(Q41866345)

13 October 2017

Linkage relationships of the apolipoprotein C1 gene and a cytochrome P450 gene (CYP2A) to myotonic dystrophy (English)

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13 October 2017

K V Walsh

1

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13 October 2017

H G Harley

2

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13 October 2017

J D Brook

3

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13 October 2017

S A Rundle

4

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13 October 2017

M Sarfarazi

5

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13 October 2017

P S Harper

6

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13 October 2017

D J Shaw

7

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13 October 2017

1 August 1990

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13 October 2017

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13 October 2017

85

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13 October 2017

305-310

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13 October 2017

3

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https://scigraph.springernature.com/pub.10.1007/bf00206751

13 October 2017

0 references

cites work

Close linkage of the human cytochrome P450IIA and P450IIB gene subfamilies: implications for the assignment of substrate specificity

1 reference

12 December 2020

Localization of a human Na+,K+-ATPase alpha subunit gene to chromosome 19q12----q13.2 and linkage to the myotonic dystrophy locus

1 reference

12 December 2020

A chromosome 19 clone from a translocation breakpoint shows close linkage and linkage disequilibrium with myotonic dystrophy

1 reference

12 December 2020

Long-range restriction map of a region of human chromosome 19 containing the apolipoprotein genes, a CLL-associated translocation breakpoint, and two polymorphic MluI sites

1 reference

12 December 2020

Criteria for establishing the validity of genetic recombination in myotonic dystrophy

1 reference

12 December 2020

Chromosomal assignments of genes coding for components of the mixed-function oxidase system in mice. Genetic localization of the cytochrome P-450PCN and P-450PB gene families and the nadph-cytochrome P-450 oxidoreductase and epoxide hydratase genes

1 reference

12 December 2020

Strategies for multilocus linkage analysis in humans

1 reference

12 December 2020

Genetic polymorphisms for a phenobarbital-inducible cytochrome P-450 map to the Coh locus in mice

1 reference

12 December 2020

The locus for apolipoprotein CII is closely linked to the apolipoprotein E locus on chromosome 19 in man

1 reference

12 December 2020

Genetic linkage between the loci for myotonic dystrophy and peptidase D

1 reference

12 December 2020

Characterisation of mRNAs encoding the precursor for human apolipoprotein CI

1 reference

12 December 2020

Regional localization of a human cytochrome P-450 (CYP1) to chromosome 19q13.1-13.3.

1 reference

12 December 2020

The gene for apolipoprotein C-II is closely linked to the gene for apolipo-protein E on chromosome 19

1 reference

12 December 2020

Linkage analysis and family classification under heterogeneity

1 reference

12 December 2020

Definition of subchromosomal intervals around the myotonic dystrophy gene region at 19q

1 reference

12 December 2020

Mapping genetic markers on human chromosome 19 using subchromosomal fragments in somatic cell hybrids

1 reference

12 December 2020

RFLP for a human cytochrome P-450 gene at 19q13.1-qter (HGM8 provisional designation CYPI)

1 reference

12 December 2020

Linkage between the loci for peptidase D and apolipoprotein CII on chromosome 19

1 reference

12 December 2020

There are two gene sequences for human apolipoprotein CI (apo CI) on chromosome 19, one of which is 4 kb from the gene for apo E

1 reference

12 December 2020

The apolipoprotein CII gene: subchromosomal localisation and linkage to the myotonic dystrophy locus

1 reference

12 December 2020

Regional localisations and linkage relationships of seven RFLPs and myotonic dystrophy on chromosome 19

1 reference

12 December 2020

Myotonic dystrophy in Quebec: geographical distribution and concept of genetic homogeneity

1 reference

12 December 2020

Outlook for a clinically normal child in a sibship with congenital myotonic dystrophy

1 reference

12 December 2020

A cytochrome P-450 gene family mapped to human chromosome 19

1 reference

12 December 2020

Regional mapping of human chromosome 19: organization of genes for plasma lipid transport (APOC1, -C2, and -E and LDLR) and the genes C3, PEPD, and GPI.

1 reference

12 December 2020

Localisation on human chromosome 19 of three genes for cell surface antigens defined by monoclonal antibodies.

1 reference

12 December 2020

Linkage analysis of the apolipoprotein C2 gene and myotonic dystrophy on human chromosome 19 reveals linkage disequilibrium in a French-Canadian population

1 reference

12 December 2020

Localization of genes encoding apolipoproteins CI, CII, and E to the p13----cen region of human chromosome 19.

1 reference

12 December 2020

A multipoint linkage map around the locus for myotonic dystrophy on chromosome 19

1 reference

12 December 2020

The gene for human apolipoprotein CI is located 4.3 kilobases away from the apolipoprotein E gene on chromosome 19

1 reference

12 December 2020

Isolation and characterisation of a cDNA clone for human apolipoprotein CI and assignment of the gene to chromosome 19

1 reference

12 December 2020

Report of the committee on the genetic constitution of chromosomes 18 and 19.

1 reference

12 December 2020

Three-point linkage analysis employing C3 and 19cen markers assigns the myotonic dystrophy gene to 19q

1 reference

12 December 2020

Human apolipoprotein CI (apoC1) gene locus: DraI dimorphic site

1 reference

12 December 2020

Isolation, characterization, and mapping to chromosome 19 of the human apolipoprotein E gene.

1 reference

12 December 2020

Detection of heterozygotes for myotonic dystrophy

1 reference

12 December 2020

Human creatine kinase genes on chromosomes 15 and 19, and proximity of the gene for the muscle form to the genes for apolipoprotein C2 and excision repair

1 reference

12 December 2020

Linkage between the loci for peptidase D and cytochrome P-450 (CYP1) on chromosome 19

1 reference

12 December 2020

Further mapping of markers around the centromere of human chromosome 19

1 reference

12 December 2020

A physical map of the apolipoprotein gene cluster on human chromosome 19

1 reference

12 December 2020

Isolation and sequence of a human cytochrome P-450 cDNA clone

1 reference

12 December 2020

Apolipoprotein gene cluster on chromosome 19. Definite localization of the APOC2 gene and the polymorphic Hpa I site associated with type III hyperlipoproteinemia

1 reference

12 December 2020

Toward early diagnosis of myotonic dystrophy: construction and characterization of a somatic cell hybrid with a single human der(19) chromosome

1 reference

12 December 2020

Human apolipoprotein CI (ApoC1) gene locus: BglI dimorphic site

1 reference

12 December 2020

Identifiers

DOI

10.1007/BF00206751

1 reference

Dimensions Publication ID

13 October 2017

0 references

1 reference