(Q34146321)

31 July 2017

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

1 reference

31 July 2017

L Edelmann

1

1 reference

31 July 2017

E Spiteri

2

1 reference

31 July 2017

N McCain

3

1 reference

31 July 2017

R Goldberg

4

1 reference

31 July 2017

R K Pandita

5

1 reference

31 July 2017

S Duong

6

1 reference

31 July 2017

J Fox

7

1 reference

31 July 2017

D Blumenthal

8

1 reference

31 July 2017

S R Lalani

9

1 reference

31 July 2017

L G Shaffer

10

1 reference

31 July 2017

B E Morrow

11

1 reference

31 July 2017

language of work or name

English

0 references

publication date

1 December 1999

1 reference

American Journal of Human Genetics

31 July 2017

1 reference

31 July 2017

65

1 reference

31 July 2017

1608-1616

1 reference

31 July 2017

6

1 reference

A common molecular basis for rearrangement disorders on chromosome 22q11

31 July 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1288371

Low-copy repeats mediate the common 3-Mb deletion in patients with velo-cardio-facial syndrome.

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1288371

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

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1288371

Comparative sequence analysis of human minisatellites showing meiotic repeat instability.

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1288371

Fragile sites-cytogenetic similarity with molecular diversity

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1288371

Localization of Jacobsen syndrome breakpoints on a 40-Mb physical map of distal chromosome 11q

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1288371

A non-hypervariable human minisatellite strongly stimulates in vitro intramolecular homologous recombination

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1288371

Molecular definition of 22q11 deletions in 151 velo-cardio-facial syndrome patients

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1288371

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=1288371

Human chromosomal fragile site FRA16B is an amplified AT-rich minisatellite repeat

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1288371

Binding of zinc finger protein ZPR1 to the epidermal growth factor receptor

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1288371

Molecular characterization of de novo secondary trisomy 13.

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1288371

Molecular characterization of the marker chromosome associated with cat eye syndrome

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1288371

Molecular definition of the 22q11 deletions in velo-cardio-facial syndrome

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1288371

Minute supernumerary ring chromosome 22 associated with cat eye syndrome: further delineation of the critical region.

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1288371

Association of a chromosome deletion syndrome with a fragile site within the proto-oncogene CBL2

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1288371

The molecular basis of fragile sites in human chromosomes

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1288371

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=1288371

Chromosome translocations in couples with multiple spontaneous abortions

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1288371

Apolipoprotein multigene family: tandem organization of human apolipoprotein AI, CIII, and AIV genes

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1288371

The fragile site (16) (q22). I. Induction by AT-specific DNA-ligands and population frequency

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1288371

De novo balanced chromosome rearrangements and extra marker chromosomes identified at prenatal diagnosis: clinical significance and distribution of breakpoints

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1288371

Hypervariable polymorphism in the APOC3 gene

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1288371

High level of unequal meiotic crossovers at the origin of the 22q11. 2 and 7q11.23 deletions.

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1288371

Role of chromosome aberrations in recurrent abortion: a study of 269 balanced translocations

28 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1288371

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

28 October 2018

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

Tandem duplication of proximal 22q: a cause of cat-eye syndrome

1 reference

12 December 2020

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

1 reference

12 December 2020

Repeat unit sequence variation in minisatellites: a novel source of DNA polymorphism for studying variation and mutation by single molecule analysis

1 reference

12 December 2020

Genetic linkage of the human apolipoprotein AI-CIII-AIV gene cluster and the neural cell adhesion molecule (NCAM) gene

1 reference

12 December 2020

Isolation of the human chromosome 22q telomere and its application to detection of cryptic chromosomal abnormalities

1 reference

12 December 2020

Evidence for two distinct tumor-suppressor gene loci on the long arm of chromosome 11 in human oral cancer

1 reference

12 December 2020

Loss of heterozygosity at 11q23.1 in breast carcinomas: indication for involvement of a gene distal and close to ATM

1 reference

12 December 2020

Most Jacobsen syndrome deletion breakpoints occur distal to FRA11B

1 reference

12 December 2020

Cat eye syndrome chromosome breakpoint clustering: identification of two intervals also associated with 22q11 deletion syndrome breakpoints

1 reference

12 December 2020

High-resolution mapping of crossovers in human sperm defines a minisatellite-associated recombination hotspot

1 reference

12 December 2020

Chromosome 11q22.3-q25 LOH in ovarian cancer: association with a more aggressive disease course and involved subregions

1 reference

12 December 2020

Refined mapping of two regions of loss of heterozygosity on chromosome band 11q23 in lung cancer

1 reference

12 December 2020

Identifiers

DOI

10.1086/302689

1 reference

31 July 2017

1 reference

31 July 2017

1 reference