Chromosome 11q13 deletion syndrome
Author:
Affiliation:
1. Department of Pediatrics, Korea University College of Medicine, Seoul, Korea.
Publisher
Korean Pediatric Society
Subject
Pediatrics,Pediatrics, Perinatology and Child Health
Link
https://synapse.koreamed.org/pdf/10.3345/kjp.2016.59.11.S10
Reference15 articles.
1. SNP genome scanning localizes oto-dental syndrome to chromosome 11q13 and microdeletions at this locus implicate FGF3 in dental and inner-ear disease and FADD in ocular coloboma
2. Otodental syndrome
3. A Case with Neurosensorial Hearing Loss and Anodonty Findings: Is This a Variant of Otodental Syndrome?
4. Otodental syndrome: A case report and genetic considerations
5. “Otodental” dysplasia
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