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Preimplantation genetic diagnosis of DiGeorge syndrome.
Published in:
Molecular Human Reproduction, 1998, v. 4, n. 9, doi. 10.1093/molehr/4.9.871
By:
- Iwarsson, E;
- Iwarsson, E.;
- Ahrlund-Richter, L;
- Ahrlund-Richter, L.;
- Inzunza, J;
- Inzunza, J.;
- Fridstrom, M;
- Fridstrom, M.;
- Rosenlund, B;
- Rosenlund, B.;
- Hillensjo, T;
- Hillensjo, T.;
- Sjoblom, P;
- Sjoblom, P.;
- Nordenskjold, M;
- Nordenskjold, M.;
- Blennow, E;
- Blennow, E.
Publication type:
Article
Comparative genomic hybridization and karyotyping of human embryonic stem cells reveals the occurrence of an isodicentric X chromosome after long‐term cultivation.
Published in:
Molecular Human Reproduction, 2004, v. 10, n. 6, p. 461, doi. 10.1093/molehr/gah051
By:
- Inzunza, J.;
- Sahlén, S.;
- Holmberg, K.;
- Strömberg, A.‐M.;
- Teerijoki, H.;
- Blennow, E.;
- Hovatta, O.;
- Malmgren, H.
Publication type:
Article
Single cell CGH analysis reveals a high degree of mosaicism in human embryos from patients with balanced structural chromosome aberrations.
Published in:
Molecular Human Reproduction, 2002, v. 8, n. 5, p. 502, doi. 10.1093/molehr/8.5.502
By:
- Malmgren, H.;
- Sahlén, S.;
- Inzunza, J.;
- Aho, M.;
- Rosenlund, B.;
- Fridström, M.;
- Hovatta, O.;
- Ährlund-Richter, L.;
- Nordenskjöld, M.;
- Blennow, E.
Publication type:
Article
Preimplantation genetic diagnosis of a large pericentric inversion of chromosome 5.
Published in:
Molecular Human Reproduction, 1998, v. 4, n. 7, doi. 10.1093/molehr/4.7.719
By:
- Iwarsson, E;
- Åhrlund-Richter, L;
- Inzunza, J;
- Rosenlund, B;
- Fridström, M;
- Hillensjö, T;
- Sjöblom, P;
- Nordenskjöld, M;
- Blennow, E
Publication type:
Article
Improved structural characterization of chromosomal breakpoints using high resolution custom array-CGH.
Published in:
Clinical Genetics, 2010, v. 77, n. 6, p. 552, doi. 10.1111/j.1399-0004.2009.01341.x
By:
- Lindstrand, A.;
- Schoumans, J.;
- Gustavsson, P.;
- Hanemaaijer, N.;
- Malmgren, H.;
- Blennow, E.
Publication type:
Article
Detailed molecular and clinical characterization of three patients with 21q deletions.
Published in:
Clinical Genetics, 2010, v. 77, n. 2, p. 145, doi. 10.1111/j.1399-0004.2009.01289.x
By:
- Lindstrand, A.;
- Malmgren, H.;
- Sahlén, S.;
- Schoumans, J.;
- Nordgren, A.;
- Ergander, U.;
- Holm, E.;
- Anderlid, B. M.;
- Blennow, E.
Publication type:
Article
Concurrent microdeletion and duplication of 22q11.2.
Published in:
Clinical Genetics, 2008, v. 74, n. 1, p. 61, doi. 10.1111/j.1399-0004.2008.01008.x
By:
- Blennow, E.;
- Lagerstedt, K.;
- Malmgren, H.;
- Sahlén, S.;
- Schoumans, J.;
- Anderlid, B. M.
Publication type:
Article
Clinical outcome of treatment cycles using preimplantation genetic diagnosis for structural chromosomal abnormalities.
