|
rdf:type |
|
|
lifeskim:mentions |
|
|
pubmed:issue |
3
|
|
pubmed:dateCreated |
2006-3-6
|
|
pubmed:abstractText |
To describe the prenatal phenotype of the 11q deletion syndrome (Jacobsen syndrome) and present the molecular characterization of the deletion in the case presented.
|
|
pubmed:language |
eng
|
|
pubmed:journal |
|
|
pubmed:citationSubset |
IM
|
|
pubmed:status |
MEDLINE
|
|
pubmed:month |
Mar
|
|
pubmed:issn |
0197-3851
|
|
pubmed:author |
|
|
pubmed:copyrightInfo |
2006 John Wiley & Sons, Ltd.
|
|
pubmed:issnType |
Print
|
|
pubmed:volume |
26
|
|
pubmed:owner |
NLM
|
|
pubmed:authorsComplete |
Y
|
|
pubmed:pagination |
286-90
|
|
pubmed:meshHeading |
pubmed-meshheading:16506277-Abnormalities, Multiple,
pubmed-meshheading:16506277-Adult,
pubmed-meshheading:16506277-Chromosome Deletion,
pubmed-meshheading:16506277-Chromosomes, Human, Pair 11,
pubmed-meshheading:16506277-Craniofacial Abnormalities,
pubmed-meshheading:16506277-Female,
pubmed-meshheading:16506277-Fetal Diseases,
pubmed-meshheading:16506277-Humans,
pubmed-meshheading:16506277-Phenotype,
pubmed-meshheading:16506277-Pregnancy,
pubmed-meshheading:16506277-Ultrasonography, Prenatal
|
|
pubmed:year |
2006
|
|
pubmed:articleTitle |
Prenatal diagnosis of a large de novo terminal deletion of chromosome 11q.
|
|
pubmed:affiliation |
Institute of Human Genetics, University of Goettingen, Goettingen, Germany.
|
|
pubmed:publicationType |
Journal Article,
Case Reports
|
