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Urinary phenylacetylglutamine as dosing biomarker for patients with urea cycle disorders.
Mol Genet Metab. 2012 Nov;107(3):308-14. doi: 10.1016/j.ymgme.2012.08.006. Epub 2012 Aug 18.
Mol Genet Metab. 2012.
PMID: 22958974
Free PMC article.
Clinical Trial.
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.
Gu J, Sreenath Nagamani SC, Hopwood VL, Sanchez B, Saeidinejad Y, Ou Z, Peacock S, Grange DK, Stankiewicz P, Cheung SW.
Gu J, et al. Among authors: sreenath nagamani sc.
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.
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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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