Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
8
pubmed:dateCreated
2002-8-5
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
Aug
pubmed:issn
1468-6244
pubmed:author
pubmed:issnType
Electronic
pubmed:volume
39
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
586-8
pubmed:dateRevised
2011-11-17
pubmed:meshHeading
pubmed-meshheading:12161600-Amino Acid Substitution, pubmed-meshheading:12161600-Brain Diseases, Metabolic, Inborn, pubmed-meshheading:12161600-Chromosomal Proteins, Non-Histone, pubmed-meshheading:12161600-CpG Islands, pubmed-meshheading:12161600-DNA-Binding Proteins, pubmed-meshheading:12161600-Developmental Disabilities, pubmed-meshheading:12161600-Female, pubmed-meshheading:12161600-Genetic Testing, pubmed-meshheading:12161600-Genetic Variation, pubmed-meshheading:12161600-Humans, pubmed-meshheading:12161600-Infant, pubmed-meshheading:12161600-Intellectual Disability, pubmed-meshheading:12161600-Male, pubmed-meshheading:12161600-Methyl-CpG-Binding Protein 2, pubmed-meshheading:12161600-Microcephaly, pubmed-meshheading:12161600-Pedigree, pubmed-meshheading:12161600-Point Mutation, pubmed-meshheading:12161600-Repressor Proteins, pubmed-meshheading:12161600-Rett Syndrome
pubmed:year
2002
pubmed:articleTitle
MECP2 gene nucleotide changes and their pathogenicity in males: proceed with caution.
pubmed:publicationType
Letter