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Congenital Heart Disease: Molecular Diagnostics - Methods in Molecular Medicine Mary Kearns-jonker 2006 edition
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Pieejams arī kā:
Congenital Heart Disease: Molecular Diagnostics - Methods in Molecular Medicine
Mary Kearns-jonker
In particular, the methods can be used to identify in clinical samples those genetic mutations responsible for such congenital abnormalities as Marfan syndrome, Williams-Beuren Syndrome, Alagille syndrome, Noonan syndrome, and Friedreich ataxia.
278 pages, biography
| Mediji | Grāmatas Paperback Book (Grāmata ar mīksto vāku un līmēto muguru) |
| Izlaists | 2014. gada 20. oktobris |
| ISBN13 | 9781627038560 |
| Izdevēji | Humana Press Inc. |
| Lapas | 278 |
| Izmēri | 155 × 235 × 15 mm · 450 g |
| Valoda | Angļu |
| Redaktors | Kearns-Jonker, Mary |
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