Detalhe da pesquisa
1.
Evaluation of the ARKRAY AUTION Eleven reflectometer in detecting microalbuminuria with AUTION Screen test strips and proteinuria with AUTION Sticks 10PA strips.
Scand J Clin Lab Invest
; 69(1): 52-64, 2009.
Artigo
em Inglês
| MEDLINE | ID: mdl-18923968
2.
Meiotic drive at the myotonic dystrophy locus?
Nat Genet
; 6(2): 117-8, 1994 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-8162064
3.
Expression cloning of a novel estrogenic mouse 17 beta-hydroxysteroid dehydrogenase/17-ketosteroid reductase (m17HSD7), previously described as a prolactin receptor-associated protein (PRAP) in rat.
Mol Endocrinol
; 12(7): 1048-59, 1998 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-9658408
4.
Expression of mouse 17beta-hydroxysteroid dehydrogenase/17-ketosteroid reductase type 7 in the ovary, uterus, and placenta: localization from implantation to late pregnancy.
Endocrinology
; 141(2): 772-8, 2000 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-10650959
5.
Rat 17 beta-hydroxysteroid dehydrogenase type 1: primary structure and regulation of enzyme expression in rat ovary by diethylstilbestrol and gonadotropins in vivo.
Endocrinology
; 135(4): 1477-87, 1994 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-7925110
6.
A patient with 2 different repeat expansion mutations.
Arch Neurol
; 57(8): 1199-203, 2000 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-10927802
7.
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?
Am J Med Genet
; 103(3): 198-206, 2001 Oct 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-11745991
8.
Two 17beta-hydroxysteroid dehydrogenases (17HSDs) of estradiol biosynthesis: 17HSD type 1 and type 7.
J Steroid Biochem Mol Biol
; 69(1-6): 431-9, 1999.
Artigo
em Inglês
| MEDLINE | ID: mdl-10419022
9.
Nonvacuolar myopathy in a large family with both late adult onset distal myopathy and severe proximal muscular dystrophy.
J Neurol Sci
; 113(2): 214-21, 1992 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-1487757
10.
A microsatellite polymorphism in the von Willebrand factor gene: comparison of allele frequencies in different population samples and evaluation for forensic medicine.
Forensic Sci Int
; 68(2): 91-102, 1994 Sep 16.
Artigo
em Inglês
| MEDLINE | ID: mdl-7988968
11.
Genetic effects on human cognition: lessons from the study of mental retardation syndromes.
J Neurol Neurosurg Psychiatry
; 72(3): 287-96, 2002 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-11861682
12.
Linkage analyses in tibial muscular dystrophy.
Hum Hered
; 46(2): 98-107, 1996.
Artigo
em Inglês
| MEDLINE | ID: mdl-8666419
13.
Molecular cloning of mouse 17 beta-hydroxysteroid dehydrogenase type 1 and characterization of enzyme activity.
Eur J Biochem
; 236(2): 482-90, 1996 Mar 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-8612620
14.
Usefulness of chromosome 19 RFLP haplotypes in the diagnosis of myotonic dystrophy.
Muscle Nerve
; 14(5): 451-6, 1991 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-1678492
15.
The DM mutation; diagnostic applications in the Finnish population.
Clin Genet
; 43(4): 190-5, 1993 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-8101149
16.
Comparison of the myotonic dystrophy associated CTG repeat in European and Japanese populations.
J Med Genet
; 29(11): 766-9, 1992 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-1453423
17.
Linkage disequilibrium detected between dystrophia myotonica and APOC2 locus in the Finnish population.
Hum Genet
; 85(5): 541-5, 1990 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-1977684