(Q34387473)

English

Assignment of the locus for congenital lactase deficiency to 2q21, in the vicinity of but separate from the lactase-phlorizin hydrolase gene

scientific article

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scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

1 August 2017

Assignment of the locus for congenital lactase deficiency to 2q21, in the vicinity of but separate from the lactase-phlorizin hydrolase gene (English)

1 reference

Europe PubMed Central

PubMed publication ID

1 August 2017

congenital disorder

0 references

author name string

Järvelä I

1

1 reference

Europe PubMed Central

PubMed publication ID

1 August 2017

Enattah NS

2

1 reference

Europe PubMed Central

PubMed publication ID

1 August 2017

Kokkonen J

3

1 reference

Europe PubMed Central

PubMed publication ID

1 August 2017

Varilo T

4

1 reference

Europe PubMed Central

PubMed publication ID

1 August 2017

Savilahti E

5

1 reference

Europe PubMed Central

PubMed publication ID

1 August 2017

Peltonen L

6

1 reference

Europe PubMed Central

PubMed publication ID

1 August 2017

language of work or name

0 references

publication date

1 October 1998

1 reference

Europe PubMed Central

PubMed publication ID

1 August 2017

American Journal of Human Genetics

1 reference

Europe PubMed Central

PubMed publication ID

1 August 2017

63

1 reference

Europe PubMed Central

PubMed publication ID

1 August 2017

4

1 reference

Europe PubMed Central

PubMed publication ID

1 August 2017

1078-1085

1 reference

Europe PubMed Central

PubMed publication ID

1 August 2017

Defective lactose absorption causing malnutrition in infancy

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1377496

6 July 2018

Tracing an ancestral mutation: genealogical and haplotype analysis of the infantile onset spinocerebellar ataxia locus

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1377496

6 July 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1377496

6 July 2018

A comprehensive genetic map of the human genome based on 5,264 microsatellites

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1377496

6 July 2018

Regional localization of the lactase-phlorizin hydrolase gene, LCT, to chromosome 2q21.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1377496

6 July 2018

A new bacteriophage P1-derived vector for the propagation of large human DNA fragments

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1377496

6 July 2018

A powerful likelihood method for the analysis of linkage disequilibrium between trait loci and one or more polymorphic marker loci

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1377496

6 July 2018

A YAC contig map of the human genome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1377496

6 July 2018

Congenital lactase deficiency. A clinical study on 16 patients

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1377496

6 July 2018

Strategies for multilocus linkage analysis in humans

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1377496

6 July 2018

Blot hybridisation analysis of genomic DNA

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1377496

6 July 2018

The Finnish population structure A genetic and genealogical study

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1377496

6 July 2018

Hereditary diseases in Finland; rare flora in rare soul

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1377496

6 July 2018

Complete primary structure of human and rabbit lactase-phlorizin hydrolase: implications for biosynthesis, membrane anchoring and evolution of the enzyme

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1377496

6 July 2018

Radiation hybrid mapping: a somatic cell genetic method for constructing high-resolution maps of mammalian chromosomes

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1377496

6 July 2018

Structure of the chromosomal gene and cDNAs coding for lactase-phlorizin hydrolase in humans with adult-type hypolactasia or persistence of lactase

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1377496

6 July 2018

Statistical methods for multipoint radiation hybrid mapping

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1377496

6 July 2018

Likelihood ratio tests for linkage and linkage disequilibrium: asymptotic distribution and power.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1377496

27 October 2018

Rare disease genes--lessons and challenges

1 reference

https://pubmed.ncbi.nlm.nih.gov/9758622

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Infantile onset spinocerebellar ataxia represents an allelic disease distinct from other hereditary ataxias

1 reference

https://pubmed.ncbi.nlm.nih.gov/9758622

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Lactose malabsorption in Finnish children of school age

1 reference

https://pubmed.ncbi.nlm.nih.gov/9758622

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The human lactase-phlorizin hydrolase gene is located on chromosome 2

1 reference

https://pubmed.ncbi.nlm.nih.gov/9758622

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

1 reference

Europe PubMed Central

PubMed publication ID

1 August 2017

PMC publication ID

1 reference

Europe PubMed Central

PubMed publication ID

1 August 2017

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

1 August 2017

ResearchGate publication ID

0 references

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