Linkage analysis in Marfan syndrome. - Wikidata - wikimedia - TriplyDB

Linkage analysis in Marfan syndrome.

Linkage analysis in Marfan syndrome.

http://www.wikidata.org/entity/Q33597166

about

An exclusion map of Marfan syndrome Marfan syndrome: defective synthesis, secretion, and extracellular matrix formation of fibrillin by cultured dermal fibroblasts.Marfan syndrome is closely linked to a marker on chromosome 15q1.5----q2.1.

P2860

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P2860

Linkage analysis in Marfan syndrome.

http://www.wikidata.org/entity/Q33597166

description

1990 nî lūn-bûn

@nan

1990 թուականի Փետրուարին հրատարակուած գիտական յօդուած

@hyw

1990 թվականի փետրվարին հրատարակված գիտական հոդված

@hy

1990年の論文

@ja

1990年論文

@yue

1990年論文

@zh-hant

1990年論文

@zh-hk

1990年論文

@zh-mo

1990年論文

@zh-tw

1990年论文

@wuu

name

Linkage analysis in Marfan syndrome.

@ast

Linkage analysis in Marfan syndrome.

@en

type

label

Linkage analysis in Marfan syndrome.

@ast

Linkage analysis in Marfan syndrome.

@en

prefLabel

Linkage analysis in Marfan syndrome.

@ast

Linkage analysis in Marfan syndrome.

@en

P1433

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P1433

Journal of Medical Genetics

P1476

Linkage analysis in Marfan syndrome.

@en

P2093

C A Hyde

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

L Hudgins

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

M Sarfarazi

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

P Tsipouras

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

R C Schwartz

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

S H Blanton

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T R Sottile

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P2860

Polymorphic human glucose transporter gene (GLUT) is on chromosome 1p31.3----p35

Strategies for multilocus linkage analysis in humans

Exclusion of the alpha 1(II) collagen structural gene as the mutant locus in type II Ehlers-Danlos syndrome.

Exclusion of the alpha 2(I) and alpha 1(III) collagen genes as the mutant loci in a Marfan syndrome family.

Variable number of tandem repeat (VNTR) markers for human gene mapping.

Estimating the power of a proposed linkage study: a practical computer simulation approach.

Segregation of all four major fibrillar collagen genes in the Marfan syndrome.

Isolation and subregional mapping of an arbitrary cloned probe detecting a common RFLP on human chromosome 2.

A genetic linkage map of 27 loci from PND to FY on the short arm of human chromosome I.

Estimation of the recombination fraction in human pedigrees: efficient computation of the likelihood for human linkage studies.

P304

86-90

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scholarly article

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10.1136/JMG.27.2.86

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2

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27

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1990-02-01T00:00:00Z

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21185497

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1969490

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P932

1016926

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