Skip to main content
Garrison-Morton-Norman
History of Medicine
Subject
Facets
Author
Entry #
Year
Place
About Us
Contact
Search the corpus
Home
/
Clinical Specialties & Practice › GENETICS / HEREDITY › HEREDITARY / CONGENITAL DISEASES OR DISORDERS › Waardenburg Syndrome
Waardenburg Syndrome
Exhibiting 1 entries found in the GMN corpus.
Sort by Year
Sort by Author
Year
Title & Tags
Author(s)
1951 CE
A new syndrome combining developmental anomalies of the eyelids, eyebrows and nose root with pigmentary defects of the iris and head hair with congenital deafness.
Ancient
ENT & Hearing
Genetics & Heredity
WAARDENBURG, Petrus Johannes (1886 – 1979)
Browse Index:
Subjects
Facets
Authors
Entry Numbers
Years
Places
Introduction
Director's Advisory Board
Contact