Published in:
2001
By:
- Fridström, Margareta;
- Ährlund-Richter, Lars;
- Iwarsson, Erik;
- Malmgren, Helena;
- Inzunza, José;
- Rosenlund, Björn;
- Sjöblom, Peter;
- Nordenskjöld, Magnus;
- Blennow, Elisabeth;
- Hovatta, Outi;
- Fridström, M;
- Ahrlund-Richter, L;
- Iwarsson, E;
- Malmgren, H;
- Inzunza, J;
- Rosenlund, B;
- Sjöblom, P;
- Nordenskjöld, M;
- Blennow, E;
- Hovatta, O
Publication type:
journal article
Application of single-needle blastomere biopsy in human preimplantation genetic diagnosis.
Published in:
Prenatal Diagnosis, 1998, v. 18, n. 13, p. 1381, doi. 10.1002/(SICI)1097-0223(199812)18:13<1381::AID-PD495>3.0.CO;2-N
By:
- Inzunza, J.;
- Iwarsson, E.;
- Fridström, M.;
- Rosenlund, B.;
- Sjöblom, P.;
- Hillensjö, T.;
- Blennow, E.;
- Jones, B.;
- Nordenskjöld, M.;
- Ährlund-Richter, I.
Publication type:
Article
Application of single-needle blastomere biopsy in human preimplantation genetic diagnosis.
Published in:
1998
By:
- Inzunza, J;
- Iwarsson, E;
- Fridström, M;
- Rosenlund, B;
- Sjöblom, P;
- Hillensjö, T;
- Blennow, E;
- Jones, B;
- Nordenskjöld, M;
- Ahrlund-Richter, L
Publication type:
journal article
Swedish survey on extra structurally abnormal chromosomes in 39 105 consecutive prenatal diagnoses: prevalence and characterization by fluorescence in situ hybridization.
Published in:
1994
By:
- Blennow, Elisabeth;
- Bui, The-Hung;
- Kristoffersson, Ulf;
- Vujic, Mihailo;
- Annerén, Göran;
- Holmberg, Eva;
- Nordenskjöld, Magnus;
- Blennow, E;
- Bui, T H;
- Kristoffersson, U;
- Vujic, M;
- Annerén, G;
- Holmberg, E;
- Nordenskjöld, M
Publication type:
journal article
In vitro culture conditions favoring selection of chromosomal abnormalities in human ES cellsM.P. Imreh and K. Gertow have contributed equally to this work.
Published in:
Journal of Cellular Biochemistry, 2006, v. 99, n. 2, p. 508, doi. 10.1002/jcb.20897
By:
- M.P. Imreh;
- K. Gertow;
- J. Cedervall;
- C. Unger;
- K. Holmberg;
- K. Szöke;
- L. Csöregh;
- G. Fried;
- S. Dilber;
- E. Blennow;
- L. Ährlund‐Richter
Publication type:
Article
The position of t(11;22)(q23;q11) constitutional translocation breakpoint is conserved among its carriers.
Published in:
Human Genetics, 2001, v. 109, n. 2, p. 167, doi. 10.1007/s004390100560
By:
- Tapia-Páez, I.;
- Kost-Alimova, M.;
- Hu, P.;
- Roe, B.;
- Blennow, E.;
- Fedorova, L.;
- Imreh, S.;
- Dumanski, J.
Publication type:
Article
One-cell biopsy significantly improves the outcome of preimplantation genetic diagnosis (PGD) treatment: retrospective analysis of 569 PGD cycles at the Stockholm PGD centre.
Published in:
2012
By:
- Haapaniemi Kouru K;
- Malmgren H;
- Nordenskjöld M;
- Fridström M;
- Csemiczky G;
- Blennow E
Publication type:
Journal Article
One-cell biopsy significantly improves the outcome of preimplantation genetic diagnosis (PGD) treatment: retrospective analysis of 569 PGD cycles at the Stockholm PGD centre.
