This site needs JavaScript to work properly. Please enable it to take advantage of the complete set of features!

Skip to main page content

Add to Collections

Your saved search

Name of saved search:

Search terms:

Test search terms

Would you like email updates of new search results?

Yes
No

Email: (change)

Frequency:

Which day?

Which day?

Report format:

Send at most:

Send even when there aren't any new results

Optional text in email:

Your RSS Feed

Comment

. 2010 Jul;12(7):411-2.

doi: 10.1097/GIM.0b013e3181e5c804.

Commentary on population screening for fragile X syndrome

Bradford Coffee¹

Affiliations

PMID: 20535018
DOI: 10.1097/GIM.0b013e3181e5c804

Free article

Comment

Commentary on population screening for fragile X syndrome

Bradford Coffee. Genet Med. 2010 Jul.

Free article

. 2010 Jul;12(7):411-2.

doi: 10.1097/GIM.0b013e3181e5c804.

Author

Bradford Coffee¹

Affiliation

¹ Department of Human Genetics, Emory University School of Medicine, Atlanta, GA 30322, USA. bcoffee@emory.edu

PMID: 20535018
DOI: 10.1097/GIM.0b013e3181e5c804

Erratum in

Genet Med. 2010 Aug;12(8):535

No abstract available

PubMed Disclaimer

Comment in

Methylation analysis of fragile X-related epigenetic elements may provide a suitable newborn screening test for fragile X syndrome.
Godler DE, Slater HR, Amor D, Loesch DZ. Godler DE, et al. Genet Med. 2010 Sep;12(9):595. doi: 10.1097/GIM.0b013e3181f07088. Genet Med. 2010. PMID: 20838083 Free PMC article. No abstract available.

Comment on

A systematic review of population screening for fragile X syndrome.
Hill MK, Archibald AD, Cohen J, Metcalfe SA. Hill MK, et al. Genet Med. 2010 Jul;12(7):396-410. doi: 10.1097/GIM.0b013e3181e38fb6. Genet Med. 2010. PMID: 20548240

Publication types

Actions

MeSH terms

Actions
Actions
Actions
Actions
Actions
Actions
Actions
Actions
Actions

LinkOut - more resources

Full Text Sources
- Elsevier Science
- Ovid Technologies, Inc.
Medical
- MedlinePlus Health Information