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PMID |
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TITLE |
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Evaluation of Nyholt's procedure for multiple testing correction - author's reply. |
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ABSTRACT |
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DATE PUBLISHED |
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HISTORY |
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PUBSTATUS |
PUBSTATUSDATE |
received |
2005/07/03 |
accepted |
2005/07/05 |
aheadofprint |
2005/08/05 |
pubmed |
2005/09/03 09:00 |
medline |
2005/11/11 09:00 |
entrez |
2005/09/03 09:00 |
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AUTHORS |
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NAME |
COLLECTIVENAME |
LASTNAME |
FORENAME |
INITIALS |
AFFILIATION |
AFFILIATIONINFO |
Nyholt DR |
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Nyholt |
Dale R |
DR |
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Queensland Institute of Medical Research, Brisbane, Australia. |
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INVESTIGATORS |
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JOURNAL |
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VOLUME: 60 |
ISSUE: 1 |
TITLE: Human heredity |
ISOABBREVIATION: Hum. Hered. |
YEAR: 2005 |
MONTH: |
DAY: |
MEDLINEDATE: |
SEASON: |
CITEDMEDIUM: Print |
ISSN: 0001-5652 |
ISSNTYPE: Print |
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MEDLINE JOURNAL |
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MEDLINETA: Hum Hered |
COUNTRY: Switzerland |
ISSNLINKING: 0001-5652 |
NLMUNIQUEID: 0200525 |
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PUBLICATION TYPE |
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PUBLICATIONTYPE TEXT |
Comment |
Editorial |
Research Support, Non-U.S. Gov't |
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COMMENTS AND CORRECTIONS |
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REFTYPE |
REFSOURCE |
REFPMID |
NOTE |
CommentOn |
Hum Hered. 2005;60(1):19-25; discussion 61-2 |
16118503 |
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GRANTS |
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GENERAL NOTE |
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KEYWORDS |
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MESH HEADINGS |
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DESCRIPTORNAME |
QUALIFIERNAME |
Genetic Diseases, Inborn |
genetics |
Genotype |
genetics |
Haplotypes |
genetics |
Humans |
genetics |
Linkage Disequilibrium |
genetics |
Models, Genetic |
genetics |
Polymorphism, Single Nucleotide |
genetics |
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SUPPLEMENTARY MESH |
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GENE SYMBOLS |
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CHEMICALS |
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OTHER ID's |
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