(Q34142712)

31 July 2017

0 references

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

1 reference

31 July 2017

H Kurahashi

1 reference

31 July 2017

T H Shaikh

1 reference

31 July 2017

E H Zackai

1 reference

31 July 2017

L Celle

1 reference

31 July 2017

D A Driscoll

1 reference

31 July 2017

M L Budarf

1 reference

31 July 2017

B S Emanuel

1 reference

31 July 2017

language of work or name

English

0 references

publication date

20 July 2000

1 reference

American Journal of Human Genetics

31 July 2017

published in

1 reference

31 July 2017

1 reference

31 July 2017

1 reference

31 July 2017

page(s)

763-768

1 reference

Chromosome 22-specific low copy repeats and the 22q11.2 deletion syndrome: genomic organization and deletion endpoint analysis

31 July 2017

cites work

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1287537

Molecular cloning of translocation breakpoints in a case of constitutional translocation t(11;22)(q23;q11) and preparation of probes for preimplantation genetic diagnosis

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1287537

The DNA sequence of human chromosome 22

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1287537

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

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1287537

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

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1287537

Palindrome Resolution and Recombination in the Mammalian Germ Line

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1287537

The second case of a t(17;22) in a family with neurofibromatosis type 1: sequence analysis of the breakpoint regions

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1287537

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

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1287537

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

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1287537

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

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1287537

Loss of heterozygosity in sporadic human breast carcinoma: a common region between 11q22 and 11q23.3.

28 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1287537

Loss of heterozygosity at 11q22-q23 in breast cancer

28 October 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/10903930

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

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

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/10903930

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1086/303054

1 reference

31 July 2017

1 reference

31 July 2017

1 reference