about
Ancient and recent positive selection transformed opioid cis-regulation in humansHuman genetics and genomics a decade after the release of the draft sequence of the human genomeCoexpression of the KCNA3B gene product with Kv1.5 leads to a novel A-type potassium channelThe genetics of inflammatory bowel diseaseFibroblast growth factor-10 is a mitogen for urothelial cellsAutosomal dominant hypocalcaemia caused by a Ca(2+)-sensing receptor gene mutationIdentification and characterization of the human homologue of the short PDE4A cAMP-specific phosphodiesterase RD1 (PDE4A1) by analysis of the human HSPDE4A gene locus located at chromosome 19p13.2Disease gene mapping in isolated human populations: the example of FinlandA new X linked recessive deafness syndrome with blindness, dystonia, fractures, and mental deficiency is linked to Xq22.A mutation in COL9A1 causes multiple epiphyseal dysplasia: further evidence for locus heterogeneityMapping of primary congenital lymphedema to the 5q35.3 regionA new locus for autosomal dominant "pure" hereditary spastic paraplegia mapping to chromosome 12q13, and evidence for further genetic heterogeneityCOL9A3: A third locus for multiple epiphyseal dysplasia.The genetic basis of Weber-Cockayne epidermolysis bullosa simplex(C-A)n microsatellite repeat D7S522 is the most commonly deleted region in human primary breast cancerThe human Major Histocompatibility Complex as a paradigm in genomics researchA 3-Mb contig from D11S987 to MLK3, a gene-rich region in 11q13Meis1, a PBX1-related homeobox gene involved in myeloid leukemia in BXH-2 miceEquilibrium distributions of microsatellite repeat length resulting from a balance between slippage events and point mutationsGenetic heterogeneity in benign familial neonatal convulsions: identification of a new locus on chromosome 8qSeven new mutations in hMSH2, an HNPCC gene, identified by denaturing gradient-gel electrophoresisMutations in the human Ca(2+)-sensing-receptor gene that cause familial hypocalciuric hypercalcemiaLocalization of a gene for autosomal dominant Larsen syndrome to chromosome region 3p21.1-14.1 in the proximity of, but distinct from, the COL7A1 locusMapping of a gene for long QT syndrome to chromosome 4q25-27Autosomal dominant familial spastic paraplegia: tight linkage to chromosome 15qThe gene for spinal cerebellar ataxia 3 (SCA3) is located in a region of approximately 3 cM on chromosome 14q24.3-q32.2A gene for distal arthrogryposis type I maps to the pericentromeric region of chromosome 9Hereditary hyperparathyroidism-jaw tumor syndrome: the endocrine tumor gene HRPT2 maps to chromosome 1q21-q31Genetic mapping of a locus for multiple epiphyseal dysplasia (EDM2) to a region of chromosome 1 containing a type IX collagen geneEvidence for locus heterogeneity in human autosomal dominant split hand/split foot malformationThe genetic locus for free sialic acid storage disease maps to the long arm of chromosome 6Hypokalemic periodic paralysis and the dihydropyridine receptor (CACNL1A3): genotype/phenotype correlations for two predominant mutations and evidence for the absence of a founder effect in 16 caucasian familiesGenetic linkage mapping of multiple epiphyseal dysplasia to the pericentromeric region of chromosome 19A spectrum of mutations in the second gene for autosomal dominant polycystic kidney disease (PKD2)A haplotype map of the human genomeAssignment of the mulibrey nanism gene to 17q by linkage and linkage-disequilibrium analysisHaim-Munk syndrome and Papillon-Lefèvre syndrome are allelic mutations in cathepsin CLocalisation of a gene for prepubertal periodontitis to chromosome 11q14 and identification of a cathepsin C gene mutationTPMD: a database and resources of microsatellite marker genotyped in Taiwanese populationsTwo modes of microsatellite instability in human cancer: differential connection of defective DNA mismatch repair to dinucleotide repeat instability.
P2860
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P2860
description
1992 nî lūn-bûn
@nan
1992 թուականի Հոկտեմբերին հրատարակուած գիտական յօդուած
@hyw
1992 թվականի հոտեմբերին հրատարակված գիտական հոդված
@hy
1992年の論文
@ja
1992年論文
@yue
1992年論文
@zh-hant
1992年論文
@zh-hk
1992年論文
@zh-mo
1992年論文
@zh-tw
1992年论文
@wuu
name
A second-generation linkage map of the human genome.
@ast
A second-generation linkage map of the human genome.
@en
type
label
A second-generation linkage map of the human genome.
@ast
A second-generation linkage map of the human genome.
@en
prefLabel
A second-generation linkage map of the human genome.
@ast
A second-generation linkage map of the human genome.
@en
P2093
P356
P1433
P1476
A second-generation linkage map of the human genome.
@en
P2093
Millasseau P
Morissette J
Vaysseix G
Weissenbach J
P2888
P304
P356
10.1038/359794A0
P407
P50
P577
1992-10-01T00:00:00Z
P6179
1024780178