Evidence for human meiotic recombination interference obtained through construction of a short tandem repeat-polymorphism linkage map of chromosome 19.
about
Genetic mapping of a locus for multiple epiphyseal dysplasia (EDM2) to a region of chromosome 1 containing a type IX collagen geneGenetic linkage mapping of multiple epiphyseal dysplasia to the pericentromeric region of chromosome 19Genetic heterogeneity in multiple epiphyseal dysplasiaCongenital non-syndromal autosomal recessive deafness in Bengkala, an isolated Balinese villageCharacterization of human crossover interference.Genomewide search for genes influencing percent body fat in Pima Indians: suggestive linkage at chromosome 11q21-q22. Pima Diabetes Gene GroupA strategy for constructing high-resolution genetic maps of the human genome: a genetic map of chromosome 17p, ordered with meiotic breakpoint-mapping panelsFine mapping and haplotype analysis of the locus for congenital nephrotic syndrome on chromosome 19q13.1.Genomic structural variants are linked with intellectual disability.HHV-8-unrelated primary effusion-like lymphoma associated with clonal loss of inherited chromosomally-integrated human herpesvirus-6A from the telomere of chromosome 19q.Evidence for dysregulation of genome-wide recombination in oocytes with nondisjoined chromosomes 21.Refinement of the cone-rod retinal dystrophy locus on chromosome 19q.Refinement of the OPA1 gene locus on chromosome 3q28-q29 to a region of 2-8 cM, in one Cuban pedigree with autosomal dominant optic atrophy type Kjer.Improved set of short-tandem-repeat polymorphisms for screening the human genome.Genetic maps of microsatellite and single-nucleotide polymorphism markers: are the distances accurate?
P2860
Q24672816-B61B2F09-A9DE-443F-AFA1-5B2A2F02DD7EQ24673288-BC3CB1A0-DF13-48E3-8915-14F8A32C3F18Q30445330-F99AC71E-D681-4AFA-A64E-F60C555CBC82Q33676549-F6E3B25D-76F0-4504-9CE7-13914DFF3950Q34390700-84007A63-5D92-49A4-A406-D46EE079035CQ35239263-BC0BCAC9-8172-49B3-90BA-DB129BCD49B7Q35643093-09F2B7F3-7951-4ACC-B9AC-434332517638Q35644101-F19EF854-0557-4DE0-8DD6-3213E451C770Q35897520-C1E37A5E-486D-4AEF-93EA-7F400A5F6D08Q36656811-0C2A14B4-55A1-49B8-8B19-A32F74638635Q37406436-6FC8B2D5-C029-42C3-AC1F-3486DC117CC3Q42558158-480F1156-1CF4-49FB-AD4E-882B525C2E51Q42950881-7B33305E-F6D7-42A2-BC93-03DFDFCBB6EAQ43109070-B6A63B52-229D-4BEB-9814-570F47BF9D17Q52950187-CF6CF40B-B214-4544-BC17-857045C34CDA
P2860
Evidence for human meiotic recombination interference obtained through construction of a short tandem repeat-polymorphism linkage map of chromosome 19.
description
1993 nî lūn-bûn
@nan
1993 թուականի Նոյեմբերին հրատարակուած գիտական յօդուած
@hyw
1993 թվականի նոյեմբերին հրատարակված գիտական հոդված
@hy
1993年の論文
@ja
1993年論文
@yue
1993年論文
@zh-hant
1993年論文
@zh-hk
1993年論文
@zh-mo
1993年論文
@zh-tw
1993年论文
@wuu
name
Evidence for human meiotic rec ...... linkage map of chromosome 19.
@ast
Evidence for human meiotic rec ...... linkage map of chromosome 19.
@en
type
label
Evidence for human meiotic rec ...... linkage map of chromosome 19.
@ast
Evidence for human meiotic rec ...... linkage map of chromosome 19.
@en
prefLabel
Evidence for human meiotic rec ...... linkage map of chromosome 19.
@ast
Evidence for human meiotic rec ...... linkage map of chromosome 19.
@en
P2093
P2860
P1476
Evidence for human meiotic rec ...... linkage map of chromosome 19.
@en
P2093
B F Brandriff
M Stephenson
N C Dracopoli
P J Wilkie
P2860
P304
P407
P577
1993-11-01T00:00:00Z