Unexpectedly high rate of de novo constitutional t(11;22) translocations in sperm from normal males (Q74592036)

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11 November 2019

title

Unexpectedly high rate of de novo constitutional t(11;22) translocations in sperm from normal males (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11586296%20AND%20SRC:MED&resulttype=core&format=json

11 November 2019

author name string

Kurahashi H

series ordinal

1

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11 November 2019

Emanuel BS

series ordinal

2

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11 November 2019

publication date

1 October 2001

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11 November 2019

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11 November 2019

volume

29

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11 November 2019

issue

2

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11 November 2019

page(s)

139-140

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https://scigraph.springernature.com/pub.10.1038/ng1001-139

11 November 2019

exact match

0 references

cites work

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

1 reference

https://api.crossref.org/works/10.1038%2FNG1001-139

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FNG1001-139

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FNG1001-139

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FNG1001-139

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FNG1001-139

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FNG1001-139

7 January 2021

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://api.crossref.org/works/10.1038%2FNG1001-139

7 January 2021

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://api.crossref.org/works/10.1038%2FNG1001-139

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FNG1001-139

7 January 2021

Frequent chromosomal translocations induced by DNA double-strand breaks

1 reference

https://api.crossref.org/works/10.1038%2FNG1001-139

7 January 2021

GT repeats are associated with recombination on human chromosome 22.

1 reference

https://api.crossref.org/works/10.1038%2FNG1001-139

7 January 2021

Long palindromic sequences induce double-strand breaks during meiosis in yeast.

1 reference

https://api.crossref.org/works/10.1038%2FNG1001-139

7 January 2021

Alu-mediated PCR artifacts and the constitutional t(11;22) breakpoint

1 reference

https://api.crossref.org/works/10.1038%2FNG1001-139

7 January 2021

Identifiers

DOI

10.1038/NG1001-139

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11586296%20AND%20SRC:MED&resulttype=core&format=json

11 November 2019

1 reference