Similar articles for PMID: 19138872

Year	Number of Results
1973	1
1976	1
1981	1
1982	1
1983	4
1984	2
1985	4
1986	7
1987	2
1988	5
1989	5
1990	5
1991	5
1992	5
1993	10
1994	3
1995	8
1996	10
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1998	8
1999	6
2000	5
2001	2
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2003	6
2004	4
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2007	9
2008	5
2009	10
2010	14
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2013	9
2014	10
2015	12
2016	5
2017	6
2018	11
2019	4
2020	12
2021	12
2022	9
2023	2
2024	0

1

High-frequency detection of deletions and variable rearrangements at the ornithine transcarbamylase (OTC) locus by oligonucleotide array CGH.

Shchelochkov OA, Li FY, Geraghty MT, Gallagher RC, Van Hove JL, Lichter-Konecki U, Fernhoff PM, Copeland S, Reimschisel T, Cederbaum S, Lee B, Chinault AC, Wong LJ. Shchelochkov OA, et al. Mol Genet Metab. 2009 Mar;96(3):97-105. doi: 10.1016/j.ymgme.2008.11.167. Epub 2009 Jan 12. Mol Genet Metab. 2009. PMID: 19138872

2

[Analysis of ornithine transcarbamylase gene mutations in three boys affected with late-onset ornithine transcarbamylase deficiency].

Chen Z, Wen P, Wang G, Liu X, Chen L, Chen S, Wan L, Cui D, Shang Y, Li C. Chen Z, et al. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2014 Oct;31(5):565-9. doi: 10.3760/cma.j.issn.1003-9406.2014.01.005. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2014. PMID: 25297582 Chinese.

3

An exon 1 deletion in OTC identified using chromosomal microarray analysis in a mother and her two affected deceased newborns: implications for the prenatal diagnosis of ornithine transcarbamylase deficiency.

Quintero-Rivera F, Deignan JL, Peredo J, Grody WW, Crandall B, Sims M, Cederbaum SD. Quintero-Rivera F, et al. Mol Genet Metab. 2010 Dec;101(4):413-6. doi: 10.1016/j.ymgme.2010.08.008. Epub 2010 Aug 14. Mol Genet Metab. 2010. PMID: 20817516

4

Mutation analysis of the ornithine transcarbamylase (OTC) gene in five Japanese OTC deficiency patients revealed two known and three novel mutations including a deep intronic mutation.

Ogino W, Takeshima Y, Nishiyama A, Okizuka Y, Yagi M, Tsuneishi S, Saiki K, Kugo M, Matsuo M. Ogino W, et al. Kobe J Med Sci. 2007;53(5):229-40. Kobe J Med Sci. 2007. PMID: 18204299 Free article.

5

Lymphocyte mRNA analysis of the ornithine transcarbamylase gene in Italian OTCD male patients and manifesting carriers: identification of novel mutations.

Giorgi M, Morrone A, Donati MA, Ciani F, Bardelli T, Biasucci G, Zammarchi E. Giorgi M, et al. Hum Mutat. 2000 Apr;15(4):380-1. doi: 10.1002/(SICI)1098-1004(200004)15:4<380::AID-HUMU12>3.0.CO;2-Q. Hum Mutat. 2000. PMID: 10737985

6

Identification of seven novel missense mutations, two splice-site mutations, two microdeletions and a polymorphic amino acid substitution in the gene for ornithine transcarbamylase (OTC) in patients with OTC deficiency.

Climent C, Rubio V. Climent C, et al. Hum Mutat. 2002 Feb;19(2):185-6. doi: 10.1002/humu.9011. Hum Mutat. 2002. PMID: 11793483

7

Targeted array CGH as a valuable molecular diagnostic approach: experience in the diagnosis of mitochondrial and metabolic disorders.

Wang J, Zhan H, Li FY, Pursley AN, Schmitt ES, Wong LJ. Wang J, et al. Mol Genet Metab. 2012 Jun;106(2):221-30. doi: 10.1016/j.ymgme.2012.03.005. Epub 2012 Mar 21. Mol Genet Metab. 2012. PMID: 22494545

8

Molecular mechanisms underlying large genomic deletions in ornithine transcarbamylase (OTC) gene.

Quental R, Azevedo L, Rubio V, Diogo L, Amorim A. Quental R, et al. Clin Genet. 2009 May;75(5):457-64. doi: 10.1111/j.1399-0004.2009.01172.x. Clin Genet. 2009. PMID: 19475717

9

Contiguous gene deletion syndrome in a female with ornithine transcarbamylase deficiency.

Balasubramaniam S, Rudduck C, Bennetts B, Peters G, Wilcken B, Ellaway C. Balasubramaniam S, et al. Mol Genet Metab. 2010 Jan;99(1):34-41. doi: 10.1016/j.ymgme.2009.08.007. Mol Genet Metab. 2010. PMID: 19783189

10

Gene Mutation Analysis and Prenatal Diagnosis of the Ornithine Transcarbamylase (OTC) Gene in Two Families with Ornithine Transcarbamylase Deficiency.

Li S, Cai Y, Shi C, Liu M, Liu B, Lin L, Xiao X, Hao H. Li S, et al. Med Sci Monit. 2018 Oct 18;24:7431-7437. doi: 10.12659/MSM.911295. Med Sci Monit. 2018. PMID: 30333473 Free PMC article.

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