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Catarina Lundin

Titel

överläkare

Organisation

Avdelningen för klinisk genetik

Telefon 046-173349

E-post Catarina [dot] Lundin [at] med [dot] lu [dot] se

Publikationer (hämtat ur Lunds universitets publikationsdatabas)

författare

2013
- Submicroscopic genomic imbalances in burkitt lymphomas/leukemias: Association with age and further evidence that 8q24/MYC translocations are not sufficient for leukemogenesis.
2012
- High frequency of BTG1 deletions in acute lymphoblastic leukemia in children with down syndrome.
2011
- Ultrasonographic findings in spontaneous miscarriage: relation to euploidy and aneuploidy
- t(9;11)(p22;p15) NUP98/PSIP1 is a poor prognostic marker associated with de novo acute myeloid leukaemia expressing both mature and immature surface antigens.
2009
- B-cell precursor t(8;14)(q11;q32)-positive acute lymphoblastic leukemia in children is strongly associated with Down syndrome or with a concomitant Philadelphia chromosome.
- Tiling resolution array-based comparative genomic hybridisation analyses of acute lymphoblastic leukaemias in children with Down syndrome reveal recurrent gain of 8q and deletions of 7p and 9p.
2007
- Tiling resolution array CGH of dic(7;9)(p11 approximately 13;p11 approximately 13) in B-cell precursor acute lymphoblastic leukemia reveals clustered breakpoints at 7p11.2 approximately 12.1 and 9p13.1.
1998
- Cytogenetic studies of benign breast lesions

Visa detaljerad publikationslista

Box 117, 221 00 LUND
Telefon 046-222 00 00 (växel)
Telefax 046-222 47 20
lu [at] lu [dot] se

Fakturaadress: Box 188, 221 00 LUND
Organisationsnummer: 202100-3211
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