European Gene Mapping Project (EUROGEM): Breakpoint panels for human chromosomes based on the CEPH reference families (Q58673420)

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English	European Gene Mapping Project (EUROGEM): Breakpoint panels for human chromosomes based on the CEPH reference families	article

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31 October 2019

European Gene Mapping Project (EUROGEM): breakpoint panels for human chromosomes based on the CEPH reference families. Centre d'Etude du Polymorphisme Humain (English)

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31 October 2019

Nicholas K Moschonas

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31 October 2019

Gilles Vergnaud

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31 October 2019

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S A Cox

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31 October 2019

J Attwood

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31 October 2019

S P Bryant

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31 October 2019

R Bains

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31 October 2019

S Povey

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31 October 2019

M Rebello

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31 October 2019

M Kapsetaki

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31 October 2019

K H Grzeschik

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31 October 2019

M Otto

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31 October 2019

M Dixon

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31 October 2019

H E Sudworth

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31 October 2019

R F Kooy

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31 October 2019

A Wright

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31 October 2019

P Teague

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31 October 2019

L Terrenato

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31 October 2019

S Monfouilloux

18

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31 October 2019

J Weissenbach

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31 October 2019

O Alibert

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31 October 2019

C Dib

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31 October 2019

S Fauré

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31 October 2019

E Bakker

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31 October 2019

N M Pearson

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31 October 2019

N K Spurr

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31 October 2019

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publication date

1 November 1996

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31 October 2019

Annals of Human Genetics

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31 October 2019

60

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31 October 2019

6

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31 October 2019

447-486

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31 October 2019

A cyclophilin-related protein involved in the function of natural killer cells

1 reference

https://api.crossref.org/works/10.1111%2FJ.1469-1809.1996.TB01614.X

21 January 2018

CEPH Consortium Map of Chromosome 9

1 reference

https://api.crossref.org/works/10.1111%2FJ.1469-1809.1996.TB01614.X

21 January 2018

An exonic mutation in the HuP2 paired domain gene causes Waardenburg's syndrome

1 reference

https://api.crossref.org/works/10.1111%2FJ.1469-1809.1996.TB01614.X

21 January 2018

A linkage map of human chromosome 15 with an average resolution of 2 cM and containing 55 polymorphic microsatellites

1 reference

https://api.crossref.org/works/10.1111%2FJ.1469-1809.1996.TB01614.X

21 January 2018

The CEPH consortium linkage map of human chromosome 15q

1 reference

https://api.crossref.org/works/10.1111%2FJ.1469-1809.1996.TB01614.X

21 January 2018

The CEPH Consortium Linkage Map of Human Chromosome 13

1 reference

https://api.crossref.org/works/10.1111%2FJ.1469-1809.1996.TB01614.X

21 January 2018

Integrated human genome-wide maps constructed using the CEPH reference panel.

1 reference

https://api.crossref.org/works/10.1111%2FJ.1469-1809.1996.TB01614.X

21 January 2018

Mapping of a locus for progressive familial intrahepatic cholestasis (Byler disease) to 18q21-q22, the benign recurrent intrahepatic cholestasis region

1 reference

https://api.crossref.org/works/10.1111%2FJ.1469-1809.1996.TB01614.X

21 January 2018

Centre d'etude du polymorphisme humain (CEPH): collaborative genetic mapping of the human genome

1 reference

https://api.crossref.org/works/10.1111%2FJ.1469-1809.1996.TB01614.X

21 January 2018

Cloning of the human heparan sulfate-N-deacetylase/N-sulfotransferase gene from the Treacher Collins syndrome candidate region at 5q32-q33.1

1 reference

https://api.crossref.org/works/10.1111%2FJ.1469-1809.1996.TB01614.X

21 January 2018

A genetic linkage map of the human genome.

1 reference

https://api.crossref.org/works/10.1111%2FJ.1469-1809.1996.TB01614.X

21 January 2018

The CEPH consortium linkage map of human chromosome 1

1 reference

https://api.crossref.org/works/10.1111%2FJ.1469-1809.1996.TB01614.X

21 January 2018

The Bloom's syndrome gene product is homologous to RecQ helicases

1 reference

https://api.crossref.org/works/10.1111%2FJ.1469-1809.1996.TB01614.X

21 January 2018

Homozygotes for CDKN2 (p16) germline mutation in Dutch familial melanoma kindreds

1 reference

https://api.crossref.org/works/10.1111%2FJ.1469-1809.1996.TB01614.X

21 January 2018

The 1993-94 Généthon human genetic linkage map

1 reference

https://api.crossref.org/works/10.1111%2FJ.1469-1809.1996.TB01614.X

21 January 2018

The diastrophic dysplasia gene encodes a novel sulfate transporter: positional cloning by fine-structure linkage disequilibrium mapping

