| The acardiac anomaly new case reports and current status. | |
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MedLine Citation:
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PMID: 575694 Owner: NLM Status: MEDLINE |
Abstract/OtherAbstract:
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Two cases of holoacardius are presented. Both had a normal 46,XX female karyotype, identical to that of their respective cotwin. Data are presented supporting the concept that the placental vascular anastomoses are the primary agents in the formation of an acardiac. Cytogenetics, epidemiology and other theories of pathogenesis are discussed. |
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Authors:
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C Kaplan; K Benirschke |
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Publication Detail:
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Type: Case Reports; Journal Article |
Journal Detail:
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Title: Acta geneticae medicae et gemellologiae Volume: 28 ISSN: 0001-5660 ISO Abbreviation: Acta Genet Med Gemellol (Roma) Publication Date: 1979 |
Date Detail:
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Created Date: 1980-07-26 Completed Date: 1980-07-26 Revised Date: 2004-11-17 |
Medline Journal Info:
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Nlm Unique ID: 0370314 Medline TA: Acta Genet Med Gemellol (Roma) Country: ITALY |
Other Details:
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Languages: eng Pagination: 51-9 Citation Subset: IM |
Export Citation:
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APA/MLA Format Download EndNote Download BibTex |
| MeSH Terms | |
Descriptor/Qualifier:
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Cells, Cultured Chromosomes, Human Female Heart Defects, Congenital / genetics*, pathology Humans Infant, Newborn Karyotyping Lymphocytes / ultrastructure Pregnancy Twins* Twins, Monozygotic* |
From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine
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