Microdeletion syndromes disclose replication timing alterations of genes unrelated to the missing DNA. - Wikidata - awgldk - TriplyDB

Microdeletion syndromes disclose replication timing alterations of genes unrelated to the missing DNA.

Microdeletion syndromes disclose replication timing alterations of genes unrelated to the missing DNA.

http://www.wikidata.org/entity/Q37139251

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X-chromosome terminal deletion in a female with premature ovarian failure: Haploinsufficiency of X-linked genes as a possible explanation Ontogenetic variation of the human genome.

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Microdeletion syndromes disclose replication timing alterations of genes unrelated to the missing DNA.

http://www.wikidata.org/entity/Q37139251

description

article científic

@ca

article scientifique

@fr

articolo scientifico

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artigo científico

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bilimsel makale

@tr

scientific article published on 14 March 2009

@en

vedecký článok

@sk

vetenskaplig artikel

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videnskabelig artikel

@da

vědecký článek

@cs

name

Microdeletion syndromes disclo ...... unrelated to the missing DNA.

@en

Microdeletion syndromes disclo ...... unrelated to the missing DNA.

@nl

type

label

Microdeletion syndromes disclo ...... unrelated to the missing DNA.

@en

Microdeletion syndromes disclo ...... unrelated to the missing DNA.

@nl

prefLabel

Microdeletion syndromes disclo ...... unrelated to the missing DNA.

@en

Microdeletion syndromes disclo ...... unrelated to the missing DNA.

@nl

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Molecular Cytogenetics

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Microdeletion syndromes disclo ...... unrelated to the missing DNA.

@en

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Ayelet Rimon

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

Itay Amir

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

Jane Freedman

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

Josepha Yeshaya

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

Lydia Avivi

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

Mordechai Shohat

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

P2860

Structural variation in the human genome

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A common molecular basis for rearrangement disorders on chromosome 22q11

MeCP2 in neurons: closing in on the causes of Rett syndrome

Developmental regulation of DNA replication timing at the human beta globin locus.

The history of cancer epigenetics

To err (meiotically) is human: the genesis of human aneuploidy

FISH analysis of replication and transcription of chromosome X loci: new approach for genetic analysis of Rett syndrome.

Aberrant allele-specific replication, independent of parental origin, in blood cells of cancer patients.

The functional impact of structural variation in humans.

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11

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scholarly article

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10.1186/1755-8166-2-11

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2

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2009-03-14T00:00:00Z

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1041316655

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19284877

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