(Q50502081)

14 March 2018

title

Familial carotid body paragangliomas and sensorineural hearing-loss: a new syndrome. (English)

1 reference

14 March 2018

1 reference

Lord RS

1

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14 March 2018

Chambers AJ

series ordinal

2

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14 March 2018

publication date

1 January 1999

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14 March 2018

published in

Vascular

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14 March 2018

volume

7

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14 March 2018

issue

1

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14 March 2018

page(s)

134-138

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14 March 2018

Genetic aspects of nonchromaffin paraganglioma

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Fine mapping of a putatively imprinted gene for familial non-chromaffin paragangliomas to chromosome 11q13.1: evidence for genetic heterogeneity

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MRI screening of kindred at risk of developing paragangliomas: support for genomic imprinting in hereditary glomus tumours

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A different kind of inheritance

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Association of thyroid carcinoma and chemodectoma

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7 January 2021

Carotid body tumours and other cervical paragangliomas: diagnosis and management in 25 patients

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7 January 2021

A gene subject to genomic imprinting and responsible for hereditary paragangliomas maps to chromosome 11q23-qter

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Linkage of autosomal dominant hearing loss to the short arm of chromosome 1 in two families

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The gene for an inherited form of deafness maps to chromosome 5q31

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Defective myosin VIIA gene responsible for Usher syndrome type 1B

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Identifiers

DOI

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14 March 2018

1 reference

14 March 2018