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Identification of an unbalanced X-autosome translocation by array CGH in a boy with a syndromic form of chondrodysplasia punctata brachytelephalangic type

✍ Scribed by Björn Menten; Karen Buysse; Jo Vandesompele; Els De Smet; Anne De Paepe; Frank Speleman; Geert Mortier


Book ID
116432802
Publisher
Elsevier Science
Year
2005
Tongue
English
Weight
862 KB
Volume
48
Category
Article
ISSN
1769-7212

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