1 reference

https://api.crossref.org/works/10.1111%2FJ.1469-1809.1996.TB01614.X

21 January 2018

Definition of a tumor suppressor locus within human chromosome 3p21-p22

1 reference

https://api.crossref.org/works/10.1111%2FJ.1469-1809.1996.TB01614.X

21 January 2018

The CEPH consortium linkage map of human chromosome 16

1 reference

https://api.crossref.org/works/10.1111%2FJ.1469-1809.1996.TB01614.X

21 January 2018

Apoptosis regulatory gene NEDD2 maps to human chromosome segment 7q34-35, a region frequently affected in haematological neoplasms

1 reference

https://api.crossref.org/works/10.1111%2FJ.1469-1809.1996.TB01614.X

21 January 2018

The CEPH Consortium Linkage Map of Human Chromosome 11

1 reference

https://api.crossref.org/works/10.1111%2FJ.1469-1809.1996.TB01614.X

21 January 2018

Automated construction of genetic linkage maps using an expert system (MultiMap): a human genome linkage map.

1 reference

https://api.crossref.org/works/10.1111%2FJ.1469-1809.1996.TB01614.X

21 January 2018

An extended genetic linkage map and an "index" map for human chromosome 17.

1 reference

https://api.crossref.org/works/10.1111%2FJ.1469-1809.1996.TB01614.X

21 January 2018

Construction of a 2.8-megabase yeast artificial chromosome contig and cloning of the human methylthioadenosine phosphorylase gene from the tumor suppressor region on 9p21

1 reference

https://api.crossref.org/works/10.1111%2FJ.1469-1809.1996.TB01614.X

21 January 2018

Nonrandom chromosomal abnormalities in primary uveal melanoma

1 reference

https://api.crossref.org/works/10.1111%2FJ.1469-1809.1996.TB01614.X

21 January 2018

Error filtration, interference, and the human linkage map

1 reference

https://api.crossref.org/works/10.1111%2FJ.1469-1809.1996.TB01614.X

21 January 2018

The CEPH consortium linkage map of human chromosome 2

1 reference

https://api.crossref.org/works/10.1111%2FJ.1469-1809.1996.TB01614.X

21 January 2018

Waardenburg's syndrome patients have mutations in the human homologue of the Pax-3 paired box gene

1 reference

https://api.crossref.org/works/10.1111%2FJ.1469-1809.1996.TB01614.X

21 January 2018

Localization to chromosome 7q36.1 of the human XRCC2 gene, determining sensitivity to DNA-damaging agents

1 reference

https://api.crossref.org/works/10.1111%2FJ.1469-1809.1996.TB01614.X

21 January 2018

Alpha-tropomyosin and cardiac troponin T mutations cause familial hypertrophic cardiomyopathy: a disease of the sarcomere

1 reference

https://api.crossref.org/works/10.1111%2FJ.1469-1809.1996.TB01614.X

21 January 2018

Report of the Second International Workshop on Human Chromosome 6.

1 reference

https://api.crossref.org/works/10.1111%2FJ.1469-1809.1996.TB01614.X

21 January 2018

A second-generation linkage map of the human genome

1 reference

https://api.crossref.org/works/10.1111%2FJ.1469-1809.1996.TB01614.X

21 January 2018

The CEPH consortium primary linkage map of human chromosome 10

1 reference

https://api.crossref.org/works/10.1111%2FJ.1469-1809.1996.TB01614.X

21 January 2018

Deletion mapping reveals two regions of chromosome 8 allele loss in colorectal carcinomas.

1 reference

https://api.crossref.org/works/10.1111%2FJ.1469-1809.1996.TB01614.X

21 January 2018

Localization of a novel natural killer triggering receptor locus to human chromosome 3p23-p21 and mouse chromosome 9.

1 reference

https://api.crossref.org/works/10.1111%2FJ.1469-1809.1996.TB01614.X

21 January 2018

(C-A)n microsatellite repeat D7S522 is the most commonly deleted region in human primary breast cancer

1 reference

https://api.crossref.org/works/10.1111%2FJ.1469-1809.1996.TB01614.X

21 January 2018

Positional cloning of the mouse obese gene and its human homologue

1 reference

https://api.crossref.org/works/10.1111%2FJ.1469-1809.1996.TB01614.X

21 January 2018

Identifiers

10.1111/J.1469-1809.1996.TB01614.X

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9024576%20AND%20SRC:MED&resulttype=core&format=json

31 October 2019

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9024576%20AND%20SRC:MED&resulttype=core&format=json

31 October 2019

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