(Q30825198)

26 June 2017

Population data suggest that deletions of 1p36 are a relatively common chromosome abnormality (English)

1 reference

26 June 2017

Heilstedt HA

1

1 reference

26 June 2017

Ballif BC

2

1 reference

26 June 2017

Howard LA

3

1 reference

26 June 2017

Kashork CD

4

1 reference

26 June 2017

Shaffer LG

5

1 reference

26 June 2017

1 October 2003

1 reference

26 June 2017

1 reference

26 June 2017

64

1 reference

26 June 2017

4

1 reference

26 June 2017

310-316

1 reference

The promise and pitfalls of telomere region-specific probes

26 June 2017

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2003.00126.X

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2003.00126.X

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2003.00126.X

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2003.00126.X

7 January 2021

The detection of subtelomeric chromosomal rearrangements in idiopathic mental retardation

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2003.00126.X

7 January 2021

How microsatellite analysis can be exploited for subtelomeric chromosomal rearrangement analysis in mental retardation

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2003.00126.X

7 January 2021

Scanning for telomeric deletions and duplications and uniparental disomy using genetic markers in 120 children with malformations.

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2003.00126.X

7 January 2021

A novel automated strategy for screening cryptic telomeric rearrangements in children with idiopathic mental retardation.

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2003.00126.X

7 January 2021

Automated fluorescent genotyping detects 10% of cryptic subtelomeric rearrangements in idiopathic syndromic mental retardation.

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2003.00126.X

7 January 2021

Subtle chromosomal rearrangements in children with unexplained mental retardation

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2003.00126.X

7 January 2021

Screening for subtelomeric chromosome abnormalities in children with idiopathic mental retardation using multiprobe telomeric FISH and the new MAPH telomeric assay.

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2003.00126.X

7 January 2021

Subtelomeric rearrangements: results from a study of selected and unselected probands with idiopathic mental retardation and control individuals by using high-resolution G-banding and FISH.

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2003.00126.X

7 January 2021

Detection of submicroscopic aberrations in patients with unexplained mental retardation by fluorescence in situ hybridization using multiple subtelomeric probes.

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2003.00126.X

7 January 2021

Cryptic telomeric rearrangements in subjects with mental retardation associated with dysmorphism and congenital malformations

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2003.00126.X

7 January 2021

Submicroscopic terminal deletions and duplications in retarded patients with unclassified malformation syndromes.

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2003.00126.X

7 January 2021

Study of 250 children with idiopathic mental retardation reveals nine cryptic and diverse subtelomeric chromosome anomalies.

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2003.00126.X

7 January 2021

Detecting rearrangements in children using subtelomeric FISH and SKY.

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2003.00126.X

7 January 2021

Subtelomeric rearrangements detected in patients with idiopathic mental retardation

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2003.00126.X

7 January 2021

Comparative genomic hybridisation in mentally retarded patients with dysmorphic features and a normal karyotype.

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2003.00126.X

7 January 2021

Paternal origin of the de novo deleted chromosome 4 in Wolf-Hirschhorn syndrome

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2003.00126.X

7 January 2021

Parental origin of chromosome 4p deletion in Wolf-Hirschhorn syndrome

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2003.00126.X

7 January 2021

Paternal origin of the chromosomal deletion resulting in Wolf-Hirschhorn syndrome

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2003.00126.X

7 January 2021

Effect of the size of the deletion and clinical manifestation in Wolf-Hirschhorn syndrome: analysis of 13 patients with a de novo deletion

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2003.00126.X

7 January 2021

Parental origin of chromosome 5 deletions in the cri-du-chat syndrome

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2003.00126.X

7 January 2021

Partial monosomy of the short arm of chromosome 9: a distinct clinical entity

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2003.00126.X

7 January 2021

Parental origin of De Novo chromosome 9 deletions in del(9p) syndrome

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2003.00126.X

7 January 2021

Most Jacobsen syndrome deletion breakpoints occur distal to FRA11B

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2003.00126.X

7 January 2021

Further delineation of the chromosome 14q terminal deletion syndrome

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2003.00126.X

7 January 2021

Stable length polymorphism of up to 260 kb at the tip of the short arm of human chromosome 16

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2003.00126.X

7 January 2021

Analysis of clinical variation seen in patients with 18q terminal deletions

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2003.00126.X

7 January 2021

Preferential loss of the paternal alleles in the 18q- syndrome

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2003.00126.X

7 January 2021

Deletion mapping by FISH with BACs in patients with partial monosomy 22q13.

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2003.00126.X

7 January 2021

Two 22q telomere deletions serendipitously detected by FISH

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2003.00126.X

7 January 2021

The Wolf-Hirschhorn syndrome. I. Genetics.

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2003.00126.X

7 January 2021

The Cri du Chat syndrome: epidemiology, cytogenetics, and clinical features

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2003.00126.X

7 January 2021

Clinical and molecular characterisation of 80 patients with 5p deletion: genotype-phenotype correlation

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2003.00126.X

7 January 2021

Molecular characterization of 18p deletions: evidence for a breakpoint cluster

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2003.00126.X

7 January 2021

10.1034/J.1399-0004.2003.00126.X

Identifiers

DOI

1 reference

26 June 2017

1 reference