| Commentary on population screening for fragile X syndrome. | |
| | |
MedLine Citation:
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PMID: 20535018 Owner: NLM Status: MEDLINE |
Abstract/OtherAbstract:
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Authors:
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Bradford Coffee |
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Publication Detail:
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Type: Comment; Journal Article |
Journal Detail:
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Title: Genetics in medicine : official journal of the American College of Medical Genetics Volume: 12 ISSN: 1530-0366 ISO Abbreviation: Genet. Med. Publication Date: 2010 Jul |
Date Detail:
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Created Date: 2010-07-15 Completed Date: 2010-10-21 Revised Date: - |
Medline Journal Info:
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Nlm Unique ID: 9815831 Medline TA: Genet Med Country: United States |
Other Details:
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Languages: eng Pagination: 411-2 Citation Subset: IM |
Affiliation:
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Department of Human Genetics, Emory University School of Medicine, Atlanta, GA 30322, USA. bcoffee@emory.edu |
Export Citation:
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APA/MLA Format Download EndNote Download BibTex |
| MeSH Terms | |
Descriptor/Qualifier:
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Female Fragile X Syndrome / diagnosis*, genetics Genetic Testing* Humans Infant, Newborn Neonatal Screening* Pregnancy Prenatal Diagnosis |
| Comments/Corrections | |
Comment On:
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Genet Med. 2010 Jul;12(7):396-410
[PMID:
20548240
]
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Comment In:
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Genet Med. 2010 Sep;12(9):595
[PMID:
20838083
]
|
Erratum In:
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Genet Med. 2010 Aug;12(8):535 |
From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine
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