about
Mutations in the gene encoding the human matrix Gla protein cause Keutel syndromeEvidence for heterogeneity in recombination in the human pseudoautosomal region: high resolution analysis by sperm typing and radiation-hybrid mapping.Homozygosity mapping of a gene locus for primary ciliary dyskinesia on chromosome 5p and identification of the heavy dynein chain DNAH5 as a candidate geneLong homozygous chromosomal segments in reference families from the centre d'Etude du polymorphisme humainShwachman-Diamond syndrome with exocrine pancreatic dysfunction and bone marrow failure maps to the centromeric region of chromosome 7.The gene for glycogen-storage disease type 1b maps to chromosome 11q23.A gene for autosomal recessive limb-girdle muscular dystrophy in Manitoba Hutterites maps to chromosome region 9q31-q33: evidence for another limb-girdle muscular dystrophy locus.Mutation in the human acetylcholinesterase-associated collagen gene, COLQ, is responsible for congenital myasthenic syndrome with end-plate acetylcholinesterase deficiency (Type Ic)Assignment of the muscle-eye-brain disease gene to 1p32-p34 by linkage analysis and homozygosity mapping.Identification of a new gene locus for adolescent nephronophthisis, on chromosome 3q22 in a large Venezuelan pedigree.Hereditary hypophosphatemic rickets with hypercalciuria is caused by mutations in the sodium-phosphate cotransporter gene SLC34A3.A draft annotation and overview of the human genomeLimiting the location of putative human prostate cancer tumor suppressor genes on chromosome 18qA major locus for fasting insulin concentrations and insulin resistance on chromosome 6q with strong pleiotropic effects on obesity-related phenotypes in nondiabetic Mexican AmericansImpact of population structure, effective bottleneck time, and allele frequency on linkage disequilibrium mapsPooled analysis of loss of heterozygosity in breast cancer: a genome scan provides comparative evidence for multiple tumor suppressors and identifies novel candidate regions.A comprehensive, high-resolution genomic transcript map of human skeletal muscle.A genome-wide search for chromosomal loci linked to mental health wellness in relatives at high risk for bipolar affective disorder among the Old Order Amish.Linkage disequilibrium maps and association mapping.HLA haplotypes and microsatellite polymorphisms in and around the major histocompatibility complex region in a Native American population with a high prevalence of scleroderma (systemic sclerosis).A map of the human genome in linkage disequilibrium units.Quantification of homozygosity in consanguineous individuals with autosomal recessive disease.The first linkage disequilibrium (LD) maps: delineation of hot and cold blocks by diplotype analysis.A schizophrenia-susceptibility locus at 6q25, in one of the world's largest reported pedigrees.Localization of a susceptibility gene for familial nonmedullary thyroid carcinoma to chromosome 2q21Fine mapping of the locus for Shwachman-Diamond syndrome at 7q11, identification of shared disease haplotypes, and exclusion of TPST1 as a candidate gene.Detection of chromosomal aberrations by a whole-genome microsatellite screenJoint multipoint linkage analysis of multivariate qualitative and quantitative traits. II. Alcoholism and event-related potentialsPitfalls in homozygosity mapping.A 122.5-kilobase deletion of the P gene underlies the high prevalence of oculocutaneous albinism type 2 in the Navajo population.Assignment of the tibial muscular dystrophy locus to chromosome 2q31.Linkage and association between inflammatory bowel disease and a locus on chromosome 12Genome scan for human obesity and linkage to markers in 20q13.Brachydactyly type B: linkage to chromosome 9q22 and evidence for genetic heterogeneityCongenital motor nystagmus linked to Xq26-q27.Location score and haplotype analyses of the locus for autosomal recessive spastic ataxia of Charlevoix-Saguenay, in chromosome region 13q11.Retinitis pigmentosa and progressive sensorineural hearing loss caused by a C12258A mutation in the mitochondrial MTTS2 gene.Linkage of type 2 diabetes mellitus and of age at onset to a genetic location on chromosome 10q in Mexican Americans.A locus for isolated cleft palate, located on human chromosome 2q32Characterization of human crossover interference.
