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Genomics
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April 1, 1993
Kearns-Sayre syndrome case presenting a mitochondrial DNA deletion with unusual direct repeats and a rudimentary RNAase mitochondrial ribonucleotide processing target sequence
A M Remes, K J Peuhkurinen, R Herva, et al.
Journal of Medical Genetics
|
January 1, 1995
Lethal congenital contracture syndrome (LCCS), a fetal anterior horn cell disease, is not linked to the SMA 5q locus
K Vuopala, P Mäkelä-Bengs, A Suomalainen, et al.
American Journal of Respiratory Cell and Molecular Biology
|
October 6, 2001
Distribution and mRNA expression of tenascin-C in developing human lung
R Kaarteenaho-Wiik, V Kinnula, R Herva, et al.
Clinical and Experimental Immunology
|
July 1, 1981
Immunodeficiency associated with a deletion in the short arm of the X-chromosome
T Nurmi, M Uhari, S L Linna, et al.
Developmental Medicine and Child Neurology
|
June 30, 2000
Human herpesvirus-6 associated encephalitis with subsequent infantile spasms and cerebellar astrocytoma
H Rantala, L Mannonen, S Ahtiluoto, et al.
Annals of Medicine
|
April 1, 1990
Prenatal diagnosis of single gene disorders in northern Finland
J Leisti, P Jouppila, A Mustonen, et al.
Clinical Genetics
|
March 1, 1985
The incidence of Down syndrome in northern Finland with special reference to maternal age
J Leisti, L Vahtola, S L Linna, et al.
APMIS : Acta Pathologica, Microbiologica, Et Immunologica Scandinavica
|
October 1, 1994
p53 immunohistochemical positivity as a prognostic marker in intracranial tumours
Y Soini, A Niemelä, D Kamel, et al.
Neurology
|
July 28, 2004
Hereditary dementia with intracerebral hemorrhages and cerebral amyloid angiopathy
A M Remes, S Finnilä, H Mononen, et al.
Epilepsia
|
March 1, 1995
Carbamazepine and its metabolites in human perfused placenta and in maternal and cord blood
P Pienimäki, A L Hartikainen, P Arvela, et al.
Page
of 11
Search research articles
Search
Showing results (71-80 of 106) with videos related to
Sort By:
Page
of 11
Genomics
|
April 1, 1993
Kearns-Sayre syndrome case presenting a mitochondrial DNA deletion with unusual direct repeats and a rudimentary RNAase mitochondrial ribonucleotide processing target sequence
A M Remes, K J Peuhkurinen, R Herva, et al.
Journal of Medical Genetics
|
January 1, 1995
Lethal congenital contracture syndrome (LCCS), a fetal anterior horn cell disease, is not linked to the SMA 5q locus
K Vuopala, P Mäkelä-Bengs, A Suomalainen, et al.
American Journal of Respiratory Cell and Molecular Biology
|
October 6, 2001
Distribution and mRNA expression of tenascin-C in developing human lung
R Kaarteenaho-Wiik, V Kinnula, R Herva, et al.
Clinical and Experimental Immunology
|
July 1, 1981
Immunodeficiency associated with a deletion in the short arm of the X-chromosome
T Nurmi, M Uhari, S L Linna, et al.
Developmental Medicine and Child Neurology
|
June 30, 2000
Human herpesvirus-6 associated encephalitis with subsequent infantile spasms and cerebellar astrocytoma
H Rantala, L Mannonen, S Ahtiluoto, et al.
Annals of Medicine
|
April 1, 1990
Prenatal diagnosis of single gene disorders in northern Finland
J Leisti, P Jouppila, A Mustonen, et al.
Clinical Genetics
|
March 1, 1985
The incidence of Down syndrome in northern Finland with special reference to maternal age
J Leisti, L Vahtola, S L Linna, et al.
APMIS : Acta Pathologica, Microbiologica, Et Immunologica Scandinavica
|
October 1, 1994
p53 immunohistochemical positivity as a prognostic marker in intracranial tumours
Y Soini, A Niemelä, D Kamel, et al.
Neurology
|
July 28, 2004
Hereditary dementia with intracerebral hemorrhages and cerebral amyloid angiopathy
A M Remes, S Finnilä, H Mononen, et al.
Epilepsia
|
March 1, 1995
Carbamazepine and its metabolites in human perfused placenta and in maternal and cord blood
P Pienimäki, A L Hartikainen, P Arvela, et al.
Page
of 11