Documents Savoirs Molecular cytogenetic characterisation of a mosaic add(12)(p13.3) with an inv dup(3)(q26.31 → qter) detected in an autistic boy Carreira, Rodrigues Carlos, Backx Liesbeth, Vermeesch Joris, Weise Anja, Kosyakova Nadezda, Oliveira Guiomar, Matoso, Matoso Eunice, Melo
Documents Savoirs X-chromosome terminal deletion in a female with premature ovarian failure: Haploinsufficiency of X-linked genes as a possible explanation Matoso Eunice, Pinto Marta, Almeida Joana, Liehr Thomas, Carreira, Ferreira, Melo