Homozygosity mapping at Alström syndrome to chromosome 2p - Wikidata - wikimedia - TriplyDB

Homozygosity mapping at Alström syndrome to chromosome 2p

Homozygosity mapping at Alström syndrome to chromosome 2p

http://www.wikidata.org/entity/Q28305514

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Cloning, expression, and genetic mapping of Sema W, a member of the semaphorin family New criteria for improved diagnosis of Bardet-Biedl syndrome: results of a population survey APOA5 Q97X mutation identified through homozygosity mapping causes severe hypertriglyceridemia in a Chilean consanguineous family.Genetics of Type 2 diabetes.Genetic isolates in ophthalmic diseases.Perspectives in Pediatric Pathology, Chapter 21. Testicular Pathology in Heritable Metabolic Disease.Genealogy, natural history, and phenotype of Alström syndrome in a large Acadian kindred and three additional families.The human obesity gene map: the 1997 update.Early-onset liver disease complicated with acute liver failure in Alstrom syndrome.Effect of metformin and rosiglitazone in a prepubertal boy with Alström syndrome.Ophthalmic features of cone-rod dystrophy caused by pathogenic variants in the ALMS1 gene.Obesity genetics: insights from the Pakistani population.Alström's syndrome with Kleinfelter's karyotype.TGFA: exon-intron structure and evaluation as a candidate gene for Alström syndrome.

P2860

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P2860

Homozygosity mapping at Alström syndrome to chromosome 2p

http://www.wikidata.org/entity/Q28305514

description

1997 nî lūn-bûn

@nan

1997 թուականի Փետրուարին հրատարակուած գիտական յօդուած

@hyw

1997 թվականի փետրվարին հրատարակված գիտական հոդված

@hy

1997年の論文

@ja

1997年論文

@yue

1997年論文

@zh-hant

1997年論文

@zh-hk

1997年論文

@zh-mo

1997年論文

@zh-tw

1997年论文

@wuu

name

Homozygosity mapping at Alström syndrome to chromosome 2p

@ast

Homozygosity mapping at Alström syndrome to chromosome 2p

@en

Homozygosity mapping at Alström syndrome to chromosome 2p

@nl

type

label

Homozygosity mapping at Alström syndrome to chromosome 2p

@ast

Homozygosity mapping at Alström syndrome to chromosome 2p

@en

Homozygosity mapping at Alström syndrome to chromosome 2p

@nl

prefLabel

Homozygosity mapping at Alström syndrome to chromosome 2p

@ast

Homozygosity mapping at Alström syndrome to chromosome 2p

@en

Homozygosity mapping at Alström syndrome to chromosome 2p

@nl

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P1433

Human Molecular Genetics

P1476

Homozygosity mapping at Alström syndrome to chromosome 2p

@en

P2093

G B Collin

http://www.w3.org/2001/XMLSchema#string

J D Marshall

http://www.w3.org/2001/XMLSchema#string

L R Cardon

http://www.w3.org/2001/XMLSchema#string

P M Nishina

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P2860

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

Chromosomal mapping of the human annexin IV (ANX4) gene

Identity-by-descent and association mapping of a recessive gene for Hirschsprung disease on human chromosome 13q22

Identification of a Bardet-Biedl syndrome locus on chromosome 3 and evaluation of an efficient approach to homozygosity mapping

Chromosomal localization of the beta-adducin gene to mouse chromosome 6 and human chromosome 2

Physical mapping of the human glutamine:fructose-6-phosphate amidotransferase gene (GFPT) to chromosome 2p13

Use of a DNA pooling strategy to identify a human obesity syndrome locus on chromosome 15

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

The gene for human transforming growth factor alpha is on the short arm of chromosome 2.

Linkage of Bardet-Biedl syndrome to chromosome 16q and evidence for non-allelic genetic heterogeneity.

P304

213-9

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scholarly article

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10.1093/HMG/6.2.213

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2

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6

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1997-02-01T00:00:00Z

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14147816

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9063741

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