(Q43208691)

16 November 2017

Detecting polymorphisms and mutations in candidate genes (English)

1 reference

16 November 2017

Julianne S Collins

1

1 reference

16 November 2017

Charles E Schwartz

series ordinal

2

1 reference

16 November 2017

language of work or name

English

0 references

publication date

1 November 2002

1 reference

American Journal of Human Genetics

16 November 2017

1 reference

16 November 2017

71

1 reference

16 November 2017

5

1 reference

16 November 2017

1251-1252

1 reference

The HOXA1 A218G polymorphism and autism: lack of association in white and black patients from the South Carolina Autism Project

16 November 2017

1 reference

PubMed Central

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=385117

Monogenic causes of X-linked mental retardation.

25 May 2018

1 reference

PubMed Central

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=385117

PMP22 Thr(118)Met: recessive CMT1 mutation or polymorphism?

25 May 2018

1 reference

PubMed Central

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=385117

P1148A in fibrillin-1 is not a mutation anymore

25 May 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/12452182

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1086/344344

1 reference

16 November 2017

1 reference

16 November 2017

PubMed publication ID

12452182

1 reference