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Pretransplant HLA mistyping in diagnostic samples of acute myeloid leukemia patients due to acquired uniparental disomy. [electronic resource] by
- Dubois, V
- Sloan-Béna, F
- Cesbron, A
- Hepkema, B G
- Gagne, K
- Gimelli, S
- Heim, D
- Tichelli, A
- Delaunay, J
- Drouet, M
- Jendly, S
- Villard, J
- Tiercy, J-M
Producer: 20121113
In:
Leukemia vol. 26
Availability: No items available.
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11.
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No evidence for the presence of genetic variants predisposing to psychotic disorders on the non-deleted 22q11.2 allele of VCFS patients. [electronic resource] by
- Guipponi, M
- Santoni, F
- Schneider, M
- Gehrig, C
- Bustillo, X B
- Kates, W R
- Morrow, B
- Armando, M
- Vicari, S
- Sloan-Béna, F
- Gagnebin, M
- Shashi, V
- Hooper, S R
- Eliez, S
- Antonarakis, S E
Producer: 20171116
In:
Translational psychiatry vol. 7
Availability: No items available.
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12.
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Adolescence is the starting point of sex-dichotomous COMT genetic effects. [electronic resource] by
- Sannino, S
- Padula, M C
- Managò, F
- Schaer, M
- Schneider, M
- Armando, M
- Scariati, E
- Sloan-Bena, F
- Mereu, M
- Pontillo, M
- Vicari, S
- Contarini, G
- Chiabrera, C
- Pagani, M
- Gozzi, A
- Eliez, S
- Papaleo, F
Producer: 20180319
In:
Translational psychiatry vol. 7
Availability: No items available.
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13.
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Experience of a multidisciplinary task force with exome sequencing for Mendelian disorders. [electronic resource] by
- Fokstuen, S
- Makrythanasis, P
- Hammar, E
- Guipponi, M
- Ranza, E
- Varvagiannis, K
- Santoni, F A
- Albarca-Aguilera, M
- Poleggi, M E
- Couchepin, F
- Brockmann, C
- Mauron, A
- Hurst, S A
- Moret, C
- Gehrig, C
- Vannier, A
- Bevillard, J
- Araud, T
- Gimelli, S
- Stathaki, E
- Paoloni-Giacobino, A
- Bottani, A
- Sloan-Béna, F
- Sizonenko, L D'Amato
- Mostafavi, M
- Hamamy, H
- Nouspikel, T
- Blouin, J L
- Antonarakis, S E
Producer: 20171127
In:
Human genomics vol. 10
Availability: No items available.
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