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Clinical Genetics
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July 1, 1983
Trisomy 10p produced by recombination involving complex paternal translocation between chromosomes 1 and 10
R 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 features
R 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 CADASIL
S 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 histology
P Jouppila, I Huhtaniemi, R Herva, et al.
Prenatal Diagnosis
|
July 1, 1983
Prenatal detection of hydrolethalus syndrome
A L Hartikainen-Sorri, P Kirkinen, R Herva
American Journal of Medical Genetics
|
March 1, 1985
A lethal autosomal recessive syndrome of multiple congenital contractures
R Herva, J Leisti, P Kirkinen, et al.
Journal of Clinical Ultrasound : JCU
|
November 1, 1983
Prenatal diagnosis of pleural effusions by ultrasound
P 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 complications
E M Nuutinen, U Puistola, R Herva, et al.
The Histochemical Journal
|
December 1, 1995
Immunohistochemical demonstration of human carbonic anhydrase isoenzyme II in brain tumours
A K Parkkila, R Herva, S Parkkila, et al.
Page
of 11
Search research articles
Search
Showing results (41-50 of 106) with videos related to
Sort By:
Page
of 11
Clinical Genetics
|
July 1, 1983
Trisomy 10p produced by recombination involving complex paternal translocation between chromosomes 1 and 10
R 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 features
R 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 CADASIL
S 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 histology
P Jouppila, I Huhtaniemi, R Herva, et al.
Prenatal Diagnosis
|
July 1, 1983
Prenatal detection of hydrolethalus syndrome
A L Hartikainen-Sorri, P Kirkinen, R Herva
American Journal of Medical Genetics
|
March 1, 1985
A lethal autosomal recessive syndrome of multiple congenital contractures
R Herva, J Leisti, P Kirkinen, et al.
Journal of Clinical Ultrasound : JCU
|
November 1, 1983
Prenatal diagnosis of pleural effusions by ultrasound
P 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 complications
E M Nuutinen, U Puistola, R Herva, et al.
The Histochemical Journal
|
December 1, 1995
Immunohistochemical demonstration of human carbonic anhydrase isoenzyme II in brain tumours
A K Parkkila, R Herva, S Parkkila, et al.
Page
of 11