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Application of fluorescence in situ hybridization techniques in clinical genetics: use of two alphoid repeat probes detecting the centromeres of chromosomes 13 and 21 or chromosomes 14 and 22, respectively

✍ Scribed by S. Kølvraa; J. Koch; N. Gregersen; P. K. A. Jensen; A. L. Jørgensen; K. B. Petersen; K. Rasmussen; L. Bolund


Book ID
115090182
Publisher
John Wiley and Sons
Year
2008
Tongue
English
Weight
688 KB
Volume
39
Category
Article
ISSN
0009-9163

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