Found: 31
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A new simple and rapid dual assay for AFP and free β hCG in screening for Down syndrome.
- Published in:
- Clinical Genetics, 1994, v. 45, n. 1, p. 1, doi. 10.1111/j.1399-0004.1994.tb03980.x
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- Publication type:
- Article
Sex hormones, inflammation and the metabolic syndrome: a population-based study.
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- European Journal of Endocrinology, 2003, v. 149, n. 6, p. 0601
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- Publication type:
- Article
Periderm prevents pathological epithelial adhesions during embryogenesis.
- Published in:
- Journal of Clinical Investigation, 2014, v. 124, n. 9, p. 3891, doi. 10.1172/JCI71946
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- Publication type:
- Article
MKS1, encoding a component of the flagellar apparatus basal body proteome, is mutated in Meckel syndrome.
- Published in:
- Nature Genetics, 2006, v. 38, n. 2, p. 155, doi. 10.1038/ng1714
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- Article
Prenatally detected trisomy 7 mosaicism in a dysmorphic child.
- Published in:
- Prenatal Diagnosis, 2002, v. 22, n. 7, p. 541, doi. 10.1002/pd.348
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- Article
Maternal midtrimester serum AFP and free β-hCG levels in in vitro fertilization twin pregnancies.
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- Prenatal Diagnosis, 2000, v. 20, n. 3, p. 221, doi. 10.1002/(SICI)1097-0223(200003)20:3<221::AID-PD787>3.0.CO;2-S
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- Article
DNA-based prenatal diagnosis of the infantile form of neuronal ceroid lipofuscinosis (INCL, CLN1).
- Published in:
- 1991
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- Publication type:
- journal article
Prenatal diagnosis of the infantile type of neuronal ceroid lipofuscinosis by electron microscopic investigation of human chorionic villi.
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- 1990
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- Publication type:
- journal article
Trisomy 12 mosaicism in amniocytes and dysmorphic child despite normal chromosomes in fetal blood sample.
- Published in:
- Prenatal Diagnosis, 1989, v. 9, n. 6, p. 433, doi. 10.1002/pd.1970090609
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- Publication type:
- Article
Amniotic fluid pregnancy-specific β1-glycoprotein (SP1) in fetal developmental disorders.
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- Prenatal Diagnosis, 1984, v. 4, n. 2, p. 147, doi. 10.1002/pd.1970040210
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- Publication type:
- Article
The predictive value of cardiorespiratory fitness for cardiovascular events in men with various risk profiles: a prospective population-based cohort study.
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- European Heart Journal, 2004, v. 25, n. 16, p. 1428, doi. 10.1016/j.ehj.2004.06.013
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- Publication type:
- Article
Cardiorespiratory Fitness and the Progression of Carotid Atherosclerosis in Middle-Aged Men.
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- Annals of Internal Medicine, 2001, v. 134, n. 1, p. 12, doi. 10.7326/0003-4819-134-1-200101020-00008
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- Publication type:
- Article
Two-stage ultrasonography in screening for fetal anomalies at 13-14 and 18-22 weeks of gestation.
- Published in:
- 2004
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- Publication type:
- journal article
Associations of total testosterone and sex hormone-binding globulin levels with insulin sensitivity in middle-aged Finnish men.
- Published in:
- Diabetes Care, 2007, v. 30, n. 4, p. e13, doi. 10.2337/dc06-1979
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- Publication type:
- Article
Testosterone and Sex Hormone-Binding Globulin Predict the Metabolic Syndrome and Diabetes in Middle-Aged Men.
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- Diabetes Care, 2004, v. 27, n. 5, p. 1036, doi. 10.2337/diacare.27.5.1036
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- Publication type:
- Article
Reduced IGFBP-1 is associated with thickening of the carotid wall in type 2 diabetes.
- Published in:
- 2002
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- Publication type:
- journal article
Ultrasonographic manifestations of carotid atherosclerosis and glucose intolerance in elderly eastern Finnish men.
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- 1998
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- Publication type:
- journal article
Body iron stores are associated with serum insulin and blood glucose concentrations. Population study in 1,013 eastern Finnish men.
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- 1997
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- Publication type:
- journal article
Hydrolethalus: a midline malformation syndrome with optic nerve coloboma and hypoplasia.
- Published in:
- Acta Neuropathologica, 1996, v. 91, n. 5, p. 511, doi. 10.1007/s004010050459
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- Publication type:
- Article
Donation of Blood Is Associated with Reduced Risk of Myocardial Infarction.
- Published in:
- American Journal of Epidemiology, 1998, v. 148, n. 5, p. 445, doi. 10.1093/oxfordjournals.aje.a009669
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- Publication type:
- Article
Association between Plasma Fibrinogen Concentration and Five Socioeconomic Indices in the Kuopio Ischemic Heart Disease Risk Factor Study.
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- American Journal of Epidemiology, 1993, v. 137, n. 3, p. 292, doi. 10.1093/oxfordjournals.aje.a116676
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- Article
THE AUTHORS REPLY.
- Published in:
- American Journal of Epidemiology, 1992, v. 135, n. 7, p. 833, doi. 10.1093/oxfordjournals.aje.a116371
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- Article
Serum Copper and the Risk of Acute Myocardial Infarction: A Prospective Population Study in Men in Eastern Finland.
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- American Journal of Epidemiology, 1991, v. 134, n. 3, p. 268, doi. 10.1093/oxfordjournals.aje.a116080
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- Publication type:
- Article
A prospective study of 63 couples with a history of recurrent spontaneous abortion: contributing factors and outcome of subsequent pregnancies.
- Published in:
- 1993
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- Publication type:
- journal article
The genetic aetiology of retinal degeneration in children in Finland – new founder mutations identified.
- Published in:
- Acta Ophthalmologica (1755375X), 2019, v. 97, n. 8, p. 805, doi. 10.1111/aos.14128
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- Publication type:
- Article
Mutation spectrum of Meckel syndrome genes: one group of syndromes or several distinct groups?
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- Human Mutation, 2009, v. 30, n. 8, p. E813, doi. 10.1002/humu.21057
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- Article
Perceived health status and morbidity and mortality: evidence from the Kuopio ischaemic heart disease risk factor study.
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- 1996
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- Publication type:
- journal article
Hydrolethalus syndrome is caused by a missense mutation in a novel gene HYLS1.
- Published in:
- Human Molecular Genetics, 2005, v. 14, n. 11, p. 1475, doi. 10.1093/hmg/ddi157
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- Publication type:
- Article
Does Low Socioeconomic Status Potentiate the Effects of Heightened Cardiovascular Responses to Stress on the Progression of Carotid Atherosclerosis?
- Published in:
- American Journal of Public Health, 1998, v. 88, n. 3, p. 389, doi. 10.2105/AJPH.88.3.389
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- Article
The hydrolethalus syndrome: delineation of a 'new', lethal malformation syndrome based on 28 patients.
- Published in:
- Clinical Genetics, 1981, v. 19, n. 5, p. 321, doi. 10.1111/j.1399-0004.1981.tb00718.x
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- Publication type:
- Article
Improved prenatal diagnosis of the congenital nephrotic syndrome of the Finnish type based on DNA analysis.
- Published in:
- Kidney International, 1997, v. 51, n. 3, p. 868, doi. 10.1111/1523-1755.ep14221311
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- Publication type:
- Article