(Q43641010)

25 November 2017

Familial isolated parathyroid adenoma in a consanguineous family (English)

1 reference

25 November 2017

1 reference

C Bergwitz

1

1 reference

25 November 2017

B Bremer

2

1 reference

25 November 2017

B Soudah

3

1 reference

25 November 2017

B Mayr

4

1 reference

25 November 2017

G Brabant

5

1 reference

25 November 2017

1 May 2001

1 reference

Journal of Endocrinological Investigation

25 November 2017

1 reference

25 November 2017

24

1 reference

25 November 2017

5

1 reference

25 November 2017

349-355

1 reference

https://scigraph.springernature.com/pub.10.1007/bf03343872

25 November 2017

0 references

cites work

Germline and somatic mutation of the gene for multiple endocrine neoplasia type 1 (MEN1)

1 reference

https://api.crossref.org/works/10.1007%2FBF03343872

No evidence for mutations in the calcium-sensing receptor gene in sporadic parathyroid adenomas.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FBF03343872

Positional cloning of the gene for multiple endocrine neoplasia-type 1

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FBF03343872

Identification of the multiple endocrine neoplasia type 1 (MEN1) gene. The European Consortium on MEN1

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FBF03343872

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FBF03343872

Familial isolated primary hyperparathyroidism.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FBF03343872

Expression of Ret/PTC1, -2, -3, -delta3 and -4 in German papillary thyroid carcinoma.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FBF03343872

Mutations in the human Ca(2+)-sensing receptor gene cause familial hypocalciuric hypercalcemia and neonatal severe hyperparathyroidism

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FBF03343872

Familial isolated hyperparathyroidism maps to the hyperparathyroidism-jaw tumor locus in 1q21-q32 in a subset of families

21 January 2018

1 reference

12 December 2020

Familial isolated hyperparathyroidism: a distinct genetic entity with an increased risk of parathyroid cancer

1 reference

12 December 2020

Loss of the retinoblastoma tumor-suppressor gene in parathyroid carcinoma

1 reference

12 December 2020

A new syndrome of autosomal recessive nephropathy, deafness, and hyperparathyroidism

1 reference

12 December 2020

Genetic basis of endocrine disease 5. Molecular genetics of parathyroid gland neoplasia

1 reference

12 December 2020

Is familial hyperparathyroidism a unique disease?

1 reference

12 December 2020

Autosomal recessive inheritance of familial hyperparathyroidism

1 reference

12 December 2020

Hereditary hyperparathyroidism-jaw tumor syndrome: the endocrine tumor gene HRPT2 maps to chromosome 1q21-q31

1 reference

12 December 2020

Germline mutations of the MEN1 gene in familial multiple endocrine neoplasia type 1 and related states

1 reference

12 December 2020

Mapping the Gene Causing Hereditary Primary Hyperparathyroidism in a Portuguese Kindred to Chromosome 1q22-q31

1 reference

12 December 2020

Menin mutations in patients with multiple endocrine neoplasia type 1

1 reference

12 December 2020

Parathyroid MEN1 gene mutations in relation to clinical characteristics of nonfamilial primary hyperparathyroidism

1 reference

12 December 2020

Identifiers

DOI

10.1007/BF03343872

1 reference

Dimensions Publication ID

25 November 2017

0 references

1 reference