MRI screening of kindred at risk of developing paragangliomas: support for genomic imprinting in hereditary glomus tumours.
about
The Dutch founder mutation SDHD.D92Y shows a reduced penetrance for the development of paragangliomas in a large multigenerational familyFirst experiences with genetic counselling based on predictive DNA diagnosis in hereditary glomus tumours (paragangliomas)Founder effect at PGL1 in hereditary head and neck paraganglioma families from the Netherlands.Laryngeal paraganglioma: a rare clinical entity managed by supraselective embolization and lateral pharygotomy.Novel mutations and the emergence of a common mutation in the SDHD gene causing familial paraganglioma.Sympathetic paraganglioma as an unusual cause of Horner's syndrome.
P2860
MRI screening of kindred at risk of developing paragangliomas: support for genomic imprinting in hereditary glomus tumours.
description
1992 nî lūn-bûn
@nan
1992年の論文
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1992年論文
@yue
1992年論文
@zh-hant
1992年論文
@zh-hk
1992年論文
@zh-mo
1992年論文
@zh-tw
1992年论文
@wuu
1992年论文
@zh
1992年论文
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name
MRI screening of kindred at ri ...... in hereditary glomus tumours.
@ast
MRI screening of kindred at ri ...... in hereditary glomus tumours.
@en
type
label
MRI screening of kindred at ri ...... in hereditary glomus tumours.
@ast
MRI screening of kindred at ri ...... in hereditary glomus tumours.
@en
prefLabel
MRI screening of kindred at ri ...... in hereditary glomus tumours.
@ast
MRI screening of kindred at ri ...... in hereditary glomus tumours.
@en
P2093
P2860
P356
P1476
MRI screening of kindred at ri ...... in hereditary glomus tumours.
@en
P2093
Maaswinkel-Mooy PD
Pauwels EK
Sandkuijl LA
van Gils AP
van der Mey AG
P2860
P2888
P304
P356
10.1038/BJC.1992.189
P407
P577
1992-06-01T00:00:00Z