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Schinzel's syndrome II


Associated persons:
Albert A. G. L. Schinzel

Description:
A familiar syndrome of ulnar ray defects, hand abnormalities, microgentialism, delayed puberty, obesity, and anal atresia. Inheritance is autosomal dominant.
Bibliography:
  • S. A. Temtamy, V. A. McKusick:
    The Genetics of Hand Malformations.
    Birth Defects Original Article Series, Volume 14. 619 pages. New York: Alan R. Liss, Inc., 1978.

 
 

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