(Q36258020)

13 August 2017

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

1 reference

multiple endocrine neoplasia

13 August 2017

1 reference

V R Babu

1

1 reference

13 August 2017

D L Van Dyke

series ordinal

2

1 reference

13 August 2017

C E Jackson

series ordinal

3

1 reference

13 August 2017

language of work or name

English

0 references

publication date

1 April 1984

1 reference

13 August 2017

4

1 reference

Proceedings of the National Academy of Sciences of the United States of America

inferred from page(s)

published in

1 reference

13 August 2017

81

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13 August 2017

8

1 reference

13 August 2017

2525-2528

1 reference

High resolution chromosome banding in the Rubinstein-Taybi syndrome.

13 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=345095

Expression of recessive alleles by chromosomal mechanisms in retinoblastoma

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=345095

Normal chromosomes in mucosol neuroma variant of medullary thyroid carcinoma syndrome

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=345095

Mutation and cancer: statistical study of retinoblastoma

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=345095

Adrenal medullary hyperplasia. A morphometric analysis in patients with familial medullary thyroid carcinoma

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=345095

Retinoblastoma A Model of Hereditary Fragile Chromosomal Regions

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=345095

Adrenal medullary disease in multiple endocrine neoplasia, type 2: pheochromocytoma and its precursors

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=345095

The two-mutational-event theory in medullary thyroid cancer

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=345095

The characterization of high-resolution G-banded chromosomes of man

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=345095

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

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=345095

Familial Retinoblastoma and Chromosome 13 Deletion Transmitted via an Insertional Translocation

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=345095

Possible linear order of genes for endocrine neoplasia type 2, the P red cell antigen and HL-A on chromosome 6.

29 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=345095

Deletion of the short arms of chromosome 20

29 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=345095

Quantitative analysis of high-resolution trypsin-giemsa bands on human prometaphase chromosomes

29 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=345095

Retinoblastoma and Subband Deletion of Chromosome 13

29 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=345095

Inherited Medullary Thyroid Carcinoma: A Final Monoclonal Mutation in One of Multiple Clones of Susceptible Cells

29 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=345095

G-banding patterns of high-resolution human chromosomes 6?22, X, and Y

29 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=345095

Hereditary Renal-Cell Carcinoma Associated with a Chromosomal Translocation

29 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=345095

Patient with 13 Chromosome Deletion: Evidence That the Retinoblastoma Gene Is a Recessive Cancer Gene

29 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=345095

C-Cell Hyperplasia Preceding Medullary Thyroid Carcinoma

22 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=345095

Chromosomal analysis of a human retinoblastoma

22 September 2018

1 reference

12 December 2020

Detection of medullary thyroid cancer by calcitonin assay in families

1 reference

12 December 2020

Chromosomal deletion and retinoblastoma

1 reference

12 December 2020

Clinical characteristics distinguishing hereditary from sporadic medullary thyroid carcinoma. Treatment implications

1 reference

12 December 2020

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

1 reference

12 December 2020

A deleted chromosome no. 13 in human retinoblastoma cells: relevance to tumorigenesis

1 reference

12 December 2020

Lymphocyte chromosome survey in 42 patients with retinoblastoma: Effort to detect 13q14 deletion mosaicism

1 reference

12 December 2020

Chromosome Instability in Patients With Medullary Carcinoma of the Thyroid

1 reference

12 December 2020

The human genes for S-adenosylhomocysteine hydrolase and adenosine deaminase are syntenic on chromosome 20

1 reference

12 December 2020

Familial renal cell carcinoma with a 3;11 chromosome translocation limited to tumor cells

1 reference

12 December 2020

Translocation(X;Y)(p22.33;p11.2) in XX males: etiology of male phenotype

1 reference

12 December 2020

Linkage and chromosome study of multiple endocrine neoplasia IIa

1 reference

12 December 2020

Phenotype mapping of the multiple endocrine neoplasia type II syndrome

1 reference

12 December 2020

Chromosomes in Sipple's syndrome

1 reference

12 December 2020

Identifiers

DOI

10.1073/PNAS.81.8.2525

1 reference

13 August 2017

0 references

1 reference

13 August 2017

PubMed publication ID

6585814

1 reference