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Array-based molecular karyotyping in 115 VATER/VACTERL and VATER/VACTERL-like patients identifies disease-causing copy number variations.
- Published in:
- Birth Defects Research, 2017, v. 109, p. 1063, doi. 10.1002/bdr2.1042
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Array-based molecular karyotyping in 115 VATER/VACTERL and VATER/VACTERL-like patients identifies disease-causing copy number variations.
- Published in:
- Birth Defects Research, 2017, v. 109, n. 13, p. 1063, doi. 10.1002/bdr2.1042
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- Publication type:
- Article