{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2025,10,19]],"date-time":"2025-10-19T20:48:51Z","timestamp":1760906931554},"reference-count":16,"publisher":"Wiley","issue":"6","license":[{"start":{"date-parts":[[2005,11,21]],"date-time":"2005-11-21T00:00:00Z","timestamp":1132531200000},"content-version":"vor","delay-in-days":4921,"URL":"http:\/\/onlinelibrary.wiley.com\/termsAndConditions#vor"}],"content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":["Prenatal Diagnosis"],"published-print":{"date-parts":[[1992,6]]},"abstract":"<jats:title>Abstract<\/jats:title><jats:p>A case of mosaic tetrasomy 12p was detected in amniotic fluid cell cultures from a 28\u2010year\u2010old woman referred to us at 26 weeks' gestation because of hydramnios. The fetus was shown on ultrasonography to have an omphalocele and a short femur length. Labour was induced at 32 weeks. An infant with multiple congenital anomalies was delivered and died after 10 min. The diagnosis of i(12p) or Pallister\u2010Killian syndrome was confirmed cytogenetically in fibroblast and lymphocyte cultures. Increased <jats:bold>LDH\u2010B<\/jats:bold> activity was demonstrated in fibroblasts.<\/jats:p>","DOI":"10.1002\/pd.1970120608","type":"journal-article","created":{"date-parts":[[2007,3,4]],"date-time":"2007-03-04T06:15:32Z","timestamp":1172988932000},"page":"529-534","source":"Crossref","is-referenced-by-count":17,"title":["A further prenatal diagnosis of mosaic tetrasomy 12p (Pallister\u2010Killian syndrome)"],"prefix":"10.1002","volume":"12","author":[{"given":"M. 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