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Title: Alagille syndrome (arteriohepatic dysplasia) and del(20)(p11.2)
Authors: Legius, Eric ×
Fryns, Jean-Pierre
Eyskens, Benedicte
Eggermont, Ephrem
Desmet, Valeer
de Bethune, G
Van den Berghe, Herman #
Issue Date: Apr-1990
Series Title: American Journal of Medical Genetics vol:35 issue:4 pages:532-5
Abstract: 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,del(20)(p11.2) chromosome constitution. This is the second report of a del(20p) in a patient with Alagille syndrome. The possible localisation of this autosomal dominant syndrome on 20p is discussed.
ISSN: 0148-7299
Publication status: published
KU Leuven publication type: IT
Appears in Collections:Clinical Genetics Section (-)
Faculty of Medicine - miscellaneous
Translational Cell & Tissue Research
Cardiovascular Developmental Biology
Department of Human Genetics - miscellaneous
× corresponding author
# (joint) last author

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