Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
2
pubmed:dateCreated
2004-2-17
pubmed:language
ger
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
Feb
pubmed:issn
0017-6192
pubmed:author
pubmed:issnType
Print
pubmed:volume
52
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
150-2
pubmed:dateRevised
2005-11-17
pubmed:meshHeading
pubmed-meshheading:14968319-Abnormalities, Multiple, pubmed-meshheading:14968319-Child, Preschool, pubmed-meshheading:14968319-Chromosome Aberrations, pubmed-meshheading:14968319-Chromosomes, Human, Pair 17, pubmed-meshheading:14968319-Chromosomes, Human, Pair 7, pubmed-meshheading:14968319-Craniofacial Abnormalities, pubmed-meshheading:14968319-Developmental Disabilities, pubmed-meshheading:14968319-Diagnosis, Differential, pubmed-meshheading:14968319-Female, pubmed-meshheading:14968319-Fetal Growth Retardation, pubmed-meshheading:14968319-GRB10 Adaptor Protein, pubmed-meshheading:14968319-Genes, Dominant, pubmed-meshheading:14968319-Genes, Recessive, pubmed-meshheading:14968319-Humans, pubmed-meshheading:14968319-Infant, Newborn, pubmed-meshheading:14968319-Language Development Disorders, pubmed-meshheading:14968319-Male, pubmed-meshheading:14968319-Phenotype, pubmed-meshheading:14968319-Pregnancy, pubmed-meshheading:14968319-Proteins, pubmed-meshheading:14968319-Syndrome, pubmed-meshheading:14968319-Translocation, Genetic, pubmed-meshheading:14968319-Uniparental Disomy
pubmed:year
2004
pubmed:articleTitle
[Child language development delay in craniofacial dysplasia].
pubmed:affiliation
Klinik für Phoniatrie und Pädaudiologie, Medizinische Hochschule Hannover.
pubmed:publicationType
Journal Article, Case Reports