Catarina Lundin

Catarina Lundin

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Catarina Lundin

Catarina Lundin

Publications by authors named "Catarina Lundin"

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14Publications

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Danon disease presenting with early onset of hypertrophic cardiomyopathy and peripheral pigmentary retinal dystrophy in a female with a novel mosaic mutation in the gene.

Ophthalmic Genet 2019 Jun 2;40(3):227-236. Epub 2019 Jul 2.

a Department of Clinical Sciences Lund, Ophthalmology , Lund University, Skane University Hospital , Lund , Sweden.

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http://dx.doi.org/10.1080/13816810.2019.1627464DOI Listing
June 2019

Constitutional and somatic deletions of the Williams-Beuren syndrome critical region in non-Hodgkin lymphoma.

J Hematol Oncol 2014 Nov 7;7:82. Epub 2014 Nov 7.

Laboratory of Cellular and Molecular Biology, University Hospital of Besançon, 1 Bd Fleming, Batiment Diaclone, Besançon, France.

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http://dx.doi.org/10.1186/s13045-014-0082-4DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4228180PMC
November 2014

Submicroscopic genomic imbalances in Burkitt lymphomas/leukemias: association with age and further evidence that 8q24/MYC translocations are not sufficient for leukemogenesis.

Genes Chromosomes Cancer 2013 Apr 8;52(4):370-7. Epub 2012 Dec 8.

Department of Clinical Genetics, University and Regional Laboratories, Skåne University Hospital, Lund University, Lund, Sweden.

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http://dx.doi.org/10.1002/gcc.22034DOI Listing
April 2013

High frequency of BTG1 deletions in acute lymphoblastic leukemia in children with down syndrome.

Genes Chromosomes Cancer 2012 Feb 10;51(2):196-206. Epub 2011 Nov 10.

Department of Clinical Genetics, University and Regional Laboratories, Skåne University Hospital, Lund University, Sweden.

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http://dx.doi.org/10.1002/gcc.20944DOI Listing
February 2012

Ultrasonographic findings in spontaneous miscarriage: relation to euploidy and aneuploidy.

Fertil Steril 2011 Jan 17;95(1):221-4. Epub 2010 Jul 17.

Department of Women's and Children's Health, Uppsala University, and Uppsala Hospital, Uppsala, Sweden.

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http://dx.doi.org/10.1016/j.fertnstert.2010.06.018DOI Listing
January 2011

[Hereditary risk of sudden cardiac death--genetic investigation of the family].

Lakartidningen 2009 Apr 7-21;106(15-16):1089-93

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June 2009

Chromosomal anomalies in first-trimester miscarriages.

Acta Obstet Gynecol Scand 2005 Nov;84(11):1103-7

Department of Women and Child Health, Uppsala University, Uppsala, Sweden.

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http://dx.doi.org/10.1111/j.0001-6349.2005.00882.xDOI Listing
November 2005

Trisomy 4q syndrome: presentation of a new case and review of the literature.

Ann Genet 2002 Apr-Jun;45(2):53-7

Unit of Clinical Genetics, Department of Genetics and Pathology, Uppsala University, Sweden

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February 2003