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- Eeva Maria Therman (* 4. August 1916 in Helsinki; † 11. Juni 2004 ebenda) war eine finnisch-amerikanische Zytogenetikerin. Bekannt wurde sie durch Untersuchungen des menschlichen X-Chromosoms, der Chromosomenveränderungen bei malignen Erkrankungen sowie durch ein Standardwerk über menschliche Chromosomen. (de)
- Eeva Maria Therman-Patau (1916–2004) was a Finnish-born American geneticist. She worked to characterize the effects and cytogenetics of trisomy 13 and trisomy 18, two rare and usually fatal genetic disorders caused by an extra copy of chromosome 13 and 18, respectively.Her works include Human Chromosomes: Structure, Behavior, Effects, a textbook on cytogenetics which is in its 4th edition. Her research specialties included X-inactivation in mammals and chromosomal abnormalities in cancer. She received her PhD from the University of Helsinki in 1947. She emigrated to the United States in 1958, and shortly thereafter began to work as a research assistant in Klaus Patau's laboratory in the Department of Genetics at the University of Wisconsin–Madison. Three years later, she married Patau. Due to university hiring rules, she was unable to become faculty until Patau's death in 1975. She retired in 1986, and returned to Finland in 2002. (en)
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- 4386 (xsd:nonNegativeInteger)
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- Portrait of Eeva Therman as a young woman from her obituary in Helsingin Sanomat, written by her friend and colleague Petter Portin. (en)
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- Genetics of trisomy 13 and trisomy 18 (en)
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- Finland, United States (en)
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- Heikki Suomalainen (en)
- Klaus Patau (en)
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- Eeva Maria Therman (* 4. August 1916 in Helsinki; † 11. Juni 2004 ebenda) war eine finnisch-amerikanische Zytogenetikerin. Bekannt wurde sie durch Untersuchungen des menschlichen X-Chromosoms, der Chromosomenveränderungen bei malignen Erkrankungen sowie durch ein Standardwerk über menschliche Chromosomen. (de)
- Eeva Maria Therman-Patau (1916–2004) was a Finnish-born American geneticist. She worked to characterize the effects and cytogenetics of trisomy 13 and trisomy 18, two rare and usually fatal genetic disorders caused by an extra copy of chromosome 13 and 18, respectively.Her works include Human Chromosomes: Structure, Behavior, Effects, a textbook on cytogenetics which is in its 4th edition. Her research specialties included X-inactivation in mammals and chromosomal abnormalities in cancer. (en)
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- Eeva Therman (de)
- Eeva Therman (en)
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