Chromosome in situ suppression hybridisation in human male meiosis. - Wikidata - wikimedia - TriplyDB

Chromosome in situ suppression hybridisation in human male meiosis.

Chromosome in situ suppression hybridisation in human male meiosis.

http://www.wikidata.org/entity/Q33222695

about

Chromosome painting reveals asynaptic full alignment of homologs and HIM-8-dependent remodeling of X chromosome territories during Caenorhabditis elegans meiosis Meiotic studies of a human male carrier of the common translocation, t(11;22), suggests postzygotic selection rather than preferential 3:1 MI segregation as the cause of liveborn offspring with an unbalanced translocation.On the origin of crossover interference: A chromosome oscillatory movement (COM) model Meiotic segregation, recombination, and gamete aneuploidy assessed in a t(1;10)(p22.1;q22.3) reciprocal translocation carrier by three- and four-probe multicolor FISH in sperm.Altered bivalent positioning in metaphase I human spermatocytes from Robertsonian translocation carriers.Demystified ... FISH.Studies of male and female meiosis in inv(4)(p1.4;q2.3) pig carriers.

P2860

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P2860

Chromosome in situ suppression hybridisation in human male meiosis.

http://www.wikidata.org/entity/Q33222695

description

1992 nî lūn-bûn

@nan

1992 թուականի Փետրուարին հրատարակուած գիտական յօդուած

@hyw

1992 թվականի փետրվարին 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

Chromosome in situ suppression hybridisation in human male meiosis.

@ast

Chromosome in situ suppression hybridisation in human male meiosis.

@en

type

label

Chromosome in situ suppression hybridisation in human male meiosis.

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Chromosome in situ suppression hybridisation in human male meiosis.

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prefLabel

Chromosome in situ suppression hybridisation in human male meiosis.

@ast

Chromosome in situ suppression hybridisation in human male meiosis.

@en

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P1433

Journal of Medical Genetics

P1476

Chromosome in situ suppression hybridisation in human male meiosis.

@en

P2093

Goldman AS

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Hultén MA

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P2860

Detection of chromosome aberrations in metaphase and interphase tumor cells by in situ hybridization using chromosome-specific library probes

Reproducible compartmentalization of individual chromosome domains in human CNS cells revealed by in situ hybridization and three-dimensional reconstruction

Cytogenetic analysis using quantitative, high-sensitivity, fluorescence hybridization

Fluorescence in situ hybridization with human chromosome-specific libraries: detection of trisomy 21 and translocations of chromosome 4.

Rapid metaphase and interphase detection of radiation-induced chromosome aberrations in human lymphocytes by chromosomal suppression in situ hybridization.

Construction of gene libraries for each human chromosome.

Chromosomal in situ suppression hybridization of human gonosomes and autosomes and its use in clinical cytogenetics.

Delineation of individual human chromosomes in metaphase and interphase cells by in situ suppression hybridization using recombinant DNA libraries.

Construction of fifteen human chromosome-specific DNA libraries from flow-purified chromosomes.

Direct nonradioactive in situ hybridization of somatic cell hybrid DNA to human lymphocyte chromosomes.

P304

98-102

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scholarly article

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10.1136/JMG.29.2.98

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2

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1613773

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