Familial isolated hyperparathyroidism is linked to a 1.7 Mb region on chromosome 2p13.3-14 (Q24655804)

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D R Nyholt

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F Busfield

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M Epstein

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J Burgess

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S Stranks

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P Hill

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D Perry-Keene

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D Learoyd

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B Robinson

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J B Prins

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J W Cardinal

Journal of Medical Genetics

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language of work or name

English

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publication date

March 2006

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published in

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volume

43

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page(s)

e12

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issue

3

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cites work

Germline and de novo mutations in the HRPT2 tumour suppressor gene in familial isolated hyperparathyroidism (FIHP)

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Genetic testing in familial isolated hyperparathyroidism: unexpected results and their implications

7 April 2017

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

7 April 2017

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The protein phosphatase calcineurin determines basal parathyroid hormone gene expression

7 April 2017

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Identification and molecular characterization of two closely related G protein-coupled receptors activated by prokineticins/endocrine gland vascular endothelial growth factor

7 April 2017

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Parametric and nonparametric linkage analysis: a unified multipoint approach

7 April 2017

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Genetic dissection of complex traits: guidelines for interpreting and reporting linkage results

7 April 2017

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Faster sequential genetic linkage computations

7 April 2017

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Gland size is associated with changes in gene expression profiles in sporadic parathyroid adenomas

7 April 2017

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A combined linkage-physical map of the human genome

28 September 2017

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Molecular classification of parathyroid neoplasia by gene expression profiling

28 September 2017

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Involvement of protein kinase C-alpha and -epsilon in extracellular Ca(2+) signalling mediated by the calcium sensing receptor

28 September 2017

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Familial isolated hyperparathyroidism is rarely caused by germline mutation in HRPT2, the gene for the hyperparathyroidism-jaw tumor syndrome.

28 September 2017

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HRPT2, encoding parafibromin, is mutated in hyperparathyroidism-jaw tumor syndrome

28 September 2017

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Familial isolated hyperparathyroidism: clinical and genetic characteristics of 36 kindreds

28 September 2017

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Statistical tests for detection of misspecified relationships by use of genome-screen data

28 September 2017

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Highly polymorphic sequence variation in calcineurin B coding region (PPP3R1).

28 September 2017

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Computer-simulation methods in human linkage analysis

28 September 2017

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A rapid non-enzymatic method for the preparation of HMW DNA from blood for RFLP studies

28 September 2017

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Summary statement from a workshop on asymptomatic primary hyperparathyroidism: a perspective for the 21st century

28 September 2017

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inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Expression of the MEN-1 gene in a large kindred with multiple endocrine neoplasia type 1

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https://pubmed.ncbi.nlm.nih.gov/16525030