Tajir M - Search Results

1

Germline mosaicism in Rubinstein-Taybi syndrome.

Tajir M, Fergelot P, Lancelot G, Elalaoui SC, Arveiler B, Lacombe D, Sefiani A. Tajir M, et al. Gene. 2013 Apr 15;518(2):476-8. doi: 10.1016/j.gene.2012.12.105. Epub 2013 Jan 23. Gene. 2013. PMID: 23352794

2

Frequency of IL28B rs12979860 single-nucleotide polymorphism alleles in newborn infants and in patients with chronic hepatitis C in Morocco.

Tajir M, Elmachad M, Kabbaj N, Laarabi FZ, Barkat A, Amrani N, Sefiani A. Tajir M, et al. Genet Test Mol Biomarkers. 2012 Aug;16(8):981-3. doi: 10.1089/gtmb.2011.0353. Epub 2012 Apr 17. Genet Test Mol Biomarkers. 2012. PMID: 22509814

3

Pyruvate dehydrogenase deficiency caused by a new mutation of PDHX gene in two Moroccan patients.

Tajir M, Arnoux JB, Boutron A, Elalaoui SC, De Lonlay P, Sefiani A, Brivet M. Tajir M, et al. Eur J Med Genet. 2012 Oct;55(10):535-40. doi: 10.1016/j.ejmg.2012.06.006. Epub 2012 Jul 20. Eur J Med Genet. 2012. PMID: 22766002

4

An inherited LMNA gene mutation in atypical Progeria syndrome.

Doubaj Y, De Sandre-Giovannoli A, Vera EV, Navarro CL, Elalaoui SC, Tajir M, Lévy N, Sefiani A. Doubaj Y, et al. Among authors: tajir m. Am J Med Genet A. 2012 Nov;158A(11):2881-7. doi: 10.1002/ajmg.a.35557. Epub 2012 Sep 18. Am J Med Genet A. 2012. PMID: 22991222

5

[Costello syndrome: report of a case].

Tajir M, Fergelot P, Lancelot G, Arveiler B, Elalaoui SC, Lacombe D, Sefiani A. Tajir M, et al. Pan Afr Med J. 2012;12:64. Epub 2012 Jul 4. Pan Afr Med J. 2012. PMID: 23024823 Free PMC article. French.

6

[Prenatal diagnosis of trisomy 21 by fluorescence in situ hybridization (FISH): about the first tests in Morocco].

Lamzouri A, Natiq A, Tajir M, Sendid M, Sefiani A. Lamzouri A, et al. Among authors: tajir m. Pan Afr Med J. 2012;13:38. Epub 2012 Oct 22. Pan Afr Med J. 2012. PMID: 23330029 Free PMC article. French.

7

Autosomal-recessive SASH1 variants associated with a new genodermatosis with pigmentation defects, palmoplantar keratoderma and skin carcinoma.

Courcet JB, Elalaoui SC, Duplomb L, Tajir M, Rivière JB, Thevenon J, Gigot N, Marle N, Aral B, Duffourd Y, Sarasin A, Naim V, Courcet-Degrolard E, Aubriot-Lorton MH, Martin L, Abrid JE, Thauvin C, Sefiani A, Vabres P, Faivre L. Courcet JB, et al. Among authors: tajir m. Eur J Hum Genet. 2015 Jul;23(7):957-62. doi: 10.1038/ejhg.2014.213. Epub 2014 Oct 15. Eur J Hum Genet. 2015. PMID: 25315659 Free PMC article.

8

AGXT Gene Mutations and Prevalence of Primary Hyperoxaluria Type 1 in Moroccan Population.

Boualla L, Tajir M, Oulahiane N, Lyahyai J, Laarabi FZ, Chafai Elalaoui S, Soulami K, Ait Ouamar H, Sefiani A. Boualla L, et al. Among authors: tajir m. Genet Test Mol Biomarkers. 2015 Nov;19(11):623-8. doi: 10.1089/gtmb.2015.0136. Epub 2015 Sep 18. Genet Test Mol Biomarkers. 2015. PMID: 26383609

9

Acromelic frontonasal dysostosis and ZSWIM6 mutation: phenotypic spectrum and mosaicism.

Twigg SR, Ousager LB, Miller KA, Zhou Y, Elalaoui SC, Sefiani A, Bak GS, Hove H, Hansen LK, Fagerberg CR, Tajir M, Wilkie AO. Twigg SR, et al. Among authors: tajir m. Clin Genet. 2016 Sep;90(3):270-5. doi: 10.1111/cge.12721. Epub 2016 Feb 3. Clin Genet. 2016. PMID: 26706854 Free PMC article.

10

Ankyloblepharon-ectodermal Defects-cleft Lip-palate Syndrome Due to a Novel Missense Mutation in the SAM Domain of the TP63 Gene.

Tajir M, Lyahyai J, Guaoua S, El Alloussi M, Sefiani A. Tajir M, et al. Balkan J Med Genet. 2020 Aug 26;23(1):95-98. doi: 10.2478/bjmg-2020-0013. eCollection 2020 Jun. Balkan J Med Genet. 2020. PMID: 32953416 Free PMC article.

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