We report on a boy with Alagille syndrome. Chromosome analysis on a peripheral blood lymphocyte culture showed a de novo deletion of the short arm of chromosome 20 with a 46,XY,de1(20)(p11.2) chromosome constitution. This is the second report of a del(2Op) in a patient with Alagille syndrome. The po
โฆ LIBER โฆ
Alagille syndrome (arteriohepatic dysplasia)
โ Scribed by Giuseppe Santoro; Roberto Formigari; Luigi Ballerini
- Book ID
- 115660468
- Publisher
- Elsevier Science
- Year
- 1995
- Tongue
- English
- Weight
- 125 KB
- Volume
- 130
- Category
- Article
- ISSN
- 1097-6744
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