Chromosomes, human, pair 6/ geneticsRefine your research by the most used items
Author / Editor
- Antonarakis, Stylianos (3)
- Bottani, Armand (2)
- Morris, Michael Andréw (2)
- Addor, M. C. (1)
- Al-Ali, M. T. (1)
- Al-Khaja, Najib (1)
- Beckmann, J. S. (1)
- Bena, Frédérique (1)
- Besuchet Schmutz, Nathalie (1)
- Bittencourt, M. C. (1)
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remove all| Title | Authors / Editors | Date | |
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Subtelomeric 6p deletion: clinical and array-CGH characterization in two patients | Martinet, Danielle; Filges, Isabel; Besuchet Schmutz, Nathalie; Morris, Michael Andréw; ... Bena, Frédérique | 2008 |
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Genomewide linkage scan for split-hand/foot malformation with long-bone deficiency in a large Arab family identifies two novel susceptibility loci on chromosomes 1q42.2-q43 and 6q14.1 | Naveed, Mohammed; Nath, S. K.; Gaines, Mathew; Al-Ali, M. T.; ... Radhakrishna, Uppala | 2007 |
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Fortuitous detection of uniparental isodisomy of chromosome 6 | Bittencourt, M. C.; Morris, Michael Andréw; Chabod, J.; Gos, A.; ... Tiberghien, P. | 1997 |
