Linkage analysis of a DNA marker localized to 20p12 and multiple endocrine neoplasia type 2A (Q35200574)

7 August 2017

title

Linkage analysis of a DNA marker localized to 20p12 and multiple endocrine neoplasia type 2A (English)

1 reference

multiple endocrine neoplasia type 2A

7 August 2017

main subject

1 reference

P J Goodfellow

1

1 reference

7 August 2017

B N White

2

1 reference

7 August 2017

J J Holden

3

1 reference

7 August 2017

A M Duncan

4

1 reference

7 August 2017

E V Sears

5

1 reference

7 August 2017

H S Wang

6

1 reference

7 August 2017

L Berlin

7

1 reference

7 August 2017

K K Kidd

8

1 reference

7 August 2017

N E Simpson

9

1 reference

7 August 2017

language of work or name

English

0 references

publication date

1 September 1985

1 reference

American Journal of Human Genetics

7 August 2017

published in

1 reference

7 August 2017

volume

37

1 reference

7 August 2017

issue

5

1 reference

7 August 2017

page(s)

890-897

1 reference

Multiple endocrine neoplasia, type II: a combined surgical and genetic approach to treatment

7 August 2017

cites work

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1684696

Expression of recessive alleles by chromosomal mechanisms in retinoblastoma

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1684696

Chromosome 20 deletion in human multiple endocrine neoplasia types 2A and 2B: a double-blind study

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1684696

Linkage data excluding a locus for multiple endocrine neoplasia type 2 syndromes from the distal part of the short arm of chromosome 11.

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1684696

Multiple endocrine neoplasia type 2 (Sipple's syndrome): clinical and cytogenetic analysis of a kindred

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1684696

Nonuniform recombination within the human beta-globin gene cluster

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1684696

Identification of a recent recombination event within the human beta-globin gene cluster

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1684696

Estimation of the recombination fraction in human pedigrees: efficient computation of the likelihood for human linkage studies

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1684696

Genetic mapping of DNA segments relative to the locus for the fragile-X syndrome at Xq27.3.

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1684696

Detection of specific sequences among DNA fragments separated by gel electrophoresis

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1684696

Labeling deoxyribonucleic acid to high specific activity in vitro by nick translation with DNA polymerase I

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1684696

Retinoblastoma and Subband Deletion of Chromosome 13

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1684696

Aniridia-Wilms’ tumor association: evidence for specific deletion of 11p13

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1684696

Chromosomal imbalance in the Aniridia-Wilms' tumor association: 11p interstitial deletion

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1684696

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1684696

Somatic deletion and duplication of genes on chromosome 11 in Wilms' tumours.

26 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1684696

Chromosomal deletion and retinoblastoma

26 September 2018

1 reference

12 December 2020

Measurement of urinary epinephrine in screening for pheochromocytoma in multiple endocrine neoplasia type II

1 reference

12 December 2020

Familial occurrence of the aniridia-Wilms tumor syndrome with deletion 11p13-14.1

1 reference

12 December 2020

Localization of single copy DNA sequences of G-banded human chromosomes by in situ hybridization

1 reference

12 December 2020

Chromosome Instability in Patients With Medullary Carcinoma of the Thyroid

1 reference

12 December 2020

Exclusion of linkage between the loci for multiple endocrine neoplasia type-2 (MEN-2) and HLA

1 reference

12 December 2020

Abnormalities of chromosome #13 in retinoblastomas from individuals with normal constitutional karyotypes

1 reference

12 December 2020

Chromosomal breakage in multiple endocrine adenomatosis (types I and II)

1 reference

12 December 2020

Linkage and chromosome study of multiple endocrine neoplasia IIa

1 reference

12 December 2020

Loss of alleles at loci on human chromosome 11 during genesis of Wilms' tumour

1 reference

12 December 2020

Development of homozygosity for chromosome 11p markers in Wilms' tumour

1 reference

12 December 2020

Loss of a Harvey ras allele in sporadic Wilms' tumour

1 reference

12 December 2020

Identifiers

PMC publication ID

1684696

1 reference

7 August 2017

1 reference