Search Results - DEMIRYILMAZ, F

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  1. 1
    MEFV gene compound heterozygous mutations in familial Mediterranean fever phenotype: a retrospective clinical and molecular study

    MEFV gene compound heterozygous mutations in familial Mediterranean fever phenotype: a retrospective clinical and molecular study by Caglayan, Ahmet Okay, Demiryilmaz, Fatma, Ozyazgan, Isilay, Gumus, Hakan

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  2. 2
    An autosomal recessive adducted thumb‐club foot syndrome observed in Turkish cousins

    An autosomal recessive adducted thumb‐club foot syndrome observed in Turkish cousins by Dundar, Munis, Demiryilmaz, Fatma, Demiryilmaz, Ilhan, Kumandas, Sefer, Erkilic, Kuddusi, Kendirci, Mustafa, Tuncel, Mehmet, Ozyazgan, Isilay, Tolmie, John L

    Published in Clinical genetics
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  3. 3
    Congenital alacrima in a patient with G (Opitz Frias) syndrome

    Congenital alacrima in a patient with G (Opitz Frias) syndrome by DUNDAR, M, ERKILIC, K, DEMIRYILMAZ, F, KÜCÜKAