Fine mapping of an imprinted gene for familial nonchromaffin paragangliomas, on chromosome 11q23. (Q34412277)

2 August 2017

Fine mapping of an imprinted gene for familial nonchromaffin paragangliomas, on chromosome 11q23. (English)

1 reference

2 August 2017

B E Baysal

1

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2 August 2017

J E Farr

2

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2 August 2017

W S Rubinstein

3

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2 August 2017

R A Galus

4

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2 August 2017

K A Johnson

5

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2 August 2017

C E Aston

6

1 reference

2 August 2017

E N Myers

7

1 reference

2 August 2017

J T Johnson

8

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2 August 2017

R Carrau

9

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2 August 2017

S J Kirkpatrick

10

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2 August 2017

D Myssiorek

11

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2 August 2017

D Singh

12

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2 August 2017

S Saha

13

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2 August 2017

S M Gollin

14

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2 August 2017

G A Evans

15

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2 August 2017

M R James

16

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2 August 2017

C W Richard

17

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2 August 2017

language of work or name

English

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publication date

1 January 1997

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American Journal of Human Genetics

2 August 2017

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2 August 2017

60

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2 August 2017

1

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2 August 2017

121-132

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Localization of a tumor suppressor gene in 11p15.5 using the G401 Wilms' tumor assay

2 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1712548

Multiple genetic loci within 11p15 defined by Beckwith-Wiedemann syndrome rearrangement breakpoints and subchromosomal transferable fragments

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1712548

A comprehensive genetic map of the human genome based on 5,264 microsatellites

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1712548

Tumor cell growth arrest caused by subchromosomal transferable DNA fragments from chromosome 11

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1712548

Loss of heterozygosity and amplification on chromosome 11q in human ovarian cancer

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1712548

Loss of heterozygosity in cervical carcinoma: subchromosomal localization of a putative tumor-suppressor gene to chromosome 11q22-q24

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1712548

A radiation hybrid map of 506 STS markers spanning human chromosome 11.

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1712548

Parental origin effects, genome imprinting, and sex-ratio distortion: double or nothing?

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1712548

Familial paragangliomas of the head and neck

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1712548

Fine mapping of a putatively imprinted gene for familial non-chromaffin paragangliomas to chromosome 11q13.1: evidence for genetic heterogeneity

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1712548

A defined region of loss of heterozygosity at 11q23 in cutaneous malignant melanoma.

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1712548

Parents do matter: genomic imprinting and parental sex effects in neurological disorders.

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1712548

CpNpG methylation in mammalian cells

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1712548

Gametic imprinting in mammals

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1712548

The VITESSE algorithm for rapid exact multilocus linkage analysis via genotype set-recoding and fuzzy inheritance

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1712548

Familial carotid body tumors: case report and epidemiologic review

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1712548

Carotid body tumors in humans: genetics and epidemiology

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1712548

6 July 2018

Genetics of human cancer

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1712548

Anticipation in myotonic dystrophy: fact or fiction?

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1712548

Genomic imprinting in hereditary glomus tumours: evidence for new genetic theory

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1712548

Allelotype of colorectal carcinomas

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1712548

Premeiotic instability of repeated sequences in Neurospora crassa

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1712548

Anticipation in myotonic dystrophy. I. Statistical verification based on clinical and haplotype findings

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1712548

DNA methylation represses FMR-1 transcription in fragile X syndrome

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1712548

A gene subject to genomic imprinting and responsible for hereditary paragangliomas maps to chromosome 11q23-qter

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1712548

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

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1712548

Statistical pitfalls in detecting age-of-onset anticipation: the role of correlation in studying anticipation and detecting ascertainment bias

27 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1712548

Deletion mapping of chromosome 11 in carcinoma of the bladder.

27 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1712548

Analysis of a second family with hereditary non-chromaffin paragangliomas locates the underlying gene at the proximal region of chromosome 11q

27 October 2018

1 reference

12 December 2020

Loss of heterozygosity in malignant melanoma at loci on chromosomes 11 and 17 implicated in the pathogenesis of other cancers

1 reference

12 December 2020

Deletion of chromosome 11 and of 14q sequences in neuroblastoma

1 reference

12 December 2020

Is there evidence for anticipation in autosomal-dominant polycystic kidney disease?

1 reference

12 December 2020

Loss of imprinting of IGF2 is linked to reduced expression and abnormal methylation of H19 in Wilms' tumour

1 reference

12 December 2020

Epigenetic lesions at the H19 locus in Wilms' tumour patients

1 reference

12 December 2020

Familial chemodectoma

1 reference

12 December 2020

Allelotype of head and neck paragangliomas: Allelic imbalance is confined to the long arm of chromosome 11, the site of the predisposing locusPGL

1 reference

12 December 2020

Further localization of the gene for hereditary paragangliomas and evidence for linkage in unrelated families

1 reference

12 December 2020

Allelic losses in human chromosome 11 in lung cancers

1 reference

12 December 2020

Definition and refinement of chromosome 11 regions of loss of heterozygosity in breast cancer: identification of a new region at 11q23.3.

1 reference

12 December 2020

HEREDITARY DEFICIENCIES OF CLOTTING FACTORS VII AND X ASSOCIATED WITH CAROTID-BODY TUMORS

1 reference

12 December 2020

Inheritance of glomus tumours

1 reference

12 December 2020

Parental-specific methylation of an imprinted transgene is established during gametogenesis and progressively changes during embryogenesis

1 reference

12 December 2020

11q deletions in human colorectal carcinomas: Cytogenetics and restriction fragment length polymorphism analysis

1 reference

12 December 2020

Identifiers

PMCID

1712548

1 reference

2 August 2017

1 reference