(Q33678480)

28 July 2017

Familial complex chromosome rearrangement ascertained by in situ hybridisation (English)

1 reference

28 July 2017

Fuster C

1

1 reference

28 July 2017

Miguez L

2

1 reference

28 July 2017

Miró R

3

1 reference

28 July 2017

Rigola MA

4

1 reference

28 July 2017

Perez A

5

1 reference

28 July 2017

Egozcue J

6

1 reference

28 July 2017

language of work or name

English

0 references

publication date

1 February 1997

1 reference

Journal of Medical Genetics

28 July 2017

1 reference

28 July 2017

34

1 reference

28 July 2017

2

1 reference

28 July 2017

164-166

1 reference

The origin of cytologically unidentifiable chromosome abnormalities: six cases ascertained by targeted chromosome-band painting.

28 July 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1050874

Clarification of subtle reciprocal rearrangements using fluorescence in situ hybridization

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1050874

11q trisomy detected by fluorescence in situ hybridization

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1050874

A proposed system for scoring structural aberrations detected by chromosome painting

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1050874

Complex chromosomal rearrangements: some breakpoints may have cellular adaptive significance

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1050874

On the scoring of FISH-"painted" chromosome-type exchange aberrations

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1050874

Application of molecular and cytogenetic techniques to the detection of a de novo unbalanced t(11q;21q) in a patient previously diagnosed as having monosomy 21.

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1050874

Site-specific reciprocal translocation, t(11;22) (q23;q11), in several unrelated families with 3:1 meiotic disjunction

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1050874

Complex chromosomal rearrangements (CCR) and their genetic consequences.

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1050874

Complex chromosomal rearrangement in a woman with multiple miscarriages

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1050874

Confirmation of a balanced chromosomal translocation using molecular techniques

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1050874

Reassessment of two apparent deletions of chromosome 16p to an ins(11;16) and a t(1;16) by chromosome painting

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1050874

Trisomy 12 in chronic lymphocytic leukemia: an interphase cytogenetic study.

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1050874

Detection of subtle reciprocal translocations by fluorescence in situ hybridization

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1050874

De novo complex chromosome rearrangement in identical twins with multiple congenital anomalies

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1050874

The 11q;22q translocation: a European collaborative analysis of 43 cases

21 June 2018

1 reference

12 December 2020

Prenatal diagnosis of partial trisomy through in situ hybridization on amniocytes with whole chromosome and centromere-specific DNA probes. A case report

1 reference

12 December 2020

Incomplete trisomy 22. I. Familial 11/22 translocation with 3:1 meiotic disjunction. Delineation of a common clinical picture and report of nine new cases from six families

1 reference

12 December 2020

The 11q;22q translocation: a collaborative study of 20 new cases and analysis of 110 families

1 reference

12 December 2020

[Diagnosis of minor chromosome modifications by molecular cytogenetics]

1 reference

12 December 2020

Application of fluorescent in situ hybridization for 'de novo' anomalies in prenatal diagnosis

1 reference

12 December 2020

Balanced complex chromosome rearrangement ascertained through prenatal diagnosis

1 reference

12 December 2020

Fetal translocation between chromosomes 2, 18, and 21 resolved by fish

1 reference

12 December 2020

Identifiers

DOI

10.1136/JMG.34.2.164

1 reference

release_obraz3livfbrfijkrdigdyx6ai

28 July 2017

1 reference

Fatcat

https://api.fatcat.wiki/v0/release/obraz3livfbrfijkrdigdyx6ai

24 November 2022

mapped directly with Wikidata item

PMCID

1050874

1 reference

28 July 2017

1 reference