(Q34531986)

2 August 2017

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title

Finnish Disease Heritage I: characteristics, causes, background (English)

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2 August 2017

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Reijo Norio

1

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2 August 2017

publication date

8 March 2003

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2 August 2017

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2 August 2017

volume

112

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2 August 2017

issue

5-6

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2 August 2017

page(s)

441-456

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https://scigraph.springernature.com/pub.10.1007/s00439-002-0875-3

2 August 2017

exact match

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cites work

Hereditary diseases in Finland--from the clinician's and scientist's point of view

1 reference

12 December 2020

Association of parental consanguinity with decreased birth weight and increased rate of early death and congenital malformations

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12 December 2020

Proteinuria and prenatal diagnosis of congenital nephrosis in fetal carriers of nephrin gene mutations

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12 December 2020

Age and origin of two common MLH1 mutations predisposing to hereditary colon cancer

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12 December 2020

Linkage disequilibrium mapping in isolated populations: the example of Finland revisited

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12 December 2020

Inbreeding in Finland

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12 December 2020

The occurrence of consanguineous marriages in Hungary

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12 December 2020

Refined mapping of the Cohen syndrome gene by linkage disequilibrium.

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12 December 2020

Linkage disequilibrium mapping in isolated founder populations: diastrophic dysplasia in Finland

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12 December 2020

Differential Systematics

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12 December 2020

The heredity of congential nephrosis

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12 December 2020

Familial hypercholesterolaemia in Finland: common, rare and mild mutations of the LDL receptor and their clinical consequences. Finnish FH-group

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12 December 2020

Homozygosity mapping: a way to map human recessive traits with the DNA of inbred children

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12 December 2020

Heredity in the congenital nephrotic syndrome. A genetic study of 57 finnish FAMILIES WITH A REVIEW OF REPORTED CASES

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12 December 2020

Localization of the EPM1 gene for progressive myoclonus epilepsy on chromosome 21: linkage disequilibrium allows high resolution mapping

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12 December 2020

Hereditary diseases in Finland; rare flora in rare soul

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12 December 2020

Autosomal recessive disorders in Saguenay-Lac-Saint-Jean (Quebec, Canada): a study of inbreeding

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12 December 2020

Role of nephrin in cell junction formation in human nephrogenesis

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12 December 2020

Unstable minisatellite expansion causing recessively inherited myoclonus epilepsy, EPM1

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12 December 2020

Multiple founder effects and geographical clustering of BRCA1 and BRCA2 families in Finland

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12 December 2020

Genetic control of serum IgE levels and asthma: linkage and linkage disequilibrium studies in an isolated population.

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12 December 2020

Interaction of genetic and environmental factors in the pathogenesis of insulin-dependent diabetes mellitus

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12 December 2020

Mutations of Bacteria from Virus Sensitivity to Virus Resistance

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12 December 2020

Increasing incidence of childhood-onset type I diabetes in 3 Baltic countries and Finland 1983-1998.

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12 December 2020

Northern epilepsy syndrome: an inherited childhood onset epilepsy with associated mental deterioration

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12 December 2020

Dissecting a population genome for targeted screening of disease mutations

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12 December 2020

Molecular genetics of the Finnish disease heritage.

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12 December 2020

Random search for shared chromosomal regions in four affected individuals: the assignment of a new hereditary ataxia locus

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12 December 2020

Inbreeding in recessive diseases

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12 December 2020

The Finnish population structure A genetic and genealogical study

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12 December 2020

Linkage disequilibrium in isolated populations: Finland and a young sub-population of Kuusamo.

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12 December 2020

Is the Finnish heritage of disease disappearing?

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12 December 2020

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12 December 2020

The age of human mutation: genealogical and linkage disequilibrium analysis of the CLN5 mutation in the Finnish population.

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12 December 2020

Dissecting the epidemiology of a trinucleotide repeat disease - example of FRDA in Finland

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12 December 2020

10.1007/S00439-002-0875-3

Identifiers

DOI

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Dimensions Publication ID

1075249510

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1 reference