(Q43809602)

English

Familial medullary thyroid carcinoma and multiple endocrine neoplasia type 2B map to the same region of chromosome 10 as multiple endocrine neoplasia type 2A

scientific article published on January 1, 1991

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Europe PubMed Central

PubMed publication ID

27 November 2017

Familial medullary thyroid carcinoma and multiple endocrine neoplasia type 2B map to the same region of chromosome 10 as multiple endocrine neoplasia type 2A (English)

1 reference

10.1016/0888-7543(91)90237-9

https://api.crossref.org/works/10.1016/0888-7543(91)90237-9

25 October 2022

thyroid carcinoma

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based on heuristic

inferred from title

multiple endocrine neoplasia type 2B

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based on heuristic

inferred from title

familial medullary thyroid carcinoma

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based on heuristic

inferred from title

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10.1016/0888-7543(91)90237-9

https://api.crossref.org/works/10.1016/0888-7543(91)90237-9

25 October 2022

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J. R. Howe

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25 October 2022

author name string

Wells SA Jr

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PubMed publication ID

27 November 2017

Donis-Keller H

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PubMed publication ID

27 November 2017

T. C. Lairmore

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Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A1672289

25 October 2022

J. A. Korte

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25 October 2022

W. G. Dilley

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A1672289

25 October 2022

L. Aine

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Europe PubMed Central

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25 October 2022

E. Aine

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Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A1672289

25 October 2022

S. A. Wells

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1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A1672289

25 October 2022

H. Donis-Keller

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Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A1672289

25 October 2022

publication date

1 January 1991

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27 November 2017

language of work or name

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work available at URL

https://api.elsevier.com/content/article/PII:0888754391902379?httpAccept=text/xml

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10.1016/0888-7543(91)90237-9

https://api.crossref.org/works/10.1016/0888-7543(91)90237-9

25 October 2022

https://api.elsevier.com/content/article/PII:0888754391902379?httpAccept=text/plain

1 reference

10.1016/0888-7543(91)90237-9

https://api.crossref.org/works/10.1016/0888-7543(91)90237-9

25 October 2022

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Europe PubMed Central

PubMed publication ID

27 November 2017

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27 November 2017

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27 November 2017

181-192

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27 November 2017

Visible corneal nerve fibers and neuromas of the conjunctiva--a syndrome of type-3 multiple endocrine adenomatosis in two generations

1

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10.1016/0888-7543(91)90237-9

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25 October 2022

Familial Medullary Carcinoma Of The Thyroid

2

1 reference

10.1016/0888-7543(91)90237-9

https://api.crossref.org/works/10.1016/0888-7543(91)90237-9

25 October 2022

A genetic linkage map of 32 loci on human chromosome 10

3

1 reference

10.1016/0888-7543(91)90237-9

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25 October 2022

Exclusion of linkage of loci on chromosome 19 with multiple endocrine neoplasia, type 2

5

1 reference

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Chromosome-specific alpha satellite DNA: isolation and mapping of a polymorphic alphoid repeat from human chromosome 10

6

1 reference

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A genetic linkage map of the human genome

7

1 reference

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Very mild muscular dystrophy associated with the deletion of 46% of dystrophin

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

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A human DNA segment with properties of the gene that predisposes to retinoblastoma and osteosarcoma

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Age-related probability of development of hereditary medullary thyroid carcinoma

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Elevated levels of the alpha 5 beta 1 fibronectin receptor suppress the transformed phenotype of Chinese hamster ovary cells

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Genetic homogeneity between acute and chronic forms of spinal muscular atrophy

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1 reference

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25 October 2022

Assignment of the gene encoding the beta-subunit of the human fibronectin receptor (beta-FNR) to chromosome 10p11.2

16

1 reference

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25 October 2022

Medullary (solid) carcinoma of the thyroid; a clinicopathologic entity

17

1 reference

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25 October 2022

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

18

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Identification of the cystic fibrosis gene: genetic analysis

22

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Mutation and childhood cancer: a probabilistic model for the incidence of retinoblastoma

23

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Complete cloning of the duchenne muscular dystrophy (DMD) cDNA and preliminary genomic organization of the DMD gene in normal and affected individuals

24

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Loss of heterozygosity in three embryonal tumours suggests a common pathogenetic mechanism

25

1 reference

10.1016/0888-7543(91)90237-9

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25 October 2022

Development of multiple endocrine neoplasia type 2A does not involve substantial deletions of chromosome 10

26

1 reference

10.1016/0888-7543(91)90237-9

https://api.crossref.org/works/10.1016/0888-7543(91)90237-9

25 October 2022

Multiple endocrine neoplasia type 1 gene maps to chromosome 11 and is lost in insulinoma

27

1 reference

10.1016/0888-7543(91)90237-9

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Multilocus linkage analysis in humans: detection of linkage and estimation of recombination

28

1 reference

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Bgl II RFLP recognized by a human IRBP cDNA localized to chromosome 10.

29

1 reference

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A linked genetic marker for multiple endocrine neoplasia type 2A on chromosome 10

30

1 reference

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Deletion of genes on chromosome 1 in endocrine neoplasia

31

1 reference

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A polymorphic locus, D10S5, at 10q21.1.

32

1 reference

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A simple salting out procedure for extracting DNA from human nucleated cells

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An extended genetic linkage map of markers for human chromosome 10.

35

1 reference

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25 October 2022

Linked markers flanking the gene for multiple endocrine neoplasia type 2A.

36

1 reference

10.1016/0888-7543(91)90237-9

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Linkage analysis of hereditary thyroid carcinoma with and without pheochromocytoma

37

1 reference

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Low incidence of loss of chromosome 10 in sporadic and hereditary human medullary thyroid carcinoma

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Complete physical map of the WAGR region of 11p13 localizes a candidate Wilms' tumor gene

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Assignment of multiple endocrine neoplasia type 2A to chromosome 10 by linkage

44

1 reference

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Report of the committee on the genetic constitution of chromosomes 9 and 10.

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Genetic alterations during colorectal-tumor development

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Close linkage of MEN2A with RBP3 locus in Japanese kindreds

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25 October 2022

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10.1016/0888-7543(91)90237-9

1 reference

Europe PubMed Central

PubMed publication ID

27 November 2017

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

27 November 2017

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