Pille Tammur

https://www.etis.ee/CV/Pille_Tammur/est
24.02.1963
+3727422183
+37253319036
pille.tammur@kliinikum.ee

Teenistuskäik

Haridustee
1981–1987   
Tartu Ülikool, bioloogia-geograafia teaduskond, bioloog

Publikatsioonid

Klass
Aasta
Publikatsioon
 
5.1.
2007
Kuuse, K., Tammur, P., Zordania, R., Õunap, K. (2007). Subtelomeric monosomy 6p and trisomy 22q13.3 in a dysmorphic and mentally retarded boy. Chromosome Research: 6th European Cytogenetics Conference Istanbul, TURKEY, JUL 07-10, 2007. Kluwer Academic Publishers, 60−60. (15(Suppl.1)).
1.1.
2006
Weimer, J.; Metzke-Heidemann, S.; Plendl, H.; Caliebe, A.; Grunewald, R.; Õunap, K.; Tammur, P.; Jonat, W.; Bartsch, O.; Siebert, R.; Arnold, N. (2006). Characterization of two supernumerary marker chromosomes in a patient with signs of Klinefelter syndrome, mild facial anomalies, and severe speech delay. American Journal of Medical Genetics Part A, 140A (5), 488−495.
1.1.
2005
Ounap, K.; Ilus, T.; Laidre, P.; Uibo, O.; Tammur, P.; Bartsch, O. (2005). A new case of 2q duplication supports either a locus for orofacial clefting between markers D2S1897 and D2S2023 or a locus for cleft palate only on chromosome 2q13-q21. American Journal of Medical Genetics Part A, 137A (3), 323−327.
5.2.
2004
Teek, R.; Õunap, K.; Zordania, R.; Zõrjanova, T.; Tammur, P.; Bartsch, O. (2004). Case report: Boy with severe hypotonia, hypogenitalism, chronic interstitial pneumonia, and partial X disomy, karyotype 46,X,der(Y)t(X;Y)(q28;q11.2). European Journal of Human Genetics, 12 (Suppl 1), 129.
14.10.2019

Pille Tammur

https://www.etis.ee/CV/Pille_Tammur/eng
24.02.1963
+3727422183
+37253319036
pille.tammur@kliinikum.ee

Career

Education
1981–1987   
Tartu University, biologist

Publications

Category
Year
Publication
 
5.1.
2007
Kuuse, K., Tammur, P., Zordania, R., Õunap, K. (2007). Subtelomeric monosomy 6p and trisomy 22q13.3 in a dysmorphic and mentally retarded boy. Chromosome Research: 6th European Cytogenetics Conference Istanbul, TURKEY, JUL 07-10, 2007. Kluwer Academic Publishers, 60−60. (15(Suppl.1)).
1.1.
2006
Weimer, J.; Metzke-Heidemann, S.; Plendl, H.; Caliebe, A.; Grunewald, R.; Õunap, K.; Tammur, P.; Jonat, W.; Bartsch, O.; Siebert, R.; Arnold, N. (2006). Characterization of two supernumerary marker chromosomes in a patient with signs of Klinefelter syndrome, mild facial anomalies, and severe speech delay. American Journal of Medical Genetics Part A, 140A (5), 488−495.
1.1.
2005
Ounap, K.; Ilus, T.; Laidre, P.; Uibo, O.; Tammur, P.; Bartsch, O. (2005). A new case of 2q duplication supports either a locus for orofacial clefting between markers D2S1897 and D2S2023 or a locus for cleft palate only on chromosome 2q13-q21. American Journal of Medical Genetics Part A, 137A (3), 323−327.
5.2.
2004
Teek, R.; Õunap, K.; Zordania, R.; Zõrjanova, T.; Tammur, P.; Bartsch, O. (2004). Case report: Boy with severe hypotonia, hypogenitalism, chronic interstitial pneumonia, and partial X disomy, karyotype 46,X,der(Y)t(X;Y)(q28;q11.2). European Journal of Human Genetics, 12 (Suppl 1), 129.
14.10.2019
Detailne otsing
  • Leitud 1 kirjet
ProgrammLiikNumberNimiProjekti algusProjekti lõppVastutav täitjaAsutusFinantseerijapoolne rahastamine
ETFETF8175Düsmorfoloogia. Kaasasündinud düsmorfsete tunnuste, kasvu- ja arenguhäiretega laste uurimine01.01.201031.12.2013Katrin ÕunapTartu Ülikool, Arstiteaduskond70 559,61 EUR