Hirschsprung disease in an infant with a contiguous gene syndrome of chromosome 13
Author:
Publisher
Wiley
Subject
Genetics(clinical)
Reference22 articles.
1. Double Heterozygosity for a RET Substitution Interfering with Splicing and an EDNRB Missense Mutation in Hirschsprung Disease
2. 1992. Nelson textbook of pediatrics, 14th ed. Philadelphia: WB Saunders. p 954-956.
3. A case of Hirschsprung disease with a chromosome 13 microdeletion, del(13)(q32.3q33.2): potential mapping of one disease locus
4. Frequency of 13q Abnormalities Among 203 Patients With Retinoblastoma
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