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Complex genomic rearrangement of chromosome 16p13.3 detected by array comparative genomic hybridization in a patient with multiple congenital anomalies, dysmorphic craniofacial features, and developmental delay.
Am J Med Genet A. 2011 Oct;155A(10):2589-92. doi: 10.1002/ajmg.a.34185. Epub 2011 Sep 9.
Am J Med Genet A. 2011.
PMID: 21910221
No abstract available.
Hereditary hemorrhagic telangiectasia with inherited thrombophilia.
Sreenath Nagamani SC, Kundranda MN, Daw HA.
Sreenath Nagamani SC, et al.
Eur J Intern Med. 2006 Jul;17(4):304. doi: 10.1016/j.ejim.2005.12.007.
Eur J Intern Med. 2006.
PMID: 16762788
No abstract available.
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