Found: 5
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Prenatal diagnosis of mosaic tetrasomy 5p.
- Published in:
- Prenatal Diagnosis, 2001, v. 21, n. 5, p. 351, doi. 10.1002/pd.66
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- Publication type:
- Article
Trisomy 20 mosaicism confirmed in a phenotypically normal liveborn.
- Published in:
- 1989
- By:
- Publication type:
- journal article
A unique de novo interstitial deletion del(17) (q21.3q23) in a phenotypically abnormal infant.
- Published in:
- Clinical Genetics, 1992, v. 41, n. 1, p. 54, doi. 10.1111/j.1399-0004.1992.tb03631.x
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- Publication type:
- Article
A recurrent deletion in the KIT (mast/stem cell growth factor receptor) proto-oncogene is a frequent cause of human piebaldism.
- Published in:
- Human Molecular Genetics, 1993, v. 2, n. 9, p. 1499
- By:
- Publication type:
- Article
A de novo interstitial deletion of chromosome 6 (q22.2q23.1).
- Published in:
- Clinical Genetics, 1988, v. 33, n. 2, p. 65, doi. 10.1111/j.1399-0004.1988.tb03411.x
- By:
- Publication type:
- Article