{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2023,10,23]],"date-time":"2023-10-23T09:14:55Z","timestamp":1698052495904},"reference-count":10,"publisher":"Wiley","issue":"11","license":[{"start":{"date-parts":[[2005,11,21]],"date-time":"2005-11-21T00:00:00Z","timestamp":1132531200000},"content-version":"vor","delay-in-days":4768,"URL":"http:\/\/onlinelibrary.wiley.com\/termsAndConditions#vor"}],"content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":["Prenatal Diagnosis"],"published-print":{"date-parts":[[1992,11]]},"abstract":"<jats:title>Abstract<\/jats:title><jats:p>This study describes three couples a t risk for homozygous \u03b2\u2010thalassaemia in which one of the partners carried a short deletion \u03b2\u2010thalassaemia defect. Detection of short deletions in trophoblast DNA was accomplished by the very simple procedure of non\u2010denaturing polyacrylamide gel electrophoresis. 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