Fluorescent In Situ Hybridization: Use of Whole Chromosome Paint Probes to Identify Unbalanced Chromosome Translocations

Author:

KRAKER WILLIAM J.,BORELL THOMAS J.,SCHAD CHRISTOPHER R.,PENNINGTON MARY JANE,KARNES PAMELA S.,DEWALD GORDON W.,JENKINS ROBERT B.

Publisher

Elsevier BV

Subject

General Medicine

Reference8 articles.

1. Modern methods of chromosome analysis and their application in clinical practice;Dewald;Clin Lab Annu,1983

2. Use of fluorescent in situ hybridization for marker chromosome identification in congenital and neoplastic disorders;Schad;Am J Clin Pathol,1991

3. Demonstration of gene dosage effects for AK3 and GALT in fibroblasts from a fetus with 9p trisomy;Steinbach;Hum Genet,1983

4. Prenatal diagnosis of an inherited translocation between chromosomes No. 9 and 18;Ebbin;J Med Genet,1973

5. Clinical Atlas of Human Chromosomes;De Grouchy,1984

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