About: A comprehensive human linkage map with centimorgan density. Cooperative Human Linkage Center (CHLC)

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About: A comprehensive human linkage map with centimorgan density. Cooperative Human Linkage Center (CHLC) Goto Sponge NotDistinct Permalink

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scientific article published on 01 September 1994

Attributes	Values
rdf:type	Item
description	wetenschappelijk artikel (nl) наукова стаття, опублікована у вересні 1994 (uk) im September 1994 veröffentlichter wissenschaftlicher Artikel (de) artículu científicu espublizáu en setiembre de 1994 (ast) scientific article published on 01 September 1994 (en)
publication date	wds:Q72202059-F367B997-0FBA-4CBF-A02B-A634162CC9B9
publication date	1994-09-01 00:00:00Z (xsd:dateTime)
language of work or name	wds:Q72202059-84AC2EEF-1AC1-4DD6-8A87-1F8BF92D0611
language of work or name	English
author name string	wds:Q72202059-1017380F-0001-409A-B5E9-58AB2D8BF787 wds:Q72202059-35C53B0C-6ED7-4121-96E7-E76FA9A396D9 wds:Q72202059-3F45F7D0-9060-4951-91FC-56FC5E81E019 wds:Q72202059-88F9A04E-F5A0-46BB-B75D-7F3BE566057B wds:Q72202059-9039EB0A-583E-4E76-8A87-F1A5B0000A39 wds:Q72202059-9F5DB29C-3F57-4B72-8CA4-AE582CB9A072 wds:Q72202059-A9ABDC5F-6F97-4CA4-892F-FE2315317663 wds:Q72202059-B35A98E3-4249-40C3-A450-A1084C1DF2DC wds:Q72202059-C6916C02-C183-4E13-967E-96B1E5D34AFB wds:Q72202059-DC97EA76-BF22-44FD-B03E-DC3CFF825939
author name string	J C Murray V C Sheffield J L Weber K H Buetow G M Duyk S Sunden T Scherpbier-Heddema F Manion J Quillen S Ludwigsen
rdfs:label	A comprehensive human linkage map with centimorgan density. Cooperative Human Linkage Center (nl) A comprehensive human linkage map with centimorgan density. Cooperative Human Linkage Center (CHLC) (en)
skos:prefLabel	A comprehensive human linkage map with centimorgan density. Cooperative Human Linkage Center (nl) A comprehensive human linkage map with centimorgan density. Cooperative Human Linkage Center (CHLC) (en)
name	A comprehensive human linkage map with centimorgan density. Cooperative Human Linkage Center (nl) A comprehensive human linkage map with centimorgan density. Cooperative Human Linkage Center (CHLC) (en)
title	wds:Q72202059-9F0B1875-16CF-4567-A269-5D0D78441867
title	A comprehensive human linkage map with centimorgan density. Cooperative Human Linkage Center (CHLC) (en)
page(s)	wds:Q72202059-2563416C-5275-4043-86D5-7A827BE98A9C
page(s)	2049-2054
instance of	wds:Q72202059-93CFA71C-55B0-4C3C-A8B4-AE878C4EEEB9
instance of	scholarly article
PubMed ID	wds:Q72202059-3E8DA108-E83F-4E79-B220-31DA05C9F7AA
PubMed ID	http://rdf.ncbi.nlm.nih.gov/pubchem/reference/8091227
PubMed ID	8091227
published in	wds:Q72202059-B456290E-816C-4A48-BE06-A4337ADD7D7F
published in	Science
issue	wds:Q72202059-B537CEBB-2F6C-4BF3-8684-793B9610F2B5
volume	wds:Q72202059-E22C81E4-4D7E-4CEE-BCB0-61E26CDFBAD6
issue	5181
volume	265
DOI	wds:Q72202059-E11ACA91-622F-41C8-BEE4-A6A88512A51A
DOI	http://dx.doi.org/10.1126/SCIENCE.8091227
DOI	10.1126/SCIENCE.8091227
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q72202059
