Christopher Vlangos

Christopher Vlangos

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Christopher Vlangos

Christopher Vlangos

Publications by authors named "Christopher Vlangos"

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The 24th international Mammalian Genome Conference meeting report.

Mamm Genome 2011 Apr 5;22(3-4):148-55. Epub 2011 Feb 5.

Department of Molecular Biology and Genetics, Cornell University, Ithaca, NY 14850, USA.

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http://dx.doi.org/10.1007/s00335-011-9314-xDOI Listing
April 2011

Tom1l2 hypomorphic mice exhibit increased incidence of infections and tumors and abnormal immunologic response.

Mamm Genome 2008 Apr 15;19(4):246-62. Epub 2008 Mar 15.

Department of Human Genetics, Medical College of Virginia Campus, Virginia Commonwealth University, Richmond, VA 23298, USA.

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http://dx.doi.org/10.1007/s00335-008-9100-6DOI Listing
April 2008

A milder variant of Pierson syndrome.

Pediatr Nephrol 2008 Feb 18;23(2):323-7. Epub 2007 Oct 18.

Department of Gastroenterology and Nephrology, Orenburg Regional Children's Hospital, Ribakovskaya street 3, 460000, Orenburg, Russia.

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http://dx.doi.org/10.1007/s00467-007-0624-xDOI Listing
February 2008

Smith-Magenis syndrome and Moyamoya disease in a patient with del(17)(p11.2p13.1).

Am J Med Genet A 2007 May;143A(9):999-1008

Department of Human Genetics, Medical College of Virginia Campus, Virginia Commonwealth University, Richmond, VA 23298, USA.

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http://dx.doi.org/10.1002/ajmg.a.31689DOI Listing
May 2007

Mutational analysis of NPHS2 and WT1 in frequently relapsing and steroid-dependent nephrotic syndrome.

Pediatr Nephrol 2007 Apr 10;22(4):509-13. Epub 2007 Jan 10.

Department of Pediatrics, Division of Nephrology, Ann Arbor, MI 48109, USA.

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http://link.springer.com/10.1007/s00467-006-0377-y
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http://dx.doi.org/10.1007/s00467-006-0377-yDOI Listing
April 2007

Genotype-phenotype correlation in Smith-Magenis syndrome: evidence that multiple genes in 17p11.2 contribute to the clinical spectrum.

Genet Med 2006 Jul;8(7):417-27

Department of Human Genetics, Medical College of Virginia Campus, Virginia Commonwealth University, Richmond, Virginia 23298, USA.

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http://dx.doi.org/10.1097/01.gim.0000228215.32110.89DOI Listing
July 2006

Diagnostic FISH probes for del(17)(p11.2p11.2) associated with Smith-Magenis syndrome should contain the RAI1 gene.

Am J Med Genet A 2005 Jan;132A(3):278-82

Genetics Graduate Program, Michigan State University, East Lansing, Michigan, USA.

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http://doi.wiley.com/10.1002/ajmg.a.30461
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http://dx.doi.org/10.1002/ajmg.a.30461DOI Listing
January 2005

Refinement of the Smith-Magenis syndrome critical region to approximately 950kb and assessment of 17p11.2 deletions. Are all deletions created equally?

Mol Genet Metab 2003 Jun;79(2):134-41

Graduate Program in Genetics, Michigan State University, S-320 Plant Biology Building, 178 Wilson Road, East Lansing, MI 48824, USA.

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http://dx.doi.org/10.1016/s1096-7192(03)00048-9DOI Listing
June 2003

Mutations in RAI1 associated with Smith-Magenis syndrome.

Nat Genet 2003 Apr 24;33(4):466-8. Epub 2003 Mar 24.

Genetics Graduate Program, S-320 Plant Biology Building, Michigan State University, East Lansing, Michigan 48823, USA.

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http://dx.doi.org/10.1038/ng1126DOI Listing
April 2003