Search Results - Vn, Ninis

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  1. 1
    Is the novel SCKL3 at 14q23 the predominant Seckel locus?

    Is the novel SCKL3 at 14q23 the predominant Seckel locus? by Mo, Kılınç, Vn, Ninis, Sa, Uğur, B, Tüysüz, M, Seven, S, Balcı, J, Goodship, A, Tolun

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  2. 2
    High frequency of T9 and CFTR mutations in children with idiopathic bronchiectasis

    High frequency of T9 and CFTR mutations in children with idiopathic bronchiectasis by Ninis, V N, Kýlýnç, M O, Kandemir, M, Daðlý, E, Tolun, A

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  3. 3
    Erratum: Is the novel SCKL3 at 14q23 the predominant Seckel locus?

    Erratum: Is the novel SCKL3 at 14q23 the predominant Seckel locus? by MO, Kılınç, VN, Ninis, SA, Uğur, B, Tüysüz, M, Seven, S, Balcı, J, Goodship, A, Tolun

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  4. 4
    Genotype-phenotype correlation in three homozygotes and nine compound heterozygotes for the cystic fibrosis mutation 2183AA→G shows a severe phenotype

    Genotype-phenotype correlation in three homozygotes and nine compound heterozygotes for the cystic fibrosis mutation 2183AA→G shows a severe phenotype by KILINÇ, M O, NINIS, V N, TOLUN, A, ESTIVILL, X, CASALS, T, SAVOV, A, DAGLI, E, KARAKOÇ, F, DEMIRKOL, M, HÜNER, G, ÖZKINAY, F, DEMIR, E, SECULI, J L, PENA, J, BOUSONO, C, FERRER-CALVETE, J, CALVO, C, GLOVER, G, KREMENSKI, I

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