Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
11
pubmed:dateCreated
2008-11-3
pubmed:abstractText
Haploinsufficiency of the gene encoding for transcription factor 4 (TCF4) was recently identified as the underlying cause of Pitt-Hopkins syndrome (PTHS), an underdiagnosed mental-retardation syndrome characterised by a distinct facial gestalt, breathing anomalies and severe mental retardation.
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
Nov
pubmed:issn
1468-6244
pubmed:author
pubmed:issnType
Electronic
pubmed:volume
45
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
738-44
pubmed:dateRevised
2011-11-17
pubmed:meshHeading
pubmed-meshheading:18728071-Adolescent, pubmed-meshheading:18728071-Apnea, pubmed-meshheading:18728071-Basic Helix-Loop-Helix Leucine Zipper Transcription Factors, pubmed-meshheading:18728071-Child, pubmed-meshheading:18728071-Child, Preschool, pubmed-meshheading:18728071-DNA Mutational Analysis, pubmed-meshheading:18728071-DNA-Binding Proteins, pubmed-meshheading:18728071-Face, pubmed-meshheading:18728071-Female, pubmed-meshheading:18728071-Genotype, pubmed-meshheading:18728071-Humans, pubmed-meshheading:18728071-Hyperventilation, pubmed-meshheading:18728071-Infant, pubmed-meshheading:18728071-Intellectual Disability, pubmed-meshheading:18728071-Male, pubmed-meshheading:18728071-Microcephaly, pubmed-meshheading:18728071-Phenotype, pubmed-meshheading:18728071-Syndrome, pubmed-meshheading:18728071-Transcription Factors, pubmed-meshheading:18728071-Young Adult
pubmed:year
2008
pubmed:articleTitle
Further delineation of Pitt-Hopkins syndrome: phenotypic and genotypic description of 16 novel patients.
pubmed:publicationType
Letter, Research Support, Non-U.S. Gov't