Report of the DNA committee and catalogs of cloned and mapped genes and DNA polymorphisms.
about
X-linked alpha-thalassemia/mental retardation (ATR-X) syndrome: localization to Xq12-q21.31 by X inactivation and linkage analysisConfirmation of genetic heterogeneity in limb-girdle muscular dystrophy: linkage of an autosomal dominant form to chromosome 5qThe gene for Treacher Collins syndrome maps to the long arm of chromosome 5Linkage studies in familial Alzheimer disease: evidence for chromosome 19 linkageParameters of the human genomeChromosome bands, their chromatin flavors, and their functional featuresGenetic counseling in rare syndromes: a resampling method for determining an approximate confidence interval for gene location with linkage data from a single pedigree.Improved predictive test for MEN2, using flanking dinucleotide repeats and RFLPsConfirmation of clinical diagnosis in requests for prenatal prediction of SMA type I.Estimation of the size of the chromosome 17p11.2 duplication in Charcot-Marie-Tooth neuropathy type 1a (CMT1a). HMSN Collaborative Research Group.Prenatal prediction of spinal muscular atrophy.A submicroscopic translocation, t(4;10), responsible for recurrent Wolf-Hirschhorn syndrome identified by allele loss and fluorescent in situ hybridisation.Mapping of the X linked form of hyper IgM syndrome (HIGM1)Analysis of the origin of Turner's syndrome using polymorphic DNA probesMolecular studies of non-disjunction in trisomy 16.Localisation of the MRX3 gene for non-specific X linked mental retardationMap of 16 polymorphic loci on the short arm of chromosome 16 close to the polycystic kidney disease gene (PKD1)Two step procedure for early diagnosis of polycystic kidney disease with polymorphic DNA markers on both sides of the gene.Mechanisms of p53 loss in human sarcomas.Loss of heterozygosity on chromosomes 17 and 18 in breast carcinoma: two additional regions identified.Diastrophic dysplasia gene maps to the distal long arm of chromosome 5An MspI polymorphism at the DXS11 locus.Linkage analysis with markers on 17q in 29 Swedish breast cancer families.The gene responsible for X-linked cleft palate (CPX) in a British Columbia native kindred is localized between PGK1 and DXYS1.Linkage analysis of keratosis follicularis spinulosa decalvans, and regional assignment to human chromosome Xp21.2-p22.2.Dystonia-parkinsonism syndrome (XDP) locus: flanking markers in Xq12-q21.1.Waardenburg syndrome (WS): the analysis of a single family with a WS1 mutation showing linkage to RFLP markers on human chromosome 2q.Localization of the Aland Island eye disease locus to the pericentromeric region of the X chromosome by linkage analysis.X-linked nephrogenic diabetes insipidus: from the ship Hopewell to RFLP studiesHigh-resolution mapping of the X-linked hypohidrotic ectodermal dysplasia (EDA) locus.The parental origin of the single X chromosome in Turner syndrome: lack of correlation with parental age or clinical phenotype.Genetic mapping of new DNA probes at Xq27 defines a strategy for DNA studies in the fragile X syndromeOptic atrophy in Leber hereditary optic neuroretinopathy is probably determined by an X-chromosomal gene closely linked to DXS7.Linkage analysis of familial Alzheimer disease, using chromosome 21 markersAssociation of Treacher Collins syndrome and translocation 6p21.31/16p13.11: exclusion of the locus from these candidate regionsProgress in the search for genetic linkage with Tourette syndrome: an exclusion map covering more than 50% of the autosomal genome.Trisomy 21: association between reduced recombination and nondisjunction.Detecting high-resolution polymorphisms in human coding loci by combining PCR and single-strand conformation polymorphism (SSCP) analysis.XY chromosome nondisjunction in man is associated with diminished recombination in the pseudoautosomal region.Nonradioactive assay for new microsatellite polymorphisms at the 5' end of the dystrophin gene, and estimation of intragenic recombination
P2860
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P2860
Report of the DNA committee and catalogs of cloned and mapped genes and DNA polymorphisms.
description
1989 nî lūn-bûn
@nan
1989年の論文
@ja
1989年学术文章
@wuu
1989年学术文章
@zh
1989年学术文章
@zh-cn
1989年学术文章
@zh-hans
1989年学术文章
@zh-my
1989年学术文章
@zh-sg
1989年學術文章
@yue
1989年學術文章
@zh-hant
name
Report of the DNA committee an ...... d genes and DNA polymorphisms.
@ast
Report of the DNA committee an ...... d genes and DNA polymorphisms.
@en
type
label
Report of the DNA committee an ...... d genes and DNA polymorphisms.
@ast
Report of the DNA committee an ...... d genes and DNA polymorphisms.
@en
prefLabel
Report of the DNA committee an ...... d genes and DNA polymorphisms.
@ast
Report of the DNA committee an ...... d genes and DNA polymorphisms.
@en
P2093
P356
P1476
Report of the DNA committee and catalogs of cloned and mapped genes and DNA polymorphisms
@en
P2093
F Ricciuti
G Hutchings
H F Willard
J Gelernter
J Schmidtke
P304
P356
10.1159/000132810
P577
1989-01-01T00:00:00Z