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Matoso Eunice

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Molecular cytogenetic characterisation of a mosaic add(12)(p13.3) with an inv dup(3)(q26.31 → qter) detected in an autistic boy
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Documents

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

Molecular cytogenetic characterisation of a mosaic add(12)(p13.3) with an inv dup(3)(q26.31 → qter) detected in an autistic boy Alternate Text
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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

Book

7 pages

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English

X-chromosome terminal deletion in a female with premature ovarian failure: Haploinsufficiency of X-linked genes as a possible explanation
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Documents

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

X-chromosome terminal deletion in a female with premature ovarian failure: Haploinsufficiency of X-linked genes as a possible explanation Alternate Text
Category

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

Book

7 pages

Flag

English

Alternate Text