by
- Desai, D C
- Lockman, J C
- Chadwick, R B
- Gao, X
- Percesepe, A
- Evans, D G
- Miyaki, M
- Yuen, S T
- Radice, P
- Maher, E R
- Wright, F A
- de La Chapelle, A
Producer: 20001116
In:
Journal of medical genetics vol. 37
Availability: No items available.
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29471.
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Chromosomal fragile site FRA16D and DNA instability in cancer. [electronic resource] by
- Mangelsdorf, M
- Ried, K
- Woollatt, E
- Dayan, S
- Eyre, H
- Finnis, M
- Hobson, L
- Nancarrow, J
- Venter, D
- Baker, E
- Richards, R I
Producer: 20000504
In:
Cancer research vol. 60
Availability: No items available.
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29473.
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29474.
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29476.
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29477.
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29478.
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29479.
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29480.
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