(Q83069838)

English

Breakpoint mapping and haplotype analysis of three reciprocal translocations identify a novel recurrent translocation in two unrelated families: t(4;11)(p16.2;p15.4)

scientific article published on 24 December 2008

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scholarly article

1 reference

Europe PubMed Central

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19 January 2020

Breakpoint mapping and haplotype analysis of three reciprocal translocations identify a novel recurrent translocation in two unrelated families: t(4;11)(p16.2;p15.4) (English)

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19104840%20AND%20SRC:MED&resulttype=core&format=json

19 January 2020

Katherine L Lachlan

6

1 reference

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19 January 2020

author name string

N Simon Thomas

1

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19 January 2020

Viv Maloney

2

1 reference

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19 January 2020

Victoria Bryant

3

1 reference

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19 January 2020

Shuwen Huang

4

1 reference

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19 January 2020

Carole Brewer

5

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19 January 2020

Patricia A Jacobs

7

1 reference

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19 January 2020

publication date

24 December 2008

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19 January 2020

1 reference

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19 January 2020

125

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19 January 2020

181-188

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19 January 2020

2

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19 January 2020

https://scigraph.springernature.com/pub.10.1007/s00439-008-0611-8

0 references

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/19104840

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A study of reciprocal translocations and inversions detected by light microscopy with special reference to origin, segregation, and recurrent abnormalities

1 reference

https://pubmed.ncbi.nlm.nih.gov/19104840

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Overlapping phenotype of Wolf-Hirschhorn and Beckwith-Wiedemann syndromes in a girl with der(4)t(4;11)(pter;pter).

1 reference

https://pubmed.ncbi.nlm.nih.gov/19104840

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Co-occurrence of 4p16.3 deletions with both paternal and maternal duplications of 11p15: modification of the Wolf-Hirschhorn syndrome phenotype by genetic alterations predicted to result in either a Beckwith-Wiedemann or Russell-Silver phenotype

1 reference

https://pubmed.ncbi.nlm.nih.gov/19104840

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Investigation of the origins of human autosomal inversions

1 reference

https://pubmed.ncbi.nlm.nih.gov/19104840

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A novel sequence-based approach to localize translocation breakpoints identifies the molecular basis of a t(4;22)

1 reference

https://pubmed.ncbi.nlm.nih.gov/19104840

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A collaborative study of the segregation of inherited chromosome structural rearrangements in 1356 prenatal diagnoses

1 reference

https://pubmed.ncbi.nlm.nih.gov/19104840

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

An 11p;17p telomeric translocation in two families associated with recurrent miscarriages and Miller-Dieker syndrome.

1 reference

https://pubmed.ncbi.nlm.nih.gov/19104840

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Heterozygous submicroscopic inversions involving olfactory receptor-gene clusters mediate the recurrent t(4;8)(p16;p23) translocation

1 reference

https://pubmed.ncbi.nlm.nih.gov/19104840

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Frequent translocations occur between low copy repeats on chromosome 22q11.2 (LCR22s) and telomeric bands of partner chromosomes.

1 reference

https://pubmed.ncbi.nlm.nih.gov/19104840

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Meiotic recombination and spatial proximity in the etiology of the recurrent t(11;22)

1 reference

https://pubmed.ncbi.nlm.nih.gov/19104840

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Systematic analysis of 95 reciprocal translocations of autosomes

1 reference

https://pubmed.ncbi.nlm.nih.gov/19104840

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identification of sequence motifs at the breakpoint junctions in three t(1;9)(p36.3;q34) and delineation of mechanisms involved in generating balanced translocations

1 reference

https://pubmed.ncbi.nlm.nih.gov/19104840

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Genome architecture catalyzes nonrecurrent chromosomal rearrangements

1 reference

https://pubmed.ncbi.nlm.nih.gov/19104840

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Molecular and genomic characterisation of cryptic chromosomal alterations leading to paternal duplication of the 11p15.5 Beckwith-Wiedemann region

1 reference

https://pubmed.ncbi.nlm.nih.gov/19104840

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/19104840

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The constitutional t(17;22): another translocation mediated by palindromic AT-rich repeats

1 reference

https://pubmed.ncbi.nlm.nih.gov/19104840

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/19104840

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Unbalanced translocation in a mother and her son in one of two 5;10 translocation families.

1 reference

https://pubmed.ncbi.nlm.nih.gov/19104840

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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