15834242

Source:http://linkedlifedata.com/resource/pubmed/id/15834242

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Predicate	Object
rdf:type	pubmed:Citation
lifeskim:mentions	umls-concept:C0016667, umls-concept:C0220908, umls-concept:C0542559, umls-concept:C0560175, umls-concept:C1257802, umls-concept:C1706209
pubmed:issue	4
pubmed:dateCreated	2005-4-18
pubmed:abstractText	To document our experience with fragile X carrier screening.
pubmed:language	eng
pubmed:journal	http://linkedlifedata.com/resource/pubmed/journal/9815831
pubmed:citationSubset	IM
pubmed:chemical	http://linkedlifedata.com/resource/pubmed/chemical/FMR1 protein, human, http://linkedlifedata.com/resource/pubmed/chemical/Fragile X Mental Retardation Protein, http://linkedlifedata.com/resource/pubmed/chemical/Nerve Tissue Proteins, http://linkedlifedata.com/resource/pubmed/chemical/RNA-Binding Proteins
pubmed:status	MEDLINE
pubmed:month	Apr
pubmed:issn	1098-3600
pubmed:author	pubmed-author:CronisterAmyA, pubmed-author:DiMaioMiriamM, pubmed-author:DonnenfeldAlan EAE, pubmed-author:HallamStephanieS, pubmed-author:MahoneyMaurice JMJ
pubmed:issnType	Print
pubmed:volume	7
pubmed:owner	NLM
pubmed:authorsComplete	Y
pubmed:pagination	246-50
pubmed:dateRevised	2009-11-19
pubmed:meshHeading	pubmed-meshheading:15834242-Age Factors, pubmed-meshheading:15834242-Blotting, Southern, pubmed-meshheading:15834242-Female, pubmed-meshheading:15834242-Fragile X Mental Retardation Protein, pubmed-meshheading:15834242-Fragile X Syndrome, pubmed-meshheading:15834242-Gene Frequency, pubmed-meshheading:15834242-Genetic Counseling, pubmed-meshheading:15834242-Genetic Testing, pubmed-meshheading:15834242-Humans, pubmed-meshheading:15834242-Logistic Models, pubmed-meshheading:15834242-Maternal Exposure, pubmed-meshheading:15834242-Mutation, pubmed-meshheading:15834242-Nerve Tissue Proteins, pubmed-meshheading:15834242-Patient Acceptance of Health Care, pubmed-meshheading:15834242-Polymerase Chain Reaction, pubmed-meshheading:15834242-RNA-Binding Proteins, pubmed-meshheading:15834242-Trinucleotide Repeat Expansion
pubmed:year	2005
pubmed:articleTitle	Fragile X syndrome carrier screening in the prenatal genetic counseling setting.
pubmed:affiliation	Genetic Services and Molecular Diagnostic Laboratory, Genzyme Genetics, Westborough, Massachusetts, USA.
pubmed:publicationType	Journal Article