Publisher
Springer Berlin Heidelberg
Reference42 articles.
1. Abid F, Tardy V, Gaouzi A, El Hessni A, Morel Y, Chabraoui L (2008) CYP21A2 gene mutation analysis in Moroccan patients with classic form of 21-hydroxylase deficiency: high regional prevalence of p.Q318X mutation and identification of a novel p.L353R mutation. Clin Chem Lab Med 46(12):1707–1713
2. Aboussair N, Berahou A, Perrault I, Elalaoui SC, Megzari A, Rozet JM, Kaplan J, Sefiani A (2010) First North African observation of Leber congenital amaurosis secondary to CEP290 gene mutation. J Fr Ophtalmol (in press)
3. Ainahi A, Kebbou M, Timinouni M, Benabdeljalil N, Fechtali T, Oufara S, El Antri S (2006) Study of the RET gene and his implication in thyroid cancer: Morocco case family. Indian J Cancer 43:122–126
4. Alif N, Hess K, Straczek J, Sebbar S, Belahsen Y, Mouane N, Abkari A, Nabet P, Gelot MA (2000) Mucopolysaccharidosis type I in Morocco: clinical features and genetic profile. Arch Pediatr 7(6):597–604
5. Allamand V, Guicheney P (2002) Merosin-deficient congenital muscular dystrophy, autosomal recessive (MDC1A, MIM#156225, LAMA2 gene coding for alpha2 chain of laminin). Eur J Hum Genet 10(2):91–94
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