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R Herva

Showing results (41-50 of 106) with videos related to

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Clinical Genetics|July 1, 1983
Trisomy 10p produced by recombination involving complex paternal translocation between chromosomes 1 and 10R Herva, S Korhonen, K Haapala, et al.
Duodecim; Laaketieteellinen Aikakauskirja|January 1, 1984
[Selective management of fetal hydrocephalus]P Kirkinen, W Serlo, P Jouppila, et al.
American Journal of Medical Genetics|January 1, 1979
Inherited interstitial del(Xp) with minimal clinical consequences: with a note on the location of genes controlling phenotypic featuresR Herva, B Kaluzewski, A de la Chapelle
Journal of Molecular Medicine (Berlin, Germany)|November 21, 2001
A novel mitochondrial DNA mutation and a mutation in the Notch3 gene in a patient with myopathy and CADASILS Finnilä, S Tuisku, R Herva, et al.
Obstetrics and Gynecology|April 1, 1984
Correlation of human chorionic gonadotropin secretion in early pregnancy failure with size of gestational sac and placental histologyP Jouppila, I Huhtaniemi, R Herva, et al.
Prenatal Diagnosis|July 1, 1983
Prenatal detection of hydrolethalus syndromeA L Hartikainen-Sorri, P Kirkinen, R Herva
American Journal of Medical Genetics|March 1, 1985
A lethal autosomal recessive syndrome of multiple congenital contracturesR Herva, J Leisti, P Kirkinen, et al.
Journal of Clinical Ultrasound : JCU|November 1, 1983
Prenatal diagnosis of pleural effusions by ultrasoundP Jouppila, P Kirkinen, R Herva, et al.
European Journal of Obstetrics, Gynecology, and Reproductive Biology|December 1, 1988
Two cases of large placental chorioangioma with fetal and neonatal complicationsE M Nuutinen, U Puistola, R Herva, et al.
The Histochemical Journal|December 1, 1995
Immunohistochemical demonstration of human carbonic anhydrase isoenzyme II in brain tumoursA K Parkkila, R Herva, S Parkkila, et al.
Pageof 11

Showing results (41-50 of 106) with videos related to

Sort By:
Pageof 11
Clinical Genetics|July 1, 1983
Trisomy 10p produced by recombination involving complex paternal translocation between chromosomes 1 and 10R Herva, S Korhonen, K Haapala, et al.
Duodecim; Laaketieteellinen Aikakauskirja|January 1, 1984
[Selective management of fetal hydrocephalus]P Kirkinen, W Serlo, P Jouppila, et al.
American Journal of Medical Genetics|January 1, 1979
Inherited interstitial del(Xp) with minimal clinical consequences: with a note on the location of genes controlling phenotypic featuresR Herva, B Kaluzewski, A de la Chapelle
Journal of Molecular Medicine (Berlin, Germany)|November 21, 2001
A novel mitochondrial DNA mutation and a mutation in the Notch3 gene in a patient with myopathy and CADASILS Finnilä, S Tuisku, R Herva, et al.
Obstetrics and Gynecology|April 1, 1984
Correlation of human chorionic gonadotropin secretion in early pregnancy failure with size of gestational sac and placental histologyP Jouppila, I Huhtaniemi, R Herva, et al.
Prenatal Diagnosis|July 1, 1983
Prenatal detection of hydrolethalus syndromeA L Hartikainen-Sorri, P Kirkinen, R Herva
American Journal of Medical Genetics|March 1, 1985
A lethal autosomal recessive syndrome of multiple congenital contracturesR Herva, J Leisti, P Kirkinen, et al.
Journal of Clinical Ultrasound : JCU|November 1, 1983
Prenatal diagnosis of pleural effusions by ultrasoundP Jouppila, P Kirkinen, R Herva, et al.
European Journal of Obstetrics, Gynecology, and Reproductive Biology|December 1, 1988
Two cases of large placental chorioangioma with fetal and neonatal complicationsE M Nuutinen, U Puistola, R Herva, et al.
The Histochemical Journal|December 1, 1995
Immunohistochemical demonstration of human carbonic anhydrase isoenzyme II in brain tumoursA K Parkkila, R Herva, S Parkkila, et al.
Pageof 11