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rdf:type |
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lifeskim:mentions |
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pubmed:issue |
4
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pubmed:dateCreated |
2011-1-4
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pubmed:abstractText |
To present prenatal ultrasound findings and molecular diagnosis of microvillus inclusion disease, and to review the literature of abnormal prenatal ultrasound findings associated with congenital diarrhea.
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pubmed:language |
eng
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pubmed:journal |
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pubmed:citationSubset |
IM
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pubmed:chemical |
|
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pubmed:status |
MEDLINE
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pubmed:month |
Dec
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pubmed:issn |
1875-6263
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pubmed:author |
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pubmed:copyrightInfo |
Copyright © 2010 Taiwan Association of Obstetric & Gynecology. Published by Elsevier B.V. All rights reserved.
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pubmed:issnType |
Electronic
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pubmed:volume |
49
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
487-94
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pubmed:dateRevised |
2011-8-24
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pubmed:meshHeading |
pubmed-meshheading:21199752-Codon, Nonsense,
pubmed-meshheading:21199752-Colon,
pubmed-meshheading:21199752-DNA Mutational Analysis,
pubmed-meshheading:21199752-Fathers,
pubmed-meshheading:21199752-Female,
pubmed-meshheading:21199752-Fetal Diseases,
pubmed-meshheading:21199752-Genetic Counseling,
pubmed-meshheading:21199752-Humans,
pubmed-meshheading:21199752-Inclusion Bodies,
pubmed-meshheading:21199752-Infant, Newborn,
pubmed-meshheading:21199752-Karyotyping,
pubmed-meshheading:21199752-Malabsorption Syndromes,
pubmed-meshheading:21199752-Male,
pubmed-meshheading:21199752-Microvilli,
pubmed-meshheading:21199752-Mothers,
pubmed-meshheading:21199752-Mucolipidoses,
pubmed-meshheading:21199752-Pedigree,
pubmed-meshheading:21199752-Polyhydramnios,
pubmed-meshheading:21199752-Pregnancy,
pubmed-meshheading:21199752-Ultrasonography, Prenatal
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pubmed:year |
2010
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pubmed:articleTitle |
Microvillus inclusion disease: prenatal ultrasound findings, molecular diagnosis and genetic counseling of congenital diarrhea.
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pubmed:affiliation |
Department of Obstetrics and Gynecology, Mackay Memorial Hospital, Tao-Yuan, Taiwan. cpc_mmh@yahoo.com
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pubmed:publicationType |
Journal Article,
Case Reports,
Research Support, Non-U.S. Gov't
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