(Q38463893)

3 September 2017

Array painting using microdissected chromosomes to map chromosomal breakpoints (English)

1 reference

3 September 2017

Backx L

1

1 reference

3 September 2017

Van Esch H

2

1 reference

3 September 2017

Melotte C

3

1 reference

3 September 2017

Kosyakova N

4

1 reference

3 September 2017

Starke H

5

1 reference

3 September 2017

Frijns JP

6

1 reference

3 September 2017

Liehr T

7

1 reference

3 September 2017

Vermeesch JR

8

1 reference

3 September 2017

1 January 2007

1 reference

Cytogenetics and Genome Research

3 September 2017

1 reference

3 September 2017

116

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3 September 2017

158-166

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3 September 2017

3

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Oligophrenin-1 encodes a rhoGAP protein involved in X-linked mental retardation

3 September 2017

1 reference

Reverse painting highlights the origin of chromosome aberrations

21 January 2018

1 reference

A cryptic deletion of 2q35 including part of the PAX3 gene detected by breakpoint mapping in a child with autism and a de novo 2;8 translocation

21 January 2018

1 reference

Genomic profiling by DNA amplification of laser capture microdissected tissues and array CGH

21 January 2018

1 reference

Measurement and purification of human chromosomes by flow cytometry and sorting

21 January 2018

1 reference

Identification of a 650 kb duplication at the X chromosome breakpoint in a patient with 46,X,t(X;8)(q28;q12) and non-syndromic mental retardation

21 January 2018

1 reference

Delineation of the critical deletion region for congenital heart defects, on chromosome 8p23.1.

21 January 2018

1 reference

DNA microarrays for comparative genomic hybridization based on DOP-PCR amplification of BAC and PAC clones

21 January 2018

1 reference

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

21 January 2018

1 reference

Applications of combined DNA microarray and chromosome sorting technologies

21 January 2018

1 reference

The complex nature of constitutional de novo apparently balanced translocations in patients presenting with abnormal phenotypes

21 January 2018

1 reference

Rapid generation of region-specific genomic clones by chromosome microdissection: isolation of DNA from a region frequently deleted in malignant melanoma.

21 January 2018

1 reference

Current developments in human molecular cytogenetic techniques

21 January 2018

1 reference

Small supernumerary marker chromosomes (sSMC) in humans

21 January 2018

1 reference

Small supernumerary marker chromosomes – progress towards a genotype-phenotype correlation

21 January 2018

1 reference

Representational oligonucleotide microarray analysis: a high-resolution method to detect genome copy number variation

21 January 2018

1 reference

Cloning defined regions of the human genome by microdissection of banded chromosomes and enzymatic amplification

21 January 2018

1 reference

Paint-assisted microdissection-FISH: Rapid and simple mapping of translocation breakpoints in the embryonal rhabdomyosarcoma cell line RD.

21 January 2018

1 reference

Molecular breakpoint cloning and gene expression studies of a novel translocation t(4;15)(q27;q11.2) associated with Prader-Willi syndrome

21 January 2018

1 reference

Microdissection of banded human chromosomes

21 January 2018

1 reference

GATA3 haplo-insufficiency causes human HDR syndrome

21 January 2018

1 reference

Molecular karyotyping: array CGH quality criteria for constitutional genetic diagnosis.

21 January 2018

1 reference

Highly comprehensive karyotype analysis by a combination of spectral karyotyping (SKY), microdissection, and reverse painting (SKY-MD).

21 January 2018

1 reference

Degenerate oligonucleotide-primed PCR: General amplification of target DNA by a single degenerate primer

21 January 2018

1 reference

21 January 2018

Identifiers

DOI

10.1159/000098181

1 reference

3 September 2017

1 reference