alexa Katrin Ounap | OMICS International
ISSN: 2161-1041

Hereditary Genetics: Current Research
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Katrin Ounap

She is Clinical associate professor of genetics as well as of pediatrician. She represents Department of Genetics, United Laboratories, Tartu University Hospital, Estonia
Biography

Tartu University, Faculty of Medicine, paediatrics specialist in 1988,
post-diploma professional training:
03.1990 Russian Pediatrics and Children's Surgery Institute of Clinical Genetics specialty,
10.1992 Helsinki University Children's Clinic of the Clinical Genetics specialty,
04.1994 and 03.1996 of the Berlin Humboldt University Wirchowi Hospital Human Genetics Institute of Clinical Genetics specialty;
11.1996 Göteborg University Sahlgrenska Hospital Clinical Chemistry Department of hereditary metabolic diseases;
10-11.2002 at Dresden University of Technology, the Institute of Human Genetics, Clinical Genetics specialty

Research Interest

1. Clinical Genetics
2. Microdeletion syndromes
3. Hereditary metabolic diseases in Estonia: incidence, diagnosis and treatment

Publications

Outcome of Children with Marked Changes in Maternal Screening Tests and Normal Karyotype

Kai Muru, Mari-Anne Vals, Mari Sitska, Karin Asser, Pille Tammur, Olga Zilina, Tiia Reimand and Katrin Ounap

Research Article: Hereditary Genet 2014, 3:123

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