Molecular diagnosis of Huntington disease in Portugal: implications for genetic counselling and clinical practice.
about
Exclusion of mutations in the PRNP, JPH3, TBP, ATN1, CREBBP, POU3F2 and FTL genes as a cause of disease in Portuguese patients with a Huntington-like phenotype.The Prevalence of Juvenile Huntington's Disease: A Review of the Literature and Meta-Analysis.Genetic counseling and testing for Huntington's disease: A historical review.Genetic Counseling in Portugal: Education, Practice and a Developing Profession.Recommendations for the predictive genetic test in Huntington's disease.Huntington's disease in Greece: the experience of 14 years.High frequency of intermediate alleles on Huntington disease-associated haplotypes in British Columbia's general population.Huntington disease and Huntington disease-like in a case series from Brazil.Ancient origin of the CAG expansion causing Huntington disease in a Spanish population.
P2860
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P2860
Molecular diagnosis of Huntington disease in Portugal: implications for genetic counselling and clinical practice.
description
2003 nî lūn-bûn
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2003年の論文
@ja
2003年学术文章
@wuu
2003年学术文章
@zh
2003年学术文章
@zh-cn
2003年学术文章
@zh-hans
2003年学术文章
@zh-my
2003年学术文章
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2003年學術文章
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2003年學術文章
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name
Molecular diagnosis of Hunting ...... selling and clinical practice.
@en
Molecular diagnosis of Hunting ...... selling and clinical practice.
@nl
type
label
Molecular diagnosis of Hunting ...... selling and clinical practice.
@en
Molecular diagnosis of Hunting ...... selling and clinical practice.
@nl
prefLabel
Molecular diagnosis of Hunting ...... selling and clinical practice.
@en
Molecular diagnosis of Hunting ...... selling and clinical practice.
@nl
P2093
P2860
P50
P356
P1476
Molecular diagnosis of Hunting ...... selling and clinical practice.
@en
P2093
Cristina Januário
Isabel Gaspar
Laura Guimarães
Leal Loureiro
Marina Magalhães
Paula Magalhães
P2860
P2888
P304
P356
10.1038/SJ.EJHG.5201055
P50
P577
2003-11-01T00:00:00Z
P5875
P6179
1016623574