Linked Life Data

12174011

Source:http://linkedlifedata.com/resource/pubmed/id/12174011

Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
4
pubmed:dateCreated
2002-8-13
pubmed:abstractText
3-M syndrome is a rare, autosomal recessive dwarfing syndrome characterized by prenatal growth restriction, facial dysmorphism and absence of both microcephaly and mental retardation. The term 3-M syndrome originates from the common initial of the first three authors of the first report. The diagnosis is established by a combination of clinical history, clinical examination and radiographic findings. The present report shows two sisters whose facial features were slightly different from those usually reported. In addition, they presented with small nails and abnormal dermatoglyphics. The present report expands the phenotypic spectrum of 3-M syndrome.
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:status
MEDLINE
pubmed:month
Aug
pubmed:issn
1034-4810
pubmed:author
pubmed:issnType
Print
pubmed:volume
38
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
419-22
pubmed:dateRevised
2007-9-24
pubmed:meshHeading
pubmed:year
2002
pubmed:articleTitle
3-M syndrome in two sisters.
pubmed:affiliation
Ambulant Centre for Defects of Locomotor, Department of Anthropology and Human Genetics, The Faculty of Science, Charles University, Prague, Czech Republic.
pubmed:publicationType
Journal Article, Case Reports