Found: 4
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Severe craniosynostosis in an infant with deletion 22q11.2 syndrome.
- Published in:
- American Journal of Medical Genetics. Part A, 2013, v. 161A, n. 1, p. 153, doi. 10.1002/ajmg.a.35491
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- Publication type:
- Article
Canadian College of Medical Geneticists guidelines for the indications, analysis, and reporting of cancer specimens.
- Published in:
- Current Oncology, 2011, v. 18, n. 5, p. e250, doi. 10.3747/co.v18i5.775
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- Publication type:
- Article
CCMG guidelines: prenatal and postnatal diagnostic testing for uniparental disomy.
- Published in:
- Clinical Genetics, 2011, v. 79, n. 2, p. 118, doi. 10.1111/j.1399-0004.2010.01547.x
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- Publication type:
- Article
Isodicentric Yp: prenatal diagnosis and outcome in 12 cases.
- Published in:
- Prenatal Diagnosis, 2006, v. 26, n. 4, p. 324, doi. 10.1002/pd.1406
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- Publication type:
- Article