Structure and linkage of the D2 dopamine receptor and neural cell adhesion molecule genes on human chromosome 11q23. (Q31042635)

28 June 2017

title

Structure and linkage of the D2 dopamine receptor and neural cell adhesion molecule genes on human chromosome 11q23. (English)

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28 June 2017

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Eubanks JH

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28 June 2017

Djabali M

2

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28 June 2017

Selleri L

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28 June 2017

Grandy DK

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28 June 2017

Civelli O

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McElligott DL

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28 June 2017

Evans GA

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28 June 2017

language of work or name

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1 December 1992

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28 June 2017

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volume

14

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issue

4

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28 June 2017

page(s)

1010-1018

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Localization of the gene encoding R kappa B (NFRKB), a tissue-specific DNA binding protein, to chromosome 11q24-q25

28 June 2017

cites work

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Cloning of large segments of exogenous DNA into yeast by means of artificial chromosome vectors

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cDNA sequence and genomic structure of EV12B, a gene lying within an intron of the neurofibromatosis type 1 gene

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Separation of large DNA molecules by contour-clamped homogeneous electric fields

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Genetic linkage is excluded for the D2-dopamine receptor lambda HD2G1 and flanking loci on chromosome 11q22-q23 in Tourette syndrome.

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7 January 2021

Interferon and c-ets-1 genes in the translocation (9;11)(p22;q23) in human acute monocytic leukemia

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A simple method for the direct use of total cosmid clones as hybridization probes

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7 January 2021

Isolation, localization, and physical mapping of a highly polymorphic locus on human chromosome 11q13

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Localization of the D5 dopamine receptor gene to human chromosome 4p15.1-p15.3, centromeric to the Huntington's disease locus

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Molecular organization of the human CD3 gene family on chromosome 11q23.

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High efficiency vectors for cosmid microcloning and genomic analysis

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Analysis of the Structure and Expression of the Human Dopamine D2AReceptor Gene

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Localization of an ataxia-telangiectasia gene to chromosome 11q22-23.

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Gilles de la Tourette Syndrome Is Not Linked to D2-Dopamine Receptor

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Detection and characterization of additional DNA polymorphisms in the dopamine D2 receptor gene

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7 January 2021

Genetic heterogeneity in tuberous sclerosis

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Multiple endocrine neoplasia type 1 gene maps to chromosome 11 and is lost in insulinoma

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High-resolution mapping of human chromosome 11 by in situ hybridization with cosmid clones

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Fine mapping of the chromosome 11q22-23 region using PFGE, linkage and haplotype analysis; localization of the gene for ataxia telangiectasia to a 5cM region flanked by NCAM/DRD2 and STMY/CJ52.75, phi 2.22

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7 January 2021

No linkage between D2 dopamine receptor gene region and schizophrenia

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Chromosomal in situ hybridization using yeast artificial chromosomes

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Mapping of a gene determining tuberous sclerosis to human chromosome 11q14-11q23.

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7 January 2021

Association within a family of a balanced autosomal translocation with major mental illness

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7 January 2021

The chromosomal analysis of human solid tumors. A triple challenge

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7 January 2021

The gene encoding the oligodendrocyte-myelin glycoprotein is embedded within the neurofibromatosis type 1 gene

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7 January 2021

The ATC (ataxia-telangiectasia complementation group C) locus localizes to 11q22–q23

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7 January 2021

10.1016/S0888-7543(05)80124-7

Identifiers

DOI

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28 June 2017

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