Microarray-based genome investigation: molecular karyotyping or segmental aneuploidy profiling? (Q82162970)

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15 January 2020

title

Microarray-based genome investigation: molecular karyotyping or segmental aneuploidy profiling? (English)

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15 January 2020

author name string

Ron Hochstenbach

series ordinal

1

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15 January 2020

Hans Kristian Ploos van Amstel

series ordinal

2

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15 January 2020

Martin Poot

series ordinal

3

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15 January 2020

publication date

1 March 2006

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European Journal of Human Genetics

15 January 2020

published in

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15 January 2020

volume

14

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15 January 2020

issue

3

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15 January 2020

page(s)

262-265

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https://scigraph.springernature.com/pub.10.1038/sj.ejhg.5201553

15 January 2020

exact match

0 references

cites work

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Molecular karyotyping using an SNP array for genomewide genotyping.

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Microarray analysis of cell-free fetal DNA in amniotic fluid: a prenatal molecular karyotype.

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Molecular karyotyping in human constitutional cytogenetics

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Array painting: a method for the rapid analysis of aberrant chromosomes using DNA microarrays

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The molecular karyotype of Leishmania major and mapping of alpha and beta tubulin gene families to multiple unlinked chromosomal loci

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7 January 2021

Trypanosoma cruzi exhibits inter- and intra-strain heterogeneity in molecular karyotype and chromosomal gene location

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7 January 2021

Molecular karyotype of Plasmodium falciparum: conserved linkage groups and expendable histidine-rich protein genes

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7 January 2021

A refined molecular karyotype for the reference strain of the Trypanosoma cruzi genome project (clone CL Brener) by assignment of chromosome markers

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7 January 2021

High-resolution analysis of human peripheral lymphocyte chromosomes by flow cytometry

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7 January 2021

Direct hybridization of sorted human chromosomes: localization of the Y chromosome on the flow karyotype

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7 January 2021

Gene mapping by chromosome spot hybridization

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7 January 2021

Detection of large-scale variation in the human genome

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7 January 2021

Large-scale copy number polymorphism in the human genome

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7 January 2021

Segmental duplications and copy-number variation in the human genome

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7 January 2021

Genomic segmental polymorphisms in inbred mouse strains

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7 January 2021

Complex haplotypes, copy number polymorphisms and coding variation in two recently divergent mouse strains

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7 January 2021

Supernumerary ring chromosome 7 mosaicism: case report, investigation of the gene content, and delineation of the phenotype

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7 January 2021

Disruption of Netrin G1 by a balanced chromosome translocation in a girl with Rett syndrome.

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7 January 2021

Disruption of contactin 4 (CNTN4) results in developmental delay and other features of 3p deletion syndrome

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https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201553

7 January 2021

A candidate gene for congenital bilateral isolated ptosis identified by molecular analysis of a de novo balanced translocation

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7 January 2021

Mutations in the ZNF41 gene are associated with cognitive deficits: identification of a new candidate for X-linked mental retardation

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7 January 2021

Identifiers

DOI

10.1038/SJ.EJHG.5201553

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16391563%20AND%20SRC:MED&resulttype=core&format=json

15 January 2020

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