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J Steinhard

Showing results (21-30 of 24) with videos related to

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Zeitschrift Fur Geburtshilfe Und Neonatologie|July 5, 2005
[Fetal nephro-/uropathy: a retrospective analysis of 124 cases seen in the period from 1996 to 2002]M Bulla, E Kuwertz-Bröking, S Fründ, et al.
Ultrasound in Obstetrics & Gynecology : the Official Journal of the International Society of Ultrasound in Obstetrics and Gynecology|November 25, 2014
Evaluation of right ventricular function in fetuses with hypoplastic left heart syndrome using tissue Doppler techniquesR Axt-Fliedner, O Graupner, A Kawecki, et al.
Ultrasound in Obstetrics & Gynecology : the Official Journal of the International Society of Ultrasound in Obstetrics and Gynecology|July 4, 2015
Evaluation of right ventricular function in fetal hypoplastic left heart syndrome by color tissue Doppler imagingO Graupner, C Enzensberger, L Wieg, et al.
Human Mutation|March 25, 1999
Peutz-Jeghers syndrome: four novel inactivating germline mutations in the STK11 gene. Mutations in brief no. 227. OnlineR Kruse, S Uhlhaas, C Lamberti, et al.
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Showing results (21-30 of 24) with videos related to

Sort By:
Pageof 3
You have reached the last page of results.This site can display upto 24 results.
Zeitschrift Fur Geburtshilfe Und Neonatologie|July 5, 2005
[Fetal nephro-/uropathy: a retrospective analysis of 124 cases seen in the period from 1996 to 2002]M Bulla, E Kuwertz-Bröking, S Fründ, et al.
Ultrasound in Obstetrics & Gynecology : the Official Journal of the International Society of Ultrasound in Obstetrics and Gynecology|November 25, 2014
Evaluation of right ventricular function in fetuses with hypoplastic left heart syndrome using tissue Doppler techniquesR Axt-Fliedner, O Graupner, A Kawecki, et al.
Ultrasound in Obstetrics & Gynecology : the Official Journal of the International Society of Ultrasound in Obstetrics and Gynecology|July 4, 2015
Evaluation of right ventricular function in fetal hypoplastic left heart syndrome by color tissue Doppler imagingO Graupner, C Enzensberger, L Wieg, et al.
Human Mutation|March 25, 1999
Peutz-Jeghers syndrome: four novel inactivating germline mutations in the STK11 gene. Mutations in brief no. 227. OnlineR Kruse, S Uhlhaas, C Lamberti, et al.
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