(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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scholarly article

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Europe PubMed Central

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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object named as

J. R. Howe

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25 October 2022

author name string

Wells SA Jr

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Europe PubMed Central

27 November 2017

Donis-Keller H

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Europe PubMed Central

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T. C. Lairmore

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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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W. G. Dilley

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L. Aine

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25 October 2022

E. Aine

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Europe PubMed Central

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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Europe PubMed Central

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

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

25 October 2022

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publication date

1 January 1991

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27 November 2017

full 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

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25 October 2022

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

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10.1016/0888-7543(91)90237-9

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25 October 2022

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Europe PubMed Central

27 November 2017

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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

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

25 October 2022

Familial Medullary Carcinoma Of The Thyroid

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10.1016/0888-7543(91)90237-9

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25 October 2022

A genetic linkage map of 32 loci on human chromosome 10

3

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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

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

5

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10.1016/0888-7543(91)90237-9

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25 October 2022

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

6

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10.1016/0888-7543(91)90237-9

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25 October 2022

A genetic linkage map of the human genome.

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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

12

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25 October 2022

Age-related probability of development of hereditary medullary thyroid carcinoma

13

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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

15

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

10.1016/0888-7543(91)90237-9

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25 October 2022

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

17

1 reference

10.1016/0888-7543(91)90237-9

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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

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25 October 2022

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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25 October 2022

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

25

1 reference

10.1016/0888-7543(91)90237-9

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

25 October 2022

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

26

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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

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

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1 reference

10.1016/0888-7543(91)90237-9

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

25 October 2022

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

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10.1016/0888-7543(91)90237-9

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25 October 2022

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

29

1 reference

10.1016/0888-7543(91)90237-9

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25 October 2022

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

30

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10.1016/0888-7543(91)90237-9

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25 October 2022

Deletion of genes on chromosome 1 in endocrine neoplasia

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10.1016/0888-7543(91)90237-9

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25 October 2022

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

32

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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

10.1016/0888-7543(91)90237-9

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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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25 October 2022

Linkage analysis of hereditary thyroid carcinoma with and without pheochromocytoma.

37

1 reference

10.1016/0888-7543(91)90237-9

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25 October 2022

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

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10.1016/0888-7543(91)90237-9

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

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25 October 2022

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

44

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10.1016/0888-7543(91)90237-9

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25 October 2022

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

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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

27 November 2017

1 reference

Europe PubMed Central

27 November 2017

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