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Unusual scarcity of restriction site polymorphism in the human thyroglobulin gene. A linkage study suggesting autosomal dominance of a defective thyroglobulin allele

✍ Scribed by Frank Baas; Hennie Bikker; Gert-Jan B. Ommen; Jan J. M. Vijlder


Book ID
104707295
Publisher
Springer
Year
1984
Tongue
English
Weight
545 KB
Volume
67
Category
Article
ISSN
0340-6717

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