(Q33608623)

English

A unique case of der(11)t(11;22),-22 arising from 3:1 segregation of a maternal t(11;22) in a family with co-segregation of the translocation and breast cancer

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scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

28 July 2017

A unique case of der(11)t(11;22),-22 arising from 3:1 segregation of a maternal t(11;22) in a family with co-segregation of the translocation and breast cancer (English)

1 reference

Europe PubMed Central

PubMed publication ID

28 July 2017

Dorothy Warburton

5

object named as

Dorothy Warburton

1 reference

Europe PubMed Central

PubMed publication ID

28 July 2017

author name string

Vaidehi Jobanputra

1

1 reference

Europe PubMed Central

PubMed publication ID

28 July 2017

Wendy K Chung

2

1 reference

Europe PubMed Central

PubMed publication ID

28 July 2017

April M Hacker

3

1 reference

Europe PubMed Central

PubMed publication ID

28 July 2017

Beverly S Emanuel

4

1 reference

Europe PubMed Central

PubMed publication ID

28 July 2017

publication date

1 August 2005

1 reference

Europe PubMed Central

PubMed publication ID

28 July 2017

Prenatal Diagnosis

1 reference

Europe PubMed Central

PubMed publication ID

28 July 2017

25

1 reference

Europe PubMed Central

PubMed publication ID

28 July 2017

8

1 reference

Europe PubMed Central

PubMed publication ID

28 July 2017

683-686

1 reference

Europe PubMed Central

PubMed publication ID

28 July 2017

Cruciform DNA structure underlies the etiology for palindrome-mediated human chromosomal translocations

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2810961

21 June 2018

A palindrome-mediated mechanism distinguishes translocations involving LCR-B of chromosome 22q11.2

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2810961

21 June 2018

Unusual mosaic karyotype resulting from adjacent 1 segregation of t(11;22): importance of performing skin fibroblast karyotype in patients with unexplained multiple congenital anomalies

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2810961

21 June 2018

AT-rich palindromes mediate the constitutional t(11;22) translocation.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2810961

21 June 2018

Meiotic studies of a human male carrier of the common translocation, t(11;22), suggests postzygotic selection rather than preferential 3:1 MI segregation as the cause of liveborn offspring with an unbalanced translocation.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2810961

21 June 2018

Tightly clustered 11q23 and 22q11 breakpoints permit PCR-based detection of the recurrent constitutional t(11;22).

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2810961

21 June 2018

A common breakpoint on 11q23 in carriers of the constitutional t(11;22) translocation

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2810961

21 June 2018

Clustered 11q23 and 22q11 breakpoints and 3:1 meiotic malsegregation in multiple unrelated t(11;22) families

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2810961

21 June 2018

Preimplantation genetic diagnosis and sperm analysis by fluorescence in-situ hybridization for the most common reciprocal translocation t(11;22).

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2810961

21 June 2018

Der(22) syndrome and velo-cardio-facial syndrome/DiGeorge syndrome share a 1.5-Mb region of overlap on chromosome 22q11

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2810961

21 June 2018

Der(22)t(11;22) resulting from a paternal de novo translocation, adjacent 1 segregation, and maternal heterodisomy of chromosome 22.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2810961

21 June 2018

Predisposition for breast cancer in carriers of constitutional translocation 11q;22q

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2810961

21 June 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2810961

21 June 2018

Risks of unbalanced progeny at amniocentesis to carriers of chromosome rearrangements: data from United States and Canadian laboratories

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2810961

21 June 2018

The unbalanced offspring of the male carriers of the 11q;22q translocation: nondisjunction at meiosis II in a balanced spermatocyte.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2810961

21 June 2018

11Q;22Q translocation: Third case of imbalance not due to 3:1 nondisjunction in first meiosis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2810961

21 June 2018

Regions of genomic instability on 22q11 and 11q23 as the etiology for the recurrent constitutional t(11;22).

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2810961

30 October 2018

Long AT-rich palindromes and the constitutional t(11;22) breakpoint

1 reference

https://pubmed.ncbi.nlm.nih.gov/16049998

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/16049998

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/16049998

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Analysis of human sperm chromosome complements from a male heterozygous for a reciprocal translocation t(11;22)(q23;q11)

1 reference

https://pubmed.ncbi.nlm.nih.gov/16049998

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Congenital heart disease in supernumerary der(22),t(11;22) syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/16049998

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Not all chromosome imbalance resulting from the 11q;22q translocation is due to 3:1 segregation in first meiosis

1 reference

https://pubmed.ncbi.nlm.nih.gov/16049998

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Unusual segregation of constitutional 11q;22q translocation may be explained by crossover in interchange segment, followed by 3:1 segregation at meiosis I

1 reference

https://pubmed.ncbi.nlm.nih.gov/16049998

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The translocation 11q;22q: a novel unbalanced karyotype

1 reference

https://pubmed.ncbi.nlm.nih.gov/16049998

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Unusual segregation for 11q;22q parental translocation in a triplet pregnancy: prenatal diagnosis in chorionic villi and amniotic fluid

1 reference

https://pubmed.ncbi.nlm.nih.gov/16049998

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Unusual segregation of t(11;22) resulting from crossing-over followed by 3:1 disjunction at meiosis I

1 reference

https://pubmed.ncbi.nlm.nih.gov/16049998

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Multicolor fluorescence in situ hybridization analysis of the spermatozoa of a male heterozygous for a reciprocal translocation t(11;22)(q23;q11)

1 reference

https://pubmed.ncbi.nlm.nih.gov/16049998

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1002/PD.1196

1 reference

Europe PubMed Central

PubMed publication ID

28 July 2017

PMC publication ID

1 reference

Europe PubMed Central

PubMed publication ID

28 July 2017

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

28 July 2017

ResearchGate publication ID

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