Published in:
Human Reproduction, 2012, v. 27, n. 9, p. 2843, doi. 10.1093/humrep/des235
By:
- Haapaniemi Kouru, K.;
- Malmgren, H.;
- Nordenskjöld, M.;
- Fridström, M.;
- Csemiczky, G.;
- Blennow, E.
Publication type:
Article
Children and adults with acute lymphoblastic leukaemia have similar gene expression profiles.
Published in:
European Journal of Haematology, 2005, v. 74, n. 6, p. 466, doi. 10.1111/j.1600-0609.2005.00433.x
By:
- Kuchinskaya, E.;
- Heyman, M.;
- Grandér, D.;
- Linderholm, M.;
- Söderhäll, S.;
- Zaritskey, A.;
- Nordgren, A.;
- Porwit-MacDonald, A.;
- Zueva, E.;
- Pawitan, Y.;
- Corcoran, M.;
- Nordenskjöld, M.;
- Blennow, E.
Publication type:
Article
A culture system using human foreskin fibroblasts as feeder cells allows production of human embryonic stem cells.
Published in:
Human Reproduction, 2003, v. 18, n. 7, p. 1404
By:
- L. Ährlund-Richter;
- O. Hovatta;
- M. Mikkola;
- K. Gertow;
- A-M. Strömberg;
- J. Inzunza;
- J. Hreinsson;
- B. Rozell;
- E. Blennow;
- M. Andäng
Publication type:
Article
Patients' experiences of preimplanlation genetic diagnosis in Sweden.
Published in:
Reproductive BioMedicine Online (Reproductive Healthcare Limited), 2008, v. 16, p. S-31
By:
- H., Malmgren;
- C., Lampic;
- J., Stevic;
- L. B., Nilsson;
- M. G., Hansson;
- E., Iwarsson;
- M., Fridström;
- E., Blennow
Publication type:
Article
The frequency and prognostic impact of dic(9;20)(p13.2;q11.2) in childhood B-cell precursor acute lymphoblastic leukemia: results from the NOPHO ALL-2000 trial.
Published in:
Leukemia (08876924), 2011, v. 25, n. 4, p. 622, doi. 10.1038/leu.2010.318
By:
- Zachariadis, V.;
- Gauffin, F.;
- Kuchinskaya, E.;
- Heyman, M.;
- Schoumans, J.;
- Blennow, E.;
- Gustafsson, B.;
- Barbany, G.;
- Golovleva, I.;
- Ehrencrona, H.;
- Cavelier, L.;
- Palmqvist, L.;
- Lönnerholm, G.;
- Nordenskjöld, M.;
- Johansson, B.;
- Forestier, E.;
- Nordgren, A.
Publication type:
Article
Tiling-resolution array-CGH reveals the pattern of DNA copy number alterations in acute lymphoblastic leukemia with 21q amplification: the result of telomere dysfunction and breakage/fusion/breakage cycles?
Published in:
2007
By:
- Kuchinskaya, E.;
- Nordgren, A.;
- Heyman, M.;
- Schoumans, J.;
- Corcoran, M.;
- Staaf, J.;
- Borg, Å;
- Söderhäll, S.;
- Grandér, D.;
- Nordenskjöld, M.;
- Blennow, E.
Publication type:
Letter
Molecular analysis of 1p36 breakpoints in two Merkel cell carcinomas.
Published in:
Genes, Chromosomes & Cancer, 1998, v. 23, n. 1, p. 67, doi. 10.1002/(SICI)1098-2264(199809)23:1<67::AID-GCC10>3.0.CO;2-B
By:
- Van Gele, M.;
- Van Roy, N.;
- Ronan, S. G.;
- Messiaen, L.;
- Vandesompele, J.;
- Geerts, M. L.;
- Naeyaert, J. M.;
- Blennow, E.;
- Bar-Am, I.;
- Das Gupta, T. K.;
- van der Drift, P.;
- Versteeg, R.;
- Leonard, J. H.;
- Speleman, F.
Publication type:
Article

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