Familial t(6;21)(p21.1;p13) translocation associated with male-only sterility von Paoloni-Giacobino, A, Kern1, I, Rumpler, Y, Djlelati, R, Morris, MA, Dahoun, SP

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Amplification of a pseudogene cassette underlies euchromatic variation of 16p at the cytogenetic level von BARBER, J. C. K, REED, C. J, DAHOUN, S. P, JOYCE, C. A

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Fetus with a 9q22q34 interstitial deletion and hygroma von Paoloni-Giacobino, A., Floris, E., Dahoun, S. P.

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Prenatal supernumerary r(16) chromosome characterized by multiprobe FISH with normal pregnancy outcome von Paoloni-Giacobino, A, Morris, M A, Dahoun, S P

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A case of 45,X Turner syndrome with spontaneous ovulation proven by ultrasonography von Paoloni-Giacobino, A., Dahoun, S. P., Sizonenko, P. C., Stalberg, A., Chardonnens, D., Campana, A.

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A case of (X;15) translocation diagnosed as a paracentric inversion of Xp: diagnostic revision with FISH von Paoloni-Giacobino, A, Lespinasse, J, Moix, I, Dahoun, S.P

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A proven case of materno-foetal transfusion determined by cytogenetic and DNA analysis von Paoloni-Giacobino, A, Dutoit, Mh, Morris, Ma, Dahoun, Sp

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No Evidence for an Effect of COMT Val158Met Genotype on Executive Function in Patients With 22q11 Deletion Syndrome von Glaser, Bronwyn, Debbane, Martin, Hinard, Christine, Morris, Michael A., Dahoun, Sophie P., Antonarakis, Stylianos E., Eliez, Stephan

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Language skills in children with velocardiofacial syndrome (deletion 22q11.2) von Glaser, Bronwyn, Mumme, Donna L., Blasey, Christine, Morris, Michael A., Dahoun, Sophie P., Antonarakis, Stylianos E., Reiss, Allan L., Eliez, Stephan

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Parental Origin of the Deletion 22q11.2 and Brain Development in Velocardiofacial Syndrome: A Preliminary Study von Eliez, Stephan, Antonarakis, Stylianos E, Morris, Michael A, Dahoun, Sophie P, Reiss, Allan L

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Prenatal supernumeray r(16) chromosome characterized by multiprobe FISH with normal pregnancy outcome von Paoloni-Giacobino, A., Morris, M. A., Dahoun, S. P.

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Anomalies chromosomiques des spermatozoïdes von PAOLONI-GIACOBINO, A, DAHOUN, S. P

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Syndrome de Turner et fertilité : à propos d'un cas d'ovulation spontanée chez une patiente avec un caryotype 45, X von PAOLONI-GIACOBINO, A, SIZONENKO, P. C, DAHOUN, S. P, CAMPANA, A

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Fetus with a 9q22q34 interstitial deletion and hygroma von Paoloni-Giacobino, A, Floris, E, Dahoun, S P

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Prenatal supernumerary r(16) chromosome characterized by multiprobe FISH with normal pregnancy outcome von Paoloni-Giacobino, A, Morris, M A, Dahoun, S P

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Complementarities of high energy WAXS and Raman spectroscopy measurements to study the crystalline phase orientation in polypropylene blends during tensile test von Ponçot, M., Martin, J., Chaudemanche, S., Ferry, O., Schenk, T., Tinnes, J.P., Chapron, D., Royaud, I., Dahoun, A., Bourson, P.

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Variability in Action Selection Relates to Striatal Dopamine 2/3 Receptor Availability in Humans: A PET Neuroimaging Study Using Reinforcement Learning and Active Inference Models von Adams, Rick A, Moutoussis, Michael, Nour, Matthew M, Dahoun, Tarik, Lewis, Declan, Illingworth, Benjamin, Veronese, Mattia, Mathys, Christoph, de Boer, Lieke, Guitart-Masip, Marc, Friston, Karl J, Howes, Oliver D, Roiser, Jonathan P

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Computational design of orthogonal membrane receptor-effector switches for rewiring signaling pathways von Young, M., Dahoun, T., Sokrat, B., Arber, C., Chen, K. M., Bouvier, M., Barth, P.

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The relationship between childhood trauma, dopamine release and dexamphetamine-induced positive psychotic symptoms: a [11C]-(+)-PHNO PET study von Dahoun, Tarik, Nour, Matthew M., McCutcheon, Robert A., Adams, Rick A., Bloomfield, Michael A. P., Howes, Oliver D.

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A polygenic score indexing a DRD2-related co-expression network is associated with striatal dopamine function von D’Ambrosio, Enrico, Pergola, Giulio, Pardiñas, Antonio F., Dahoun, Tarik, Veronese, Mattia, Sportelli, Leonardo, Taurisano, Paolo, Griffiths, Kira, Jauhar, Sameer, Rogdaki, Maria, Bloomfield, Michael A. P., Froudist-Walsh, Sean, Bonoldi, Ilaria, Walters, James T. R., Blasi, Giuseppe, Bertolino, Alessandro, Howes, Oliver D.

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