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PMID: 12452182 Published · ppublish English Letter Research Support, U.S. Gov't, P.H.S.

Detecting polymorphisms and mutations in candidate genes.

American journal of human genetics ·Vol. 71 ·No. 5 ·2002-11-00 ·Pages 1251-2

Collins JS, Schwartz CE

Abstract

暂无摘要

MeSH Terms

Case-Control Studies Chromosomes, Human, X DNA Mutational Analysis Female Gene Frequency Humans Male Mutation Polymorphism, Genetic

Authors & Affiliations

2 authors, click to expand affiliations / ORCID

Collins Julianne S

Schwartz Charles E

References (4)

4 references, click to expand

P1148A in fibrillin-1 is not a mutation anymore.
Nat Genet. 1997 Jan;15(1):12 PMID: 8988160
The HOXA1 A218G polymorphism and autism: lack of association in white and black patients from the South Carolina Autism Project.
J Autism Dev Disord. 2003 Jun;33(3):343-8 PMID: 12908836
PMP22 Thr(118)Met: recessive CMT1 mutation or polymorphism?
Nat Genet. 1997 Jan;15(1):13-4 PMID: 8988161
Monogenic causes of X-linked mental retardation.
Nat Rev Genet. 2001 Sep;2(9):669-80 PMID: 11533716

Article Info

Journal

American journal of human genetics

Abbr.

Am J Hum Genet

ISSN

0002-9297

DOI

Published

2002-11-00

Pages

1251-2

Language

English

Region

United States

NLM ID

0370475

PMCID

PMC385117

Subset

Grants

NICHD NIH HHS · R01 HD026202 · United States

NIMH NIH HHS · R24 MH057840 · United States

NICHD NIH HHS · HD26202 · United States

NIMH NIH HHS · MH57840 · United States

External Links

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