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FAMILIAL SARCOIDOSIS WITH MULTIPLE OCCURRENCES IN ELEVEN FAMILIES: A POSSIBLE MECHANISM OF INHERITANCE

✍ Scribed by Verle E. Headings; Denise Weston; Roscoe C. Young Jr.; Robert L. Hackney Jr.


Book ID
114882556
Publisher
John Wiley and Sons
Year
1976
Tongue
English
Weight
507 KB
Volume
278
Category
Article
ISSN
0890-6564

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comprises mental retardation, craniosynostosis, congenital microcephaly, growth failure, glaucoma, congenital heart anomalies, and gastrointestinal defects, e.g., diaphragmatic hernia. It was first described by Lowry and Maclean [1977] in a female patient with Crouzon-like facial anomalies and other