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Utility of whole-genome sequencing for detection of newborn screening disorders in a population cohort of 1,696 neonates. [electronic resource] by
- Bodian, Dale L
- Klein, Elisabeth
- Iyer, Ramaswamy K
- Wong, Wendy S W
- Kothiyal, Prachi
- Stauffer, Daniel
- Huddleston, Kathi C
- Gaither, Amber D
- Remsburg, Irina
- Khromykh, Alina
- Baker, Robin L
- Maxwell, George L
- Vockley, Joseph G
- Niederhuber, John E
- Solomon, Benjamin D
Producer: 20161110
In:
Genetics in medicine : official journal of the American College of Medical Genetics vol. 18
Availability: No items available.
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