Heteromorphic variants of chromosome 9

Item

http://www.wikidata.org/entity/Q36767578

description

2013 nî lūn-bûn

@nan

2013年の論文

@ja

2013年論文

@yue

2013年論文

@zh-hant

2013年論文

@zh-hk

2013年論文

@zh-mo

2013年論文

@zh-tw

2013年论文

@wuu

2013年论文

@zh

2013年论文

@zh-cn

name

Heteromorphic variants of chromosome 9

@ast

Heteromorphic variants of chromosome 9

@en

type

Item

label

Heteromorphic variants of chromosome 9

@ast

Heteromorphic variants of chromosome 9

@en

prefLabel

Heteromorphic variants of chromosome 9

@ast

Heteromorphic variants of chromosome 9

@en

P1476

Heteromorphic variants of chromosome 9

@en

P2093

Ali Sazci

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Alla Frolova

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Ani Grigorian

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Anja Weise

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Anna D Polityko

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Anna I Kulpanovich

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Emel Ergul

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Evgenia Jaroshevich

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Gisela Reising-Ackermann

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Hasmik Mkrtchyan

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P2860

Sperm DNA integrity and meiotic behavior assessment in an infertile male carrier of a 9qh+++ polymorphism.

Molecular topography of the secondary constriction region (qh) of human chromosome 9 with an unusual euchromatic band.

A new multicolor fluorescence in situ hybridization probe set directed against human heterochromatin: HCM-FISH.

Thirty-two new cases with small supernumerary marker chromosomes detected in connection with fertility problems: detailed molecular cytogenetic characterization and review of the literature.

The euchromatic 9p+ polymorphism is a locus-specific amplification caused by repeated copies of a small DNA segment mapping within 9p12.

Complete deficiency of constitutive heterochromatin on a human chromosome 9.

Global screening and extended nomenclature for 230 aphidicolin-inducible fragile sites, including 61 yet unreported ones.

Novel deletion variants of 9q13-q21.12 and classical euchromatic variants of 9q12/qh involve deletion, duplication and triplication of large tracts of segmentally duplicated pericentromeric euchromatin.

Breakpoints in alpha, beta, and satellite III DNA sequences of chromosome 9 result in a variety of pericentric inversions.

A case-control study identifying chromosomal polymorphic variations as forms of epigenetic alterations associated with the infertility phenotype.

P2888

1755-8166-6-14

P304

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P31

scholarly article

P356

10.1186/1755-8166-6-14

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P433

http://www.w3.org/2001/XMLSchema#string

P478

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P577

2013-04-01T00:00:00Z

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P5875

236098817

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P698

23547710

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P932

3626942

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