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American Journal of Medical Genetics
|
January 1, 1980
Dicentric Y chromosome arising via tandem translocation
R Herva, I Saarinen, H Savikurki, et al.
Human Genetics
|
January 1, 1981
A deletion in chromosome 22 can cause DiGeorge syndrome
A de la Chapelle, R Herva, M Koivisto, et al.
Neurology
|
May 1, 1993
Adult-onset diabetes mellitus and neurosensory hearing loss in maternal relatives of MELAS patients in a family with the tRNA(Leu(UUR)) mutation
A M Remes, K Majamaa, R Herva, et al.
Brain Pathology (Zurich, Switzerland)
|
April 14, 2000
Northern epilepsy: a novel form of neuronal ceroid-lipofuscinosis
R Herva, J Tyynelä, A Hirvasniemi, et al.
American Journal of Medical Genetics
|
January 1, 1988
A syndrome of multiple congenital contractures: neuropathological analysis on five fetal cases
R Herva, N G Conradi, H Kalimo, et al.
Journal of Neuro-Oncology
|
July 15, 2000
Matrix metalloproteinase 2 (MMP-2) immunoreactive protein is associated with poor grade and survival in brain neoplasms
J Jäälinojä, R Herva, M Korpela, et al.
Acta Neuropathologica
|
January 1, 1995
Familial fetal akinesia deformation sequence with a skeletal muscle maturation defect
K Vuopala, F Pedrosa-Domellöf, R Herva, et al.
Bone
|
November 13, 2001
Human macrophage metalloelastase (MMP-12) expression is induced in chondrocytes during fetal development and malignant transformation
E Kerkelä, T Böhling, R Herva, et al.
Acta Histochemica
|
January 1, 1990
Cystatin A and B in the development of human squamous epithelia
H Pernu, O Räsänen, T Salo, et al.
Placenta
|
April 27, 2005
Expression of 3beta-hydroxysteroid dehydrogenase type 1, P450 aromatase, and 17beta-hydroxysteroid dehydrogenase types 1, 2, 5 and 7 mRNAs in human early and mid-gestation placentas
Y Li, V Isomaa, A Pulkka, et al.
Page
of 11
Search research articles
Search
Showing results (61-70 of 106) with videos related to
Sort By:
Page
of 11
American Journal of Medical Genetics
|
January 1, 1980
Dicentric Y chromosome arising via tandem translocation
R Herva, I Saarinen, H Savikurki, et al.
Human Genetics
|
January 1, 1981
A deletion in chromosome 22 can cause DiGeorge syndrome
A de la Chapelle, R Herva, M Koivisto, et al.
Neurology
|
May 1, 1993
Adult-onset diabetes mellitus and neurosensory hearing loss in maternal relatives of MELAS patients in a family with the tRNA(Leu(UUR)) mutation
A M Remes, K Majamaa, R Herva, et al.
Brain Pathology (Zurich, Switzerland)
|
April 14, 2000
Northern epilepsy: a novel form of neuronal ceroid-lipofuscinosis
R Herva, J Tyynelä, A Hirvasniemi, et al.
American Journal of Medical Genetics
|
January 1, 1988
A syndrome of multiple congenital contractures: neuropathological analysis on five fetal cases
R Herva, N G Conradi, H Kalimo, et al.
Journal of Neuro-Oncology
|
July 15, 2000
Matrix metalloproteinase 2 (MMP-2) immunoreactive protein is associated with poor grade and survival in brain neoplasms
J Jäälinojä, R Herva, M Korpela, et al.
Acta Neuropathologica
|
January 1, 1995
Familial fetal akinesia deformation sequence with a skeletal muscle maturation defect
K Vuopala, F Pedrosa-Domellöf, R Herva, et al.
Bone
|
November 13, 2001
Human macrophage metalloelastase (MMP-12) expression is induced in chondrocytes during fetal development and malignant transformation
E Kerkelä, T Böhling, R Herva, et al.
Acta Histochemica
|
January 1, 1990
Cystatin A and B in the development of human squamous epithelia
H Pernu, O Räsänen, T Salo, et al.
Placenta
|
April 27, 2005
Expression of 3beta-hydroxysteroid dehydrogenase type 1, P450 aromatase, and 17beta-hydroxysteroid dehydrogenase types 1, 2, 5 and 7 mRNAs in human early and mid-gestation placentas
Y Li, V Isomaa, A Pulkka, et al.
Page
of 11