SPARQL
Query
Update
Search
Quick
Advanced
Co-occurrence
RelFinder
About
Sources
Admin
System Info
Repository Management
Search Configuration
Sources
10680333
Source:
http://linkedlifedata.com/resource/pubmed/id/10680333
Search
Subject
(
62
)
Predicate
Object
All
Download in:
JSON
RDF
N3/Turtle
N-Triples
Switch to
Custom View
Named Graph
All
UniProt
NCBIGene
DrugBank
ClinicalTrials
UMLS
PubMed
Mappings
MentionedEntities
Language
All
English
Español
Português
Français
Deutsch
Русский
日本語
Български
Inference
Explicit and implicit
Explicit only
Implicit only
Statements in which the resource exists as a subject.
Predicate
Object
rdf:type
pubmed:Citation
lifeskim:mentions
umls-concept:C0008625
,
umls-concept:C0008626
,
umls-concept:C0013080
,
umls-concept:C0026591
,
umls-concept:C0034897
,
umls-concept:C0035647
,
umls-concept:C0152095
,
umls-concept:C0152096
,
umls-concept:C0521457
,
umls-concept:C0936012
,
umls-concept:C1556094
pubmed:issue
6
pubmed:dateCreated
2000-3-7
pubmed:abstractText
To evaluate the risk of recurrence of fetal chromosomal aberrations in women who had offspring with numeric chromosomal abnormalities.
pubmed:language
eng
pubmed:journal
http://linkedlifedata.com/resource/pubmed/journal/9612761
pubmed:citationSubset
IM
pubmed:status
MEDLINE
pubmed:month
Dec
pubmed:issn
1341-8076
pubmed:author
pubmed-author:FujimoriKK
,
pubmed-author:FujimotoSS
,
pubmed-author:HiraharaFF
,
pubmed-author:HoshiNN
,
pubmed-author:MaedaTT
,
pubmed-author:UeharaSS
,
pubmed-author:YaegashiNN
,
pubmed-author:YajimaAA
,
pubmed-author:YamanakaMM
,
pubmed-author:YanagidaKK
pubmed:issnType
Print
pubmed:volume
25
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
373-9
pubmed:dateRevised
2004-11-17
pubmed:meshHeading
pubmed-meshheading:10680333-Adult
,
pubmed-meshheading:10680333-Amniocentesis
,
pubmed-meshheading:10680333-Asian Continental Ancestry Group
,
pubmed-meshheading:10680333-Chromosomes, Human, Pair 13
,
pubmed-meshheading:10680333-Chromosomes, Human, Pair 18
,
pubmed-meshheading:10680333-Down Syndrome
,
pubmed-meshheading:10680333-Female
,
pubmed-meshheading:10680333-Genetic Counseling
,
pubmed-meshheading:10680333-Humans
,
pubmed-meshheading:10680333-Japan
,
pubmed-meshheading:10680333-Karyotyping
,
pubmed-meshheading:10680333-Maternal Age
,
pubmed-meshheading:10680333-Mosaicism
,
pubmed-meshheading:10680333-Pedigree
,
pubmed-meshheading:10680333-Pregnancy
,
pubmed-meshheading:10680333-Pregnancy Trimester, Second
,
pubmed-meshheading:10680333-Recurrence
,
pubmed-meshheading:10680333-Retrospective Studies
,
pubmed-meshheading:10680333-Risk Factors
,
pubmed-meshheading:10680333-Trisomy
,
pubmed-meshheading:10680333-X Chromosome
pubmed:year
1999
pubmed:articleTitle
Risk of recurrence of fetal chromosomal aberrations: analysis of trisomy 21, trisomy 18, trisomy 13, and 45,X in 1,076 Japanese mothers.
pubmed:affiliation
Department of Obstetrics and Gynecology, Tohoku University School of Medicine, Sendai, Japan.
pubmed:publicationType
Journal Article