(Q47793767)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9677065%20AND%20SRC:MED&resulttype=core&format=json

13 November 2019

title

Novel point mutation in exon 10 of the RET proto-oncogene in a family with medullary thyroid carcinoma (English)

1 reference

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13 November 2019

author

Ricardo V. García-Mayor

4

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13 November 2019

author name string

J Oriola

1

1 reference

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13 November 2019

C Páramo

2

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13 November 2019

I Halperin

3

1 reference

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13 November 2019

F Rivera-Fillat

5

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13 November 2019

publication date

1 July 1998

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American Journal of Medical Genetics Part A

13 November 2019

published in

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13 November 2019

volume

78

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13 November 2019

issue

3

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13 November 2019

page(s)

271-273

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Single missense mutation in the tyrosine kinase catalytic domain of the RET protooncogene is associated with multiple endocrine neoplasia type 2B

13 November 2019

cites work

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819980707%2978%3A3%3C271%3A%3AAID-AJMG13%3E3.0.CO%3B2-C

Mutations in the RET proto-oncogene are associated with MEN 2A and FMTC.

21 January 2018

1 reference

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Point mutation within the tyrosine kinase domain of the RET proto-oncogene in multiple endocrine neoplasia type 2B and related sporadic tumours

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819980707%2978%3A3%3C271%3A%3AAID-AJMG13%3E3.0.CO%3B2-C

The relationship between specific RET proto-oncogene mutations and disease phenotype in multiple endocrine neoplasia type 2. International RET mutation consortium analysis

21 January 2018

1 reference

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A Comparison of Pentagastrin Injection and Calcium Infusion as Provocative Agents for the Detection of Medullary Carcinoma of the Thyroid1

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819980707%2978%3A3%3C271%3A%3AAID-AJMG13%3E3.0.CO%3B2-C

RET receptor tyrosine kinase gene mutations: molecular biological, physiological and clinical aspects

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819980707%2978%3A3%3C271%3A%3AAID-AJMG13%3E3.0.CO%3B2-C

Germ-line mutations of the RET proto-oncogene in multiple endocrine neoplasia type 2A.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819980707%2978%3A3%3C271%3A%3AAID-AJMG13%3E3.0.CO%3B2-C

Germline mutation of RET codon 883 in two cases of de novo MEN 2B.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819980707%2978%3A3%3C271%3A%3AAID-AJMG13%3E3.0.CO%3B2-C

A mutation in the RET proto-oncogene associated with multiple endocrine neoplasia type 2B and sporadic medullary thyroid carcinoma

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819980707%2978%3A3%3C271%3A%3AAID-AJMG13%3E3.0.CO%3B2-C

Specific mutations of the RET proto-oncogene are related to disease phenotype in MEN 2A and FMTC

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819980707%2978%3A3%3C271%3A%3AAID-AJMG13%3E3.0.CO%3B2-C

Mutation of RET codon 768 is associated with the FMTC phenotype

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819980707%2978%3A3%3C271%3A%3AAID-AJMG13%3E3.0.CO%3B2-C

Germline dinucleotide mutation in codon 883 of the RET proto-oncogene in multiple endocrine neoplasia type 2B without codon 918 mutation

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819980707%2978%3A3%3C271%3A%3AAID-AJMG13%3E3.0.CO%3B2-C

Mutation analysis of the RET proto-oncogene in Dutch families with MEN 2A, MEN 2B and FMTC: two novel mutations and one de novo mutation for MEN 2A

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819980707%2978%3A3%3C271%3A%3AAID-AJMG13%3E3.0.CO%3B2-C

Clinical screening as compared with DNA analysis in families with multiple endocrine neoplasia type 2A

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819980707%2978%3A3%3C271%3A%3AAID-AJMG13%3E3.0.CO%3B2-C

Genotype‐phenotype correlation in multiple endocrine neoplasia type 2: report of the International RET Mutation Consortium

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819980707%2978%3A3%3C271%3A%3AAID-AJMG13%3E3.0.CO%3B2-C

RET proto-oncogene mutations in French MEN 2A and FMTC families

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819980707%2978%3A3%3C271%3A%3AAID-AJMG13%3E3.0.CO%3B2-C

10.1002/(SICI)1096-8628(19980707)78:3<271::AID-AJMG13>3.0.CO;2-C

21 January 2018

Identifiers

DOI

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9677065%20AND%20SRC:MED&resulttype=core&format=json

13 November 2019

1 reference