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Severe midline fusion defects in a newborn with 10q26----qter deletion
J P Fryns1, A Kleczkowska, H Fivez
1Centre for Human Genetics, U.Z. Gasthuisberg, Belgium.
Annales De Genetique
|January 1, 1989
Abstract:
In this report we describe a male newborn with a severe midline fusion syndrome associated with a "pure" distal 10q deletion (del(10)(q26.1----qter].