Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
9
pubmed:dateCreated
2001-9-20
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
Sep
pubmed:issn
1468-6244
pubmed:author
pubmed:issnType
Electronic
pubmed:volume
38
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
624-9
pubmed:dateRevised
2009-11-19
pubmed:meshHeading
pubmed-meshheading:11565550-Alleles, pubmed-meshheading:11565550-Base Sequence, pubmed-meshheading:11565550-Blotting, Western, pubmed-meshheading:11565550-Child, Preschool, pubmed-meshheading:11565550-DNA Mutational Analysis, pubmed-meshheading:11565550-Female, pubmed-meshheading:11565550-Fragile X Mental Retardation Protein, pubmed-meshheading:11565550-Fragile X Syndrome, pubmed-meshheading:11565550-Gene Deletion, pubmed-meshheading:11565550-Genetic Testing, pubmed-meshheading:11565550-Humans, pubmed-meshheading:11565550-Infant, pubmed-meshheading:11565550-Infant, Newborn, pubmed-meshheading:11565550-Male, pubmed-meshheading:11565550-Nerve Tissue Proteins, pubmed-meshheading:11565550-Nuclear Proteins, pubmed-meshheading:11565550-Pedigree, pubmed-meshheading:11565550-Polymerase Chain Reaction, pubmed-meshheading:11565550-RNA-Binding Proteins, pubmed-meshheading:11565550-Sequence Deletion, pubmed-meshheading:11565550-Trans-Activators, pubmed-meshheading:11565550-Trinucleotide Repeats
pubmed:year
2001
pubmed:articleTitle
Microdeletion in the FMR-1 gene: an apparent null allele using routine clinical PCR amplification.
pubmed:publicationType
Letter, Case Reports, Research Support, Non-U.S. Gov't