is cites work of	Identification of a chromosome 8p locus for early-onset coronary heart disease in a French Canadian population An integrated metric physical map of human chromosome 19. A genomewide screen for autism: strong evidence for linkage to chromosomes 2q, 7q, and 16p. Familial eosinophilia maps to the cytokine gene cluster on human chromosomal region 5q31-q33. Basic concepts in the study of diseases with complex genetics A highly informative SNP linkage panel for human genetic studies. Genetic approaches to stature, pubertal timing, and other complex traits Localization of common deletion regions on 1p and 19q in human gliomas and their association with histological subtype. Deletion mapping of chromosome 2 in human lung carcinoma Dominant hereditary inclusion-body myopathy gene (IBM3) maps to chromosome region 17p13.1. Autozygosity mapping, to chromosome 11q25, of a rare autosomal recessive syndrome causing histiocytosis, joint contractures, and sensorineural deafness. Pendred syndrome is caused by mutations in a putative sulphate transporter gene (PDS) Mapping of a gene for type 2 diabetes associated with an insulin secretion defect by a genome scan in Finnish families Expression-based genetic/physical maps of single-nucleotide polymorphisms identified by the cancer genome anatomy project A putative vulnerability locus to multiple sclerosis maps to 5p14-p12 in a region syntenic to the murine locus Eae2 Isolation of chromosome 18-specific brain transcripts as positional candidates for bipolar disorder An autosomal genomic scan for loci linked to type II diabetes mellitus and body-mass index in Pima Indians The forkhead transcription factor gene FKHL7 is responsible for glaucoma phenotypes which map to 6p25 A human MSX1 homeodomain missense mutation causes selective tooth agenesis Association of MSX1 and TGFB3 with nonsyndromic clefting in humans Finishing the euchromatic sequence of the human genome A high-resolution recombination map of the human genome A comprehensive genetic map of the human genome based on 5,264 microsatellites Epilepsy and mental retardation limited to females: an X-linked dominant disorder with male sparing A second middle eastern kindred with autosomal recessive non-syndromic hearing loss segregates DFNB9. Localization of the gene for familial primary pulmonary hypertension to chromosome 2q31–32 Mutations in CYP1B1, the gene for cytochrome P4501B1, are the predominant cause of primary congenital glaucoma in Saudi Arabia Mapping a gene causing cerebral cavernous malformation to 7q11.2-q21 Pendred syndrome maps to chromosome 7q21-34 and is caused by an intrinsic defect in thyroid iodine organification Linkage of congenital recessive deafness (gene DFNB10) to chromosome 21q22.3 Association mapping of disease loci, by use of a pooled DNA genomic screen Genome-wide multipoint linkage analyses of multiplex schizophrenia pedigrees from the oceanic nation of Palau Genetic mapping using haplotype, association and linkage methods suggests a locus for severe bipolar disorder (BPI) at 18q22-q23. Genomewide scan of multiple sclerosis in Finnish multiplex families SNPing away at complex diseases: analysis of single-nucleotide polymorphisms around APOE in Alzheimer disease A frameshift polymorphism in P2X5 elicits an allogeneic cytotoxic T lymphocyte response associated with remission of chronic myeloid leukemia Identification of a polymorphic gene, BCL2A1, encoding two novel hematopoietic lineage-specific minor histocompatibility antigens Association of specific language impairment (SLI) to the region of 7q31. Autosomal dominant iridogoniodysgenesis anomaly maps to 6p25 Retinal degeneration characterizes a spinocerebellar ataxia mapping to chromosome 3p. Homologous recombination of a flanking repeat gene cluster is a mechanism for a common contiguous gene deletion syndrome Fine mapping of the congenital chloride diarrhea gene by linkage disequilibrium Smallest region of overlapping deletion in 1p36 in human neuroblastoma: a 1 Mbp cosmid and PAC contig Detailed molecular analysis of 1p36 in neuroblastoma Homozygosity mapping identifies an additional locus for Wolfram syndrome on chromosome 4q

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