Chromosome analysis with high-resolution banding showed a small de novo interstitial deletion of chromosome 2(p21 -p22.2) in an infant with holoprosencephaly. This is the first such observation. There is a well-known association with abnormalities of chromosome 13 (most commonly trisomy 13, but also
Human population studies with cytogenetic biomarkers: Review of the literature and future prospectives
✍ Scribed by Stefano Bonassi; Donatella Ugolini; Micheline Kirsch-Volders; Ulf Strömberg; Roel Vermeulen; James D. Tucker
- Publisher
- John Wiley and Sons
- Year
- 2005
- Tongue
- English
- Weight
- 137 KB
- Volume
- 45
- Category
- Article
- ISSN
- 0893-6692
- DOI
- 10.1002/em.20115
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