Chromosomes, Human, Pair 19/ geneticsRefine your research by the most used items
Author / Editor
- Antonarakis, Stylianos (2)
- Mehenni, H. (2)
- Bermejo-Fenoll, A. (1)
- Bhardwaj, K. (1)
- Bhardwaj, S. S. (1)
- Blouin, Jean-Louis (1)
- Dixit, V. B. (1)
- Doyle, J. (1)
- Hoffman, S. (1)
- Krieg, T. (1)
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remove all| Title | Authors / Editors | Date | |
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Gene for the human transmembrane-type protein tyrosine phosphatase H (PTPRH): genomic structure, fine-mapping and its exclusion as a candidate for Peutz-Jeghers syndrome | Marneros, A. G.; Mehenni, H.; Reichenberger, E.; Antonarakis, Stylianos; ... Olsen, B. R. | 2001 |
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Peutz-Jeghers syndrome: confirmation of linkage to chromosome 19p13.3 and identification of a potential second locus, on 19q13.4 | Mehenni, H.; Blouin, Jean-Louis; Radhakrishna, U.; Bhardwaj, S. S.; ... Antonarakis, Stylianos | 1997 |
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Locations of human and mouse genes encoding the RFX1 and RFX2 transcription factor proteins | Doyle, J.; Hoffman, S.; Ucla, C.; Reith, Walter; ... Stubbs, L. | 1996 |
