(Q35194082)

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A radiation hybrid map of the distal short arm of human chromosome 11, containing the Beckwith-Wiedemann and associated embryonal tumor disease loci

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Europe PubMed Central

PubMed publication ID

7 August 2017

A radiation hybrid map of the distal short arm of human chromosome 11, containing the Beckwith-Wiedemann and associated embryonal tumor disease loci (English)

1 reference

Europe PubMed Central

PubMed publication ID

7 August 2017

Michael Boehnke

2

object named as

M Boehnke

1 reference

Europe PubMed Central

PubMed publication ID

7 August 2017

author name string

C W Richard

1

1 reference

Europe PubMed Central

PubMed publication ID

7 August 2017

D J Berg

3

1 reference

Europe PubMed Central

PubMed publication ID

7 August 2017

J H Lichy

4

1 reference

Europe PubMed Central

PubMed publication ID

7 August 2017

T C Meeker

5

1 reference

Europe PubMed Central

PubMed publication ID

7 August 2017

E Hauser

6

1 reference

Europe PubMed Central

PubMed publication ID

7 August 2017

R M Myers

7

1 reference

Europe PubMed Central

PubMed publication ID

7 August 2017

D R Cox

8

1 reference

Europe PubMed Central

PubMed publication ID

7 August 2017

language of work or name

0 references

publication date

1 May 1993

1 reference

Europe PubMed Central

PubMed publication ID

7 August 2017

American Journal of Human Genetics

1 reference

Europe PubMed Central

PubMed publication ID

7 August 2017

52

1 reference

Europe PubMed Central

PubMed publication ID

7 August 2017

5

1 reference

Europe PubMed Central

PubMed publication ID

7 August 2017

915-921

1 reference

Europe PubMed Central

PubMed publication ID

7 August 2017

Abnormality of chromosome 11 in patients with features of Beckwith-Wiedemann syndrome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682045

13 July 2018

"A technique for radiolabeling DNA restriction endonuclease fragments to high specific activity". Addendum

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682045

13 July 2018

Analysis of human chromosome 11 by somatic cell genetics: reexamination of derivatives of human-hamster cell line J1.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682045

13 July 2018

The hemopexin gene maps to the same location as the beta-globin gene cluster on human chromosome 11

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682045

13 July 2018

Human tyrosine hydroxylase and insulin genes are contiguous on chromosome 11

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682045

13 July 2018

Alu polymerase chain reaction: a method for rapid isolation of human-specific sequences from complex DNA sources

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682045

13 July 2018

A fine-structure deletion map of human chromosome 11p: analysis of J1 series hybrids

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682045

13 July 2018

Tumor-specific loss of 11p15.5 alleles in del11p13 Wilms tumor and in familial adrenocortical carcinoma

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682045

13 July 2018

Genetic linkage of Beckwith-Wiedemann syndrome to 11p15.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682045

13 July 2018

Loss of allelic heterozygosity at a second locus on chromosome 11 in sporadic Wilms' tumor cells

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682045

13 July 2018

Familial Wiedemann-Beckwith syndrome and a second Wilms tumor locus both map to 11p15.5.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682045

13 July 2018

High-resolution mapping of human chromosome 11 by in situ hybridization with cosmid clones

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682045

13 July 2018

The placental ribonuclease inhibitor (RNH) gene is located on chromosome subband 11p15.5

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682045

13 July 2018

Molecular characterization of Beckwith-Wiedemann syndrome (BWS) patients with partial duplication of chromosome 11p excludes the gene MYOD1 from the BWS region

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682045

13 July 2018

Radiation hybrid mapping: a somatic cell genetic method for constructing high-resolution maps of mammalian chromosomes

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682045

13 July 2018

Vector-Alu PCR: a rapid step in mapping cosmids and YACs

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682045

13 July 2018

Loss of heterozygosity in Wilms' tumors, studied for six putative tumor suppressor regions, is limited to chromosome 11.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682045

13 July 2018

A panel of irradiation-reduced hybrids selectively retaining human chromosome 11p13: their structure and use to purify the WAGR gene complex

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682045

13 July 2018

A cloned DNA segment from the telomeric region of human chromosome 4p is not detectably rearranged in Huntington disease patients

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682045

13 July 2018

PCR primers for human chromosomes: reagents for the rapid analysis of somatic cell hybrids

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682045

13 July 2018

Regional assignment of the human acid sphingomyelinase gene (SMPD1) by PCR analysis of somatic cell hybrids and in situ hybridization to 11p15.1----p15.4

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682045

13 July 2018

Wee1+-like gene in human cells

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682045

13 July 2018

Statistical methods for multipoint radiation hybrid mapping

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682045

13 July 2018

Paternal origin of 11p15 duplications in the Beckwith-Wiedemann syndrome. A new case and review of the literature

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682045

13 July 2018

A radiation hybrid map of the proximal long arm of human chromosome 11 containing the multiple endocrine neoplasia type 1 (MEN-1) and bcl-1 disease loci.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682045

13 July 2018

Uniparental paternal disomy in a genetic cancer-predisposing syndrome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682045

13 July 2018

Identification of a human chromosome 11 gene which is differentially regulated in tumorigenic and nontumorigenic somatic cell hybrids of HeLa cells

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682045

13 July 2018

Monoallelic expression of the human H19 gene

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682045

13 July 2018

Mapping of 262 DNA markers into 24 intervals on human chromosome 11.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682045

13 July 2018

Physical linkage of two mammalian imprinted genes, H19 and insulin-like growth factor 2

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682045

13 July 2018

Trisomy 11p15 and Beckwith-Wiedemann syndrome. A report of two cases.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682045

27 September 2018

Trisomy 11p15 and Beckwith-Wiedemann syndrome. Report of two new cases

1 reference

https://pubmed.ncbi.nlm.nih.gov/8387721

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

An infant with Beckwith-Wiedemann syndrome and chromosomal duplication 11p13----pter.: correlation of symptoms between 11p trisomy and Beckwith-Wiedemann syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/8387721

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Molecular definition of the 11p15.5 region involved in Beckwith-Wiedemann syndrome and probably in predisposition to adrenocortical carcinoma

1 reference

https://pubmed.ncbi.nlm.nih.gov/8387721

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mitotic deletions of 11p15.5 in two different tumors indicate that the CALCA locus is distal to the PTH locus

1 reference

https://pubmed.ncbi.nlm.nih.gov/8387721

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A cosmid clone map derived from a small region of human chromosome 11

1 reference

https://pubmed.ncbi.nlm.nih.gov/8387721

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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PMC publication ID

1 reference

Europe PubMed Central

PubMed publication ID

7 August 2017

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

7 August 2017

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