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Recurrent In Vitro Fertilization Failure Evaluated by Fluorescence In Situ Hybridization: A Case Report

✍ Scribed by M Grossmann M.S.; J.M Calafell Ph.D.; V Moreno Ph.D.; ; J Balasch M.D.; ; J.A Vanrell M.D.; ; J Egozcue M.D.; ; J Santaló Ph.D.; ; Francesca Vidal Ph.D.


Book ID
119421817
Publisher
Elsevier Science
Year
1998
Tongue
English
Weight
43 KB
Volume
69
Category
Article
ISSN
1556-5653

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We report on a newborn infant with multiple congenital anomalies and apparent nonmosaic trisomy 9 in the blood (by conventional cytogenetic studies) who died shortly after birth. Clinical observations at birth and autopsy are compared with phenotypes of mosaic and nonmosaic trisomy 9 cases reported