scholarly article | Q13442814 |
P2093 | author name string | Richard I | |
Broux O | |||
Chiannilkulchai N | |||
Fougerousse F | |||
Pereira de Souza A | |||
Brenguier L | |||
Allamand V | |||
Bourg N | |||
Devaud C | |||
Pasturaud P | |||
P2860 | cites work | Mutations in the proteolytic enzyme calpain 3 cause limb-girdle muscular dystrophy type 2A | Q24314667 |
The diastrophic dysplasia gene encodes a novel sulfate transporter: positional cloning by fine-structure linkage disequilibrium mapping | Q24321747 | ||
Evidence of genetic heterogeneity in the autosomal recessive adult forms of limb-girdle muscular dystrophy following linkage analysis with 15q probes in Brazilian families | Q24514983 | ||
Identity-by-descent and association mapping of a recessive gene for Hirschsprung disease on human chromosome 13q22 | Q28242301 | ||
A gene for autosomal recessive limb-girdle muscular dystrophy maps to chromosome 2p | Q28243860 | ||
Localization of the EPM1 gene for progressive myoclonus epilepsy on chromosome 21: linkage disequilibrium allows high resolution mapping | Q28249374 | ||
Population frequencies of inherited neuromuscular diseases—A world survey | Q28266298 | ||
Identification of the cystic fibrosis gene: genetic analysis | Q29614402 | ||
Homozygosity mapping: a way to map human recessive traits with the DNA of inbred children | Q29615807 | ||
Multilocus linkage analysis in humans: detection of linkage and estimation of recombination | Q29620848 | ||
A second-generation linkage map of the human genome | Q33192755 | ||
A primary expression map of the chromosome 15q15 region containing the recessive form of limb-girdle muscular dystrophy (LGMD2A) gene. | Q34302048 | ||
Localization of Friedreich ataxia phenotype with selective vitamin E deficiency to chromosome 8q by homozygosity mapping | Q34345703 | ||
Molecular analysis of Hurler syndrome in Druze and Muslim Arab patients in Israel: multiple allelic mutations of the IDUA gene in a small geographic area | Q35194898 | ||
Linkage disequilibria between pairs of loci within a highly polymorphic region of chromosome 2Q. | Q35198651 | ||
Friedreich ataxia in Louisiana Acadians: demonstration of a founder effect by analysis of microsatellite-generated extended haplotypes | Q35199415 | ||
Refining the position of Wilson disease by linkage disequilibrium with polymorphic microsatellites | Q35888843 | ||
Recombinations in individuals homozygous by descent localize the Friedreich ataxia locus in a cloned 450-kb interval. | Q35889199 | ||
Linkage disequilibrium predicts physical distance in the adenomatous polyposis coli region. | Q35889324 | ||
Linkage disequilibrium in the region of the autosomal dominant polycystic kidney disease gene (PKD1). | Q35889622 | ||
Mapping of a chromosome 15 region involved in limb girdle muscular dystrophy. | Q36731351 | ||
Multiple mutations are responsible for the high frequency of metachromatic leukodystrophy in a small geographic area | Q41762644 | ||
Consanguinity in a midwestern United States isolate | Q42040466 | ||
Confirmation of linkage of limb-girdle muscular dystrophy, type 2, to chromosome 15. | Q54774379 | ||
Linkage disequilibrium mapping in isolated founder populations: diastrophic dysplasia in Finland | Q55671005 | ||
Genetic heterogeneity of autosomal recessive limbgirdle muscular dystrophy in a genetic isolate (Amish) and evidence for a new locus | Q57398301 | ||
Targeted Development of Microsatellite Markers from Inter-Alu Amplification of YAC Clones | Q57398318 | ||
A linkage map of human chromosome 15 with an average resolution of 2 cM and containing 55 polymorphic microsatellites | Q57398320 | ||
Mapping of two chromosome 15 microsatellites | Q57398354 | ||
Limb-girdle muscular dystrophy: clinical manifestations and detection of preclinical disease | Q59242124 | ||
A gene for limb-girdle muscular dystrophy maps to chromosome 15 by linkage | Q63979954 | ||
Limb-girdle syndrome: a genetic study of 22 large Brazilian families comparison with X-linked Duchenne and Becker dystrophies | Q67932796 | ||
A comprehensive human linkage map with centimorgan density. Cooperative Human Linkage Center (CHLC) | Q72202059 | ||
Homozygosity mapping of the gene for alkaptonuria to chromosome 3q2 | Q72635328 | ||
P433 | issue | 6 | |
P407 | language of work or name | English | Q1860 |
P921 | main subject | limb-girdle muscular dystrophy | Q1531322 |
P304 | page(s) | 1417-1430 | |
P577 | publication date | 1995-06-01 | |
P1433 | published in | American Journal of Human Genetics | Q4744249 |
P1476 | title | Preferential localization of the limb-girdle muscular dystrophy type 2A gene in the proximal part of a 1-cM 15q15.1-q15.3 interval | |
P478 | volume | 56 |
Q48070100 | An STS map of the limb girdle muscular dystrophy type 2A region. |
Q42036972 | Calpainopathy-a survey of mutations and polymorphisms |
Q24678754 | DNA studies of limb-girdle muscular dystrophy type 2A in the Amish exclude a modifying mitochondrial gene and show no evidence for a modifying nuclear gene |
Q34043760 | Genetic and physical mapping of the locus for autosomal dominant renal Fanconi syndrome, on chromosome 15q15.3. |
Q56459995 | Klinik und Genetik der Gliederg�rteldystrophien |
Q35882131 | Limb-girdle muscular dystrophy and Miyoshi myopathy in an aboriginal Canadian kindred map to LGMD2B and segregate with the same haplotype. |
Q34385428 | Localization of the gene for congenital dyserythropoietic anemia type I to a <1-cM interval on chromosome 15q15.1-15.3. |
Q24680877 | Multiple independent molecular etiology for limb-girdle muscular dystrophy type 2A patients from various geographical origins |
Q42588732 | Multiple mutations in a specific gene in a small geographic area: a common phenomenon? |
Q35954589 | Predicting the range of linkage disequilibrium |
Q24530091 | Recombinant expression and isolation of human L-arginine:glycine amidinotransferase and identification of its active-site cysteine residue |
Q42589339 | The Réunion paradox and the digenic model |
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