Abdellatif Errami

Abdellatif Errami

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Abdellatif Errami

Abdellatif Errami

Publications by authors named "Abdellatif Errami"

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18Publications

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Deletions within COL11A1 in Type 2 stickler syndrome detected by multiplex ligation-dependent probe amplification (MLPA).

BMC Med Genet 2013 Apr 26;14:48. Epub 2013 Apr 26.

East Anglian Regional Genetics Laboratory, Addenbrooke's Hospital, Cambridge University Hospitals NHS Trust, Cambridge, UK.

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http://dx.doi.org/10.1186/1471-2350-14-48DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3652776PMC
April 2013

A new case of GABA transaminase deficiency facilitated by proton MR spectroscopy.

J Inherit Metab Dis 2010 Feb 6;33(1):85-90. Epub 2010 Jan 6.

Clinical Research Institute, Kanagawa Children's Medical Center, Minami-ku, Yokohama, Japan.

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http://dx.doi.org/10.1007/s10545-009-9022-9DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2828554PMC
February 2010

MLPA diagnostics of complex microbial communities: relative quantification of bacterial species in oral biofilms.

J Microbiol Methods 2008 Dec 13;75(3):558-65. Epub 2008 Sep 13.

Department of Cariology, Endodontology, Pedodontology, Academic Centre for Dentistry Amsterdam, University of Amsterdam and VU University Amsterdam, The Netherlands.

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http://dx.doi.org/10.1016/j.mimet.2008.08.012DOI Listing
December 2008

Genetic subtyping of Fanconi anemia by comprehensive mutation screening.

Hum Mutat 2008 Jan;29(1):159-66

Department of Clinical Genetics, Vrije Universiteit Medical Center, Amsterdam, The Netherlands.

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http://dx.doi.org/10.1002/humu.20625DOI Listing
January 2008

MS-MLPA: an attractive alternative laboratory assay for robust, reliable, and semiquantitative detection of MGMT promoter hypermethylation in gliomas.

Lab Invest 2007 Oct 13;87(10):1055-65. Epub 2007 Aug 13.

Department of Pathology, Nijmegen Center for Molecular Life Sciences, Radboud University Nijmegen Medical Centre, Nijmegen, The Netherlands.

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http://dx.doi.org/10.1038/labinvest.3700664DOI Listing
October 2007

Fanconi anemia is associated with a defect in the BRCA2 partner PALB2.

Nat Genet 2007 Feb 31;39(2):159-61. Epub 2006 Dec 31.

Dana-Farber Cancer Institute and Harvard Medical School, 44 Binney Street, Boston, Massachusetts 02115, USA.

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http://dx.doi.org/10.1038/ng1942DOI Listing
February 2007

Epigenetic events of disease progression in head and neck squamous cell carcinoma.

Arch Otolaryngol Head Neck Surg 2006 Jun;132(6):668-77

Department of Otolaryngology-Head and Neck Surgery and Research Division, Henry Ford Health System, Detroit, Mich, USA.

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http://dx.doi.org/10.1001/archotol.132.6.668DOI Listing
June 2006

Screening for large mutations of the NF2 gene.

Genes Chromosomes Cancer 2005 Apr;42(4):384-91

Laboratory for Tumor Biology and Malformation, Department of Maxillofacial Surgery, University Hospital Eppendorf, Martinistrasse 52, 20246 Hamburg, Germany.

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http://doi.wiley.com/10.1002/gcc.20138
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http://dx.doi.org/10.1002/gcc.20138DOI Listing
April 2005

Identification of genomic deletions of the APC gene in familial adenomatous polyposis by two independent quantitative techniques.

Genet Test 2004 ;8(3):248-56

Department of Clinical Genetics, Göteborg University, Sahlgrenska University Hospital/Ostra, Göteborg, Sweden.

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http://dx.doi.org/10.1089/gte.2004.8.248DOI Listing
April 2005

A single amino acid substitution in DNA-PKcs explains the novel phenotype of the CHO mutant, XR-C2.

Nucleic Acids Res 2002 Dec;30(23):5120-8

College of Veterinary Medicine, Department of Pathobiology and Diagnostic Investigation, Michigan State University, 350 FST, East Lansing, MI 48824, USA.

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC137947PMC
http://dx.doi.org/10.1093/nar/gkf625DOI Listing
December 2002