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A 0.7 Mb de novo duplication at 7q21.3 including the genes DLX5 and DLX6 in a patient with split-hand/split-foot malformation.
Am J Med Genet A. 2012 Dec;158A(12):3201-6. doi: 10.1002/ajmg.a.35644. Epub 2012 Nov 20.
Am J Med Genet A. 2012.
PMID: 23169702
Delivery and management of a preterm infant in the burn unit: a multidisciplinary approach.
Rodriguez O, Cooma R, Cooper M, Roth P.
Rodriguez O, et al. Among authors: cooma r.
Burns. 2015 May;41(3):e51-5. doi: 10.1016/j.burns.2015.01.018. Epub 2015 Feb 19.
Burns. 2015.
PMID: 25704835
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Neonatal Gaucher disease presenting as persistent thrombocytopenia.
Roth P, Sklower Brooks S, Potaznik D, Cooma R, Sahdev S.
Roth P, et al. Among authors: cooma r.
J Perinatol. 2005 May;25(5):356-8. doi: 10.1038/sj.jp.7211262.
J Perinatol. 2005.
PMID: 15861202
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