## Abstract We report on molecular studies in 7 patients with WolfβHirschhorn syndrome (WHC) not showing an obvious chromosome 4p deletion. Analysis of a set of polymorphic probes mapping in the 4p16.3 region showed the absence of paternal haplotypes in 5 cases, and maternal haplotypes in 2. These
Parental origin of de novo chromosome 9 deletions in del(9p) syndrome
β Scribed by Micale, Mark A. ;Haren, J. Marie ;Conroy, Jeffrey M. ;Crowe, Carol A. ;Schwartz, Stuart
- Publisher
- John Wiley and Sons
- Year
- 1995
- Tongue
- English
- Weight
- 366 KB
- Volume
- 57
- Category
- Article
- ISSN
- 0148-7299
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