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P Nokelainen

Showing results (11-20 of 17) with videos related to

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American Journal of Medical Genetics|December 18, 2001
Two brothers with macrocephaly, progressive cerebral atrophy and abnormal white matter, severe mental retardation, and Lennox-Gastaut spectrum type epilepsy: an inherited encephalopathy of childhood?P Nokelainen, H Heiskala, R Raininko, et al.
Endocrinology|October 1, 1994
Rat 17 beta-hydroxysteroid dehydrogenase type 1: primary structure and regulation of enzyme expression in rat ovary by diethylstilbestrol and gonadotropins in vivoS Ghersevich, P Nokelainen, M Poutanen, et al.
Forensic Science International|September 16, 1994
A microsatellite polymorphism in the von Willebrand factor gene: comparison of allele frequencies in different population samples and evaluation for forensic medicineA Sajantila, P Pacek, M Lukka, et al.
Journal of Medical Genetics|November 1, 1992
Comparison of the myotonic dystrophy associated CTG repeat in European and Japanese populationsJ Davies, H Yamagata, P Shelbourne, et al.
Human Genetics|October 1, 1990
Linkage disequilibrium detected between dystrophia myotonica and APOC2 locus in the Finnish populationP Nokelainen, L Alanen-Kurki, R Winqvist, et al.
Nature Genetics|February 1, 1994
Meiotic drive at the myotonic dystrophy locus?N Carey, K Johnson, P Nokelainen, et al.
Clinical Genetics|April 1, 1993
The DM mutation; diagnostic applications in the Finnish populationP Nokelainen, P Shelbourne, D Shaw, et al.
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Showing results (11-20 of 17) with videos related to

Sort By:
Pageof 2
You have reached the last page of results.This site can display upto 17 results.
American Journal of Medical Genetics|December 18, 2001
Two brothers with macrocephaly, progressive cerebral atrophy and abnormal white matter, severe mental retardation, and Lennox-Gastaut spectrum type epilepsy: an inherited encephalopathy of childhood?P Nokelainen, H Heiskala, R Raininko, et al.
Endocrinology|October 1, 1994
Rat 17 beta-hydroxysteroid dehydrogenase type 1: primary structure and regulation of enzyme expression in rat ovary by diethylstilbestrol and gonadotropins in vivoS Ghersevich, P Nokelainen, M Poutanen, et al.
Forensic Science International|September 16, 1994
A microsatellite polymorphism in the von Willebrand factor gene: comparison of allele frequencies in different population samples and evaluation for forensic medicineA Sajantila, P Pacek, M Lukka, et al.
Journal of Medical Genetics|November 1, 1992
Comparison of the myotonic dystrophy associated CTG repeat in European and Japanese populationsJ Davies, H Yamagata, P Shelbourne, et al.
Human Genetics|October 1, 1990
Linkage disequilibrium detected between dystrophia myotonica and APOC2 locus in the Finnish populationP Nokelainen, L Alanen-Kurki, R Winqvist, et al.
Nature Genetics|February 1, 1994
Meiotic drive at the myotonic dystrophy locus?N Carey, K Johnson, P Nokelainen, et al.
Clinical Genetics|April 1, 1993
The DM mutation; diagnostic applications in the Finnish populationP Nokelainen, P Shelbourne, D Shaw, et al.
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