Deletions of 9q21.3 including NTRK2 are associated with severe phenotype
- PMID: 25348648
- DOI: 10.1002/ajmg.a.36797
Deletions of 9q21.3 including NTRK2 are associated with severe phenotype
Comment on
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Novel interstitial 2.6 Mb deletion on 9q21 associated with multiple congenital anomalies.Am J Med Genet A. 2014 Jan;164A(1):237-42. doi: 10.1002/ajmg.a.36230. Am J Med Genet A. 2014. PMID: 24501764
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