Re: Pitfalls of automated comparative sequence analysis as a single platform for routine clinical testing for NF1 (Messiaen and Wimmer).

Journal of medical genetics ·Vol. 42 ·No. 7 ·2005-07-00 ·页码 e41

Whittaker JL, Mattocks C, Baralle D, Tarpey P, ffrench-Constant C, Bobrow M

Abstract

暂无摘要

MeSH 主题词

Autoanalysis Diagnostic Tests, Routine Humans Mutation Neurofibromatosis 1/diagnosis,genetics Sequence Analysis, DNA/instrumentation,methods

作者与单位

共 6 位作者，点击展开单位 / ORCID

Whittaker J L

Mattocks C

Baralle D

Tarpey P

ffrench-Constant C

Bobrow M

Article Info

Journal

Journal of medical genetics

Abbr.

J Med Genet

ISSN

1468-6244

Published

2005-07-00

页码

e41

Language

English

Country/Region

England

NLM ID

2985087R

勘误 / 撤稿关联

CommentOn

PMID: 15060124

External Links

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