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Genetic disorders of thyroid metabolism and brain developmentFamilial essential ("benign") chorea.Benign familial chorea: an association with intellectual impairment.Hereditary progressive chorea without dementia.Benign hereditary chorea--entity or syndrome?A novel de novo mutation of the TITF1/NKX2-1 gene causing ataxia, benign hereditary chorea, hypothyroidism and a pituitary mass in a UK family and review of the literature.Benign hereditary chorea of early onset maps to chromosome 14q.Benign (non-paroxysmal) familial chorea. Paediatric perspectivesBenign hereditary chorea: clinical and neuroimaging features in an Italian family.[Juvenile hereditary chorea. Study of a family with recessive pattern of transmission]Benign hereditary chorea related to NKX2.1: expansion of the genotypic and phenotypic spectrum.
P2860
Q26858956-BB9E78F5-158D-4928-8D20-A1F859696116Q33587131-12BDC504-6000-4480-85B6-8DFDED921FECQ33619742-3B75EC5F-1843-4D32-8CD6-555C43E56F80Q33627386-2FA17F73-C0E6-4450-8813-FF48F770F7CEQ33884389-1BF3BBC8-5850-48B1-A458-1672D1789E78Q34136479-A04F1BAB-8B79-4C76-A0FF-07C3ED51696AQ34146067-2F036CBF-0615-4F3E-B986-53FB0B24D882Q35115187-6E256C2D-2C66-4D43-A3DF-7D90552CE143Q42472823-C05F1A62-B49B-4433-879D-0DDCA0168087Q45288956-A48E8EA4-0B37-4BFC-8C62-C6C705838A24Q48905953-BC84BB80-234D-44EE-AD77-3EBF1EE919AA
P2860
description
1973 nî lūn-bûn
@nan
1973年の論文
@ja
1973年学术文章
@wuu
1973年学术文章
@zh
1973年学术文章
@zh-cn
1973年学术文章
@zh-hans
1973年学术文章
@zh-my
1973年学术文章
@zh-sg
1973年學術文章
@yue
1973年學術文章
@zh-hant
name
Benign familial chorea with onset in childhood.
@en
Benign familial chorea with onset in childhood.
@nl
type
label
Benign familial chorea with onset in childhood.
@en
Benign familial chorea with onset in childhood.
@nl
prefLabel
Benign familial chorea with onset in childhood.
@en
Benign familial chorea with onset in childhood.
@nl
P2093
P1476
Benign familial chorea with onset in childhood.
@en
P2093
B J Mansheim
G J Wolcott
P304
P356
10.1001/JAMA.1973.03220410017004
P407
P577
1973-09-01T00:00:00Z