Publications by authors named "Hans-Christoph Duba"

26Publications

Somatic mosaic monosomy 7 and UPD7q in a child with MIRAGE syndrome caused by a novel SAMD9 mutation.

Pediatr Blood Cancer 2019 04 19;66(4):e27589. Epub 2018 Dec 19.

Department of Medical Genetics, Kepler University Hospital, Linz, Austria.

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http://dx.doi.org/10.1002/pbc.27589DOI Listing
April 2019

Cleft lip/palate and hereditary diffuse gastric cancer: report of a family harboring a CDH1 c.687 + 1G > A germline mutation and review of the literature.

Fam Cancer 2019 04;18(2):253-260

Laboratory for Molecular Biology and Tumor Cytogenetics, Department of Internal Medicine I, Ordensklinikum Linz Barmherzige Schwestern, Seilerstätte 4, 4010, Linz, Austria.

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http://dx.doi.org/10.1007/s10689-018-0111-5DOI Listing
April 2019

Chromosomal Aneuploidies and Early Embryonic Developmental Arrest.

Int J Fertil Steril 2015 Oct-Dec;9(3):346-53. Epub 2015 Oct 31.

Landes-Frauen-und Kinderklinik Linz, Department of Human Genetics, Krankenhausstraße, Linz, Austria ; Johannes Kepler University, Faculty of Medicine, Linz, Austria.

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4671381PMC
http://dx.doi.org/10.22074/ijfs.2015.4550DOI Listing
December 2015

Quantitative and qualitative trophectoderm grading allows for prediction of live birth and gender.

J Assist Reprod Genet 2016 Jan 14;33(1):49-57. Epub 2015 Nov 14.

Department of Gynecological Endocrinology and Kinderwunsch Zentrum, Landes- Frauen- und Kinderklinik, Krankenhausstr. 26-30, 4020, Linz, Upper Austria, Austria.

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http://dx.doi.org/10.1007/s10815-015-0609-9DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4717145PMC
January 2016

Disruption of the ARID1B and ADAMTS6 loci due to a t(5;6)(q12.3;q25.3) in a patient with developmental delay.

Am J Med Genet A 2014 Dec 22;164A(12):3126-31. Epub 2014 Sep 22.

Laboratory for Molecular Biology and Tumor Cytogenetics, Department of Internal Medicine I, Hospital Barmherzige Schwestern Linz, Upper Austria, Austria.

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http://dx.doi.org/10.1002/ajmg.a.36738DOI Listing
December 2014

Combined Dup(7)(q22.1q32.2), Inv(7)(q31.31q31.33), and Ins(7;19)(q22.1;p13.2p13.2) in a 12-year-old boy with developmental delay and various dysmorphism.

Eur J Med Genet 2013 Jul 19;56(7):383-8. Epub 2013 Apr 19.

Division of Human Genetics, Department of Medical Genetics, Molecular and Clinical Pharmacology, Innsbruck Medical University, Schoepfstr. 41, A-6020 Innsbruck, Austria.

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http://dx.doi.org/10.1016/j.ejmg.2013.04.003DOI Listing
July 2013

Labelling of human adipose-derived stem cells for non-invasive in vivo cell tracking.

Cell Tissue Bank 2007 25;8(3):163-77. Epub 2006 Oct 25.

Red Cross Blood Transfusion Service of Upper Austria, Blumauerstr. 3-5, Linz, A-4020, Austria.

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http://dx.doi.org/10.1007/s10561-006-9027-7DOI Listing
October 2007

High rate of molecular alteration in histologically tumour-free bronchial epithelium of NSCLC patients detected by multicolour fluorescence in situ hybridisation.

Oncol Rep 2006 May;15(5):1233-40

Department of Internal Medicine, Medical University Innsbruck, A-6020 Innsbruck, Austria.

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May 2006

FISH cytogenetics and prognosis in breast and non-small cell lung cancers.

Cytometry B Clin Cytom 2004 Nov;62(1):52-6

Department of Internal Medicine, Division of Hematology and Oncology, Medical University of Innsbruck, Innsbruck, Austria.

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http://dx.doi.org/10.1002/cyto.b.20023DOI Listing
November 2004

Muellerian aplasia associated with ring chromosome 8p12q12 mosaicism.

Am J Med Genet A 2003 Jan;116A(3):290-4

Institut für Medizinische Biologie und Humangenetik, Universität Innsbruck, Austria.

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http://dx.doi.org/10.1002/ajmg.a.10902DOI Listing
January 2003

Hepatosplenic gammadelta-T-cell lymphoma with leukemic course after renal transplantation.

Hum Pathol 2002 Feb;33(2):253-8

Division of Haematology and Oncology, University Hospital Innsbruck, Austria.

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http://dx.doi.org/10.1053/hupa.2002.31301DOI Listing
February 2002