Genetic Diseases, Inborn/geneticsRefine your research by the most used items
Author / Editor
- Antonarakis, Stylianos (3)
- Bairoch, Amos Marc (1)
- Beckmann, J. S. (1)
- Boeckmann, Brigitte (1)
- Borel, Christelle (1)
- Burmeister, M. (1)
- Cann, H. (1)
- Chakravarti, A. (1)
- Cheung, Fanny (1)
- Creau, N. (1)
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remove all| Title | Authors / Editors | Date | |
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Evaluation of PRDM9 variation as a risk factor for recurrent genomic disorders and chromosomal non-disjunction | Borel, Christelle; Cheung, Fanny; Stewart, Helen; Koolen, David A; ... Sharp, Andrew J | 2012 |
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Epistatic selection between coding and regulatory variation in human evolution and disease | Lappalainen, Tuuli Emilia; Montgomery, Stephen; Nica, Alexandra; Dermitzakis, Emmanouil | 2011 |
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Copy number variants and genetic traits: closer to the resolution of phenotypic to genotypic variability | Beckmann, J. S.; Estivill, Xavier; Antonarakis, Stylianos | 2007 |
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Guidelines for human gene nomenclature (1997). HUGO Nomenclature Committee | White, J. A.; McAlpine, P. J.; Antonarakis, Stylianos; Cann, H.; ... Povey, S. | 1997 |
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The SWISS-PROT protein sequence data bank: current status | Bairoch, Amos Marc; Boeckmann, Brigitte | 1994 |
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Report of the Fourth International Workshop on Human Chromosome 21 | Delabar, J. M.; Creau, N.; Sinet, P. M.; Ritter, O.; ... Patterson, D. | 1993 |
