Pitfalls of automated comparative sequence analysis as a single platform for routine clinical testing for NF1.

Journal of medical genetics ·Vol. 42 ·No. 5 ·2005-05-00 ·页码 e25

Messiaen LM, Wimmer K

Abstract

暂无摘要

MeSH 主题词

DNA Mutational Analysis/methods Genes, Neurofibromatosis 1 Genetic Testing/methods Humans Mutation Neurofibromatosis 1/diagnosis Polymorphism, Genetic Sensitivity and Specificity

作者与单位

共 2 位作者，点击展开单位 / ORCID

Messiaen L M

Wimmer K

Article Info

Journal

Journal of medical genetics

Abbr.

J Med Genet

ISSN

1468-6244

Published

2005-05-00

页码

e25

Language

English

Country/Region

England

NLM ID

2985087R

勘误 / 撤稿关联

CommentOn

PMID: 15060124

CommentIn

PMID: 15937073

External Links

PubMed source View journal details

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Pitfalls of automated comparative sequence analysis as a single platform for routine clinical testing for NF1.

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