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18925617
Source:
http://linkedlifedata.com/resource/pubmed/id/18925617
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59
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Statements in which the resource exists as a subject.
Predicate
Object
rdf:type
pubmed:Citation
lifeskim:mentions
umls-concept:C0000768
,
umls-concept:C0011923
,
umls-concept:C0015965
,
umls-concept:C0024554
,
umls-concept:C0033053
,
umls-concept:C0043292
,
umls-concept:C0205108
,
umls-concept:C0205245
,
umls-concept:C0426857
,
umls-concept:C0444930
,
umls-concept:C0678804
,
umls-concept:C1116439
,
umls-concept:C1515568
,
umls-concept:C1520175
,
umls-concept:C1522538
,
umls-concept:C1538631
,
umls-concept:C1825005
pubmed:issue
11
pubmed:dateCreated
2008-11-5
pubmed:language
eng
pubmed:journal
http://linkedlifedata.com/resource/pubmed/journal/8106540
pubmed:citationSubset
IM
pubmed:status
MEDLINE
pubmed:month
Nov
pubmed:issn
0197-3851
pubmed:author
pubmed-author:GhoshAA
,
pubmed-author:HigginsLL
,
pubmed-author:KilbyM DMD
,
pubmed-author:LarkinsS ASA
,
pubmed-author:MartinW LWL
,
pubmed-author:MillerCC
,
pubmed-author:OstojicNN
pubmed:issnType
Print
pubmed:volume
28
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
1068-71
pubmed:meshHeading
pubmed-meshheading:18925617-Abortion, Induced
,
pubmed-meshheading:18925617-Chromosomes, Human, Pair 22
,
pubmed-meshheading:18925617-Chromosomes, Human, X
,
pubmed-meshheading:18925617-Chromosomes, Human, Y
,
pubmed-meshheading:18925617-Female
,
pubmed-meshheading:18925617-Genetic Counseling
,
pubmed-meshheading:18925617-Heart Ventricles
,
pubmed-meshheading:18925617-Humans
,
pubmed-meshheading:18925617-Karyotyping
,
pubmed-meshheading:18925617-Magnetic Resonance Imaging
,
pubmed-meshheading:18925617-Male
,
pubmed-meshheading:18925617-Pregnancy
,
pubmed-meshheading:18925617-Pregnancy Trimester, Second
,
pubmed-meshheading:18925617-Prenatal Diagnosis
,
pubmed-meshheading:18925617-Sequence Deletion
,
pubmed-meshheading:18925617-Sex Chromosome Aberrations
,
pubmed-meshheading:18925617-Uniparental Disomy
pubmed:year
2008
pubmed:articleTitle
Prenatal diagnosis and prenatal imaging of a de novo 46,X,der(Y)t(X;Y)(p22.13;q11.23) leading to functional disomy for the distal end of the X chromosome short arm from Xp22.13 in a phenotypically male fetus with posterior fossa abnormalities.
pubmed:publicationType
Letter
,
Case Reports