(Q33904701)

29 July 2017

Physical map of 1p36, placement of breakpoints in monosomy 1p36, and clinical characterization of the syndrome (English)

1 reference

29 July 2017

7

Carlos A Bacino

1 reference

29 July 2017

Heidi A Heilstedt

1

1 reference

29 July 2017

Blake C Ballif

2

1 reference

29 July 2017

Leslie A Howard

3

1 reference

29 July 2017

Richard A Lewis

4

1 reference

29 July 2017

Samuel Stal

5

1 reference

29 July 2017

Catherine D Kashork

6

1 reference

29 July 2017

Stuart K Shapira

8

1 reference

29 July 2017

Lisa G Shaffer

9

1 reference

29 July 2017

language of work or name

English

0 references

publication date

8 April 2003

1 reference

American Journal of Human Genetics

29 July 2017

1 reference

29 July 2017

72

1 reference

29 July 2017

1200-1212

1 reference

29 July 2017

5

1 reference

Monosomy 1p36--a recently delineated, clinically recognizable syndrome

29 July 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1180272

Loss of the SKI proto-oncogene in individuals affected with 1p36 deletion syndrome is predicted by strain-dependent defects in Ski-/- mice

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1180272

Molecular mechanisms for constitutional chromosomal rearrangements in humans

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1180272

An optimized set of human telomere clones for studying telomere integrity and architecture.

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1180272

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1180272

A common molecular basis for rearrangement disorders 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=1180272

Homologous recombination of a flanking repeat gene cluster is a mechanism for a common contiguous gene deletion 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=1180272

Chromosome 1p36 deletions: the clinical phenotype and molecular characterization of a common newly delineated 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=1180272

Development and clinical application of an innovative fluorescence in situ hybridization technique which detects submicroscopic rearrangements involving telomeres

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1180272

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=1180272

A region of consistent deletion in neuroblastoma maps within human chromosome 1p36.2-36.3

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1180272

Chromosome 1p terminal deletion: report of new findings and confirmation of two characteristic phenotypes

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1180272

A highly conserved repetitive DNA sequence, (TTAGGG)n, present at the telomeres of 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=1180272

The highest gene concentrations in the human genome are in telomeric bands of metaphase 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=1180272

Terminal deletion of 1p36.

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1180272

Loss of the potassium channel beta-subunit gene, KCNAB2, is associated with epilepsy in patients with 1p36 deletion syndrome.

29 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1180272

FISHing for mechanisms of cytogenetically defined terminal deletions using chromosome-specific subtelomeric probes.

29 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1180272

The promise and pitfalls of telomere region-specific probes

29 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1180272

Molecular refinement of the 1p36 deletion syndrome reveals size diversity and a preponderance of maternally derived deletions.

29 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1180272

Sequence comparison of human and yeast telomeres identifies structurally distinct subtelomeric domains.

29 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1180272

Band 1p36 abnormalities and t(1;17) in ovarian carcinoma

29 October 2018

1 reference

12 December 2020

Abnormalities in the p34cdc2-related PITSLRE protein kinase gene complex (CDC2L) on chromosome band 1p36 in melanoma

1 reference

12 December 2020

Chromosome abnormalities in malignant melanoma: clinical significance of nonrandom chromosome abnormalities in 206 cases

1 reference

12 December 2020

Tumor suppressor genes on the short arm of chromosome 1 in neuroblastoma

1 reference

12 December 2020

Genetic syndromes and uniparental disomy: a study of 16 cases of Brachmann-de Lange syndrome.

1 reference

12 December 2020

Identifiers

DOI

10.1086/375179

1 reference

29 July 2017

1 reference

29 July 2017

1 reference