| pubmed-article:10066388 | rdf:type | pubmed:Citation | lld:pubmed |
| pubmed-article:10066388 | lifeskim:mentions | umls-concept:C0205147 | lld:lifeskim |
| pubmed-article:10066388 | lifeskim:mentions | umls-concept:C1708726 | lld:lifeskim |
| pubmed-article:10066388 | lifeskim:mentions | umls-concept:C1520996 | lld:lifeskim |
| pubmed-article:10066388 | lifeskim:mentions | umls-concept:C0342287 | lld:lifeskim |
| pubmed-article:10066388 | lifeskim:mentions | umls-concept:C0475264 | lld:lifeskim |
| pubmed-article:10066388 | pubmed:issue | 3 | lld:pubmed |
| pubmed-article:10066388 | pubmed:dateCreated | 1999-4-13 | lld:pubmed |
| pubmed-article:10066388 | pubmed:abstractText | Thiamine-responsive megaloblastic anemia (TRMA) is a rare autosomal recessive syndrome characterized by megaloblastic anemia, deafness, and diabetes mellitus. A genome scan previously established linkage of this disorder to 1q23 and haplotype analysis defined a 16-cM critical region. Molecular genetic analyses of four unrelated multiplex Iranian families inheriting TRMA confirmed linkage to the same region and identified recombinant chromosomes which permitted refinement of the critical region to a narrow 1.4-cM interval. The haplotypes of the families differed, consistent with at least two independent mutational events. This refinement of the TRMA locus to less than 10% of that previously published should markedly facilitate the identification and evaluation of positional candidate and novel genes which may cause this disorder. | lld:pubmed |
| pubmed-article:10066388 | pubmed:grant | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:10066388 | pubmed:grant | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:10066388 | pubmed:language | eng | lld:pubmed |
| pubmed-article:10066388 | pubmed:journal | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:10066388 | pubmed:citationSubset | IM | lld:pubmed |
| pubmed-article:10066388 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:10066388 | pubmed:status | MEDLINE | lld:pubmed |
| pubmed-article:10066388 | pubmed:month | Mar | lld:pubmed |
| pubmed-article:10066388 | pubmed:issn | 1096-7192 | lld:pubmed |
| pubmed-article:10066388 | pubmed:author | pubmed-author:DesnickR JRJ | lld:pubmed |
| pubmed-article:10066388 | pubmed:author | pubmed-author:VossoughPP | lld:pubmed |
| pubmed-article:10066388 | pubmed:author | pubmed-author:JalaliMM | lld:pubmed |
| pubmed-article:10066388 | pubmed:author | pubmed-author:GelbB DBD | lld:pubmed |
| pubmed-article:10066388 | pubmed:author | pubmed-author:DiazG AGA | lld:pubmed |
| pubmed-article:10066388 | pubmed:author | pubmed-author:BanikazemiMM | lld:pubmed |
| pubmed-article:10066388 | pubmed:copyrightInfo | Copyright 1999 Academic Press. | lld:pubmed |
| pubmed-article:10066388 | pubmed:issnType | Print | lld:pubmed |
| pubmed-article:10066388 | pubmed:volume | 66 | lld:pubmed |
| pubmed-article:10066388 | pubmed:owner | NLM | lld:pubmed |
| pubmed-article:10066388 | pubmed:authorsComplete | Y | lld:pubmed |
| pubmed-article:10066388 | pubmed:pagination | 193-8 | lld:pubmed |
| pubmed-article:10066388 | pubmed:dateRevised | 2010-11-18 | lld:pubmed |
| pubmed-article:10066388 | pubmed:meshHeading | pubmed-meshheading:10066388... | lld:pubmed |
| pubmed-article:10066388 | pubmed:meshHeading | pubmed-meshheading:10066388... | lld:pubmed |
| pubmed-article:10066388 | pubmed:meshHeading | pubmed-meshheading:10066388... | lld:pubmed |
| pubmed-article:10066388 | pubmed:meshHeading | pubmed-meshheading:10066388... | lld:pubmed |
| pubmed-article:10066388 | pubmed:meshHeading | pubmed-meshheading:10066388... | lld:pubmed |
| pubmed-article:10066388 | pubmed:meshHeading | pubmed-meshheading:10066388... | lld:pubmed |
| pubmed-article:10066388 | pubmed:meshHeading | pubmed-meshheading:10066388... | lld:pubmed |
| pubmed-article:10066388 | pubmed:meshHeading | pubmed-meshheading:10066388... | lld:pubmed |
| pubmed-article:10066388 | pubmed:meshHeading | pubmed-meshheading:10066388... | lld:pubmed |
| pubmed-article:10066388 | pubmed:meshHeading | pubmed-meshheading:10066388... | lld:pubmed |
| pubmed-article:10066388 | pubmed:meshHeading | pubmed-meshheading:10066388... | lld:pubmed |
| pubmed-article:10066388 | pubmed:year | 1999 | lld:pubmed |
| pubmed-article:10066388 | pubmed:articleTitle | Localization of the thiamine-responsive megaloblastic anemia syndrome locus to a 1.4-cM region of 1q23. | lld:pubmed |
| pubmed-article:10066388 | pubmed:affiliation | Department of Human Genetics, Mount Sinai School of Medicine, New York, New York 10029, USA. | lld:pubmed |
| pubmed-article:10066388 | pubmed:publicationType | Journal Article | lld:pubmed |
| pubmed-article:10066388 | pubmed:publicationType | Research Support, U.S. Gov't, P.H.S. | lld:pubmed |
| http://linkedlifedata.com/r... | pubmed:referesTo | pubmed-article:10066388 | lld:pubmed |
