Familial t(6;21)(p21.1;p13) translocation associated with male-only sterility
Paoloni-Giacobino, A, Kern1, I, Rumpler, Y, Djlelati, R, Morris, MA, Dahoun, SP
Published in Clinical genetics (01.10.2000)
Published in Clinical genetics (01.10.2000)
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Journal Article
A case of (X;15) translocation diagnosed as a paracentric inversion of Xp: diagnostic revision with FISH
Paoloni-Giacobino, A, Lespinasse, J, Moix, I, Dahoun, S.P
Published in Annales de génétique (01.07.2001)
Published in Annales de génétique (01.07.2001)
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Journal Article
A proven case of materno-foetal transfusion determined by cytogenetic and DNA analysis
Paoloni-Giacobino, A, Dutoit, Mh, Morris, Ma, Dahoun, Sp
Published in Clinical genetics (01.04.1999)
Published in Clinical genetics (01.04.1999)
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Journal Article
No Evidence for an Effect of COMT Val158Met Genotype on Executive Function in Patients With 22q11 Deletion Syndrome
Glaser, Bronwyn, Debbane, Martin, Hinard, Christine, Morris, Michael A., Dahoun, Sophie P., Antonarakis, Stylianos E., Eliez, Stephan
Published in The American journal of psychiatry (01.03.2006)
Published in The American journal of psychiatry (01.03.2006)
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Journal Article
Language skills in children with velocardiofacial syndrome (deletion 22q11.2)
Glaser, Bronwyn, Mumme, Donna L., Blasey, Christine, Morris, Michael A., Dahoun, Sophie P., Antonarakis, Stylianos E., Reiss, Allan L., Eliez, Stephan
Published in The Journal of pediatrics (01.06.2002)
Published in The Journal of pediatrics (01.06.2002)
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Journal Article