P2860
Q22008705-DA8F9399-7B6C-4260-926F-B7B04E309AF8Q22066142-A1171C75-9B92-44D0-9DB5-34C694957E41Q24290475-ED9CBFF2-458B-441B-AEF1-24A8C9233660Q24534369-0FA1B5E0-4118-44F3-B886-D234910F8C4CQ24536337-D53CF09B-DAA0-4781-9D48-3420929A31E4Q24538761-16CB532B-3EB7-4802-9406-90BCFE8B51EBQ24539083-56769EBE-A742-452D-9828-65F61E00234CQ24539214-CBF86C7B-0CAE-4C2C-BAEA-147641A77D59Q24540040-3A826E2B-BB8C-4357-9EEE-F070842A1BEDQ24540483-36D11510-1F33-4BA6-AB11-4C871E5EDD6AQ24540520-9844C2D2-1455-4EF8-8850-06919E1DDC87Q24803626-F0C47C1B-DED6-42B6-9627-4A1CE5A68B5CQ28201487-CB5AB8EA-B1B8-49DF-B026-17DF7F0278FFQ28361785-0E8F17E5-5008-4459-BF86-ECCB25228437Q28770047-B698D582-D14E-4580-BD2F-25EC3154402CQ30476046-01044E55-4E20-48B9-8FE7-06EB3CEBF301Q32028965-5D012932-74A4-4301-A1F7-C1E2A5811579Q33595430-C5943D8F-51CD-4FE6-8BCD-FFCC643E55ACQ33831968-53F0B7EE-7CA2-4ADC-9C07-6B8750226EF1Q33855367-5247BC4E-8A96-40C2-AC45-EED729B988ABQ33920233-ED0BAB0E-BD02-48A3-B62B-9BC1D9D950D2Q33995399-5613B77D-3AFA-471F-8326-2A3BB3F686CBQ34012852-B9EFA785-227D-4758-AABE-B26A77E44A42Q34020480-543E5E6D-23C3-4E03-A9ED-AE14491B36BBQ34044355-0E7CAC4B-ECD0-4CF6-9EFA-8BF3C0991063Q34130421-9A92AA7C-FC54-4B2A-9C63-424222AAEC27Q34145029-A895547F-3D58-4672-8E81-DA65FA85899CQ34145771-A96726F4-CB9E-48D9-8E5E-ED54A51FE4A9Q34146855-CC15D6E7-CE77-492D-8ABB-BC2ABF18B6FDQ34354851-70C0094B-8D7E-4CB1-BC60-07D629CA564BQ34384680-3F31EC21-5CCB-4C24-BE00-753069C40D64Q34386242-4352A908-A0C1-40D6-9F01-80A3E2CD93B3Q34388612-20962B13-C0D9-419A-A15D-814B569757CEQ34388946-E201F068-6920-4967-A979-8BDCD3F11282Q34388974-0F484B28-8FAB-4243-BF1D-20D2F69394AFQ34389112-EB265E24-19E1-40B9-B9AA-BCD77C3D1D84Q34389296-06ED0CD2-60A6-4A88-9B2E-F49EDB34CE49Q34389390-BCF7B9A9-83BE-4A49-8951-962F9C8470D2Q34389952-C534F41D-305D-46B1-AD72-CECC546DF354Q34390700-D3CE37E5-C5AB-4AE9-8184-14AD063C0132
P2860
description
article científic
@ca
article scientifique
@fr
articolo scientifico
@it
artigo científico
@pt
bilimsel makale
@tr
scientific article published on December 1996
@en
vedecký článok
@sk
vetenskaplig artikel
@sv
videnskabelig artikel
@da
vědecký článek
@cs
name
A metric map of humans: 23,500 loci in 850 bands.
@en
A metric map of humans: 23,500 loci in 850 bands.
@nl
type
label
A metric map of humans: 23,500 loci in 850 bands.
@en
A metric map of humans: 23,500 loci in 850 bands.
@nl
prefLabel
A metric map of humans: 23,500 loci in 850 bands.
@en
A metric map of humans: 23,500 loci in 850 bands.
@nl
P2093
P2860
P356
P1476
A metric map of humans: 23,500 loci in 850 bands.
@en
P2093
P2860
P304
14771-14775
P356
10.1073/PNAS.93.25.14771
P407
P577
1996-12-01T00:00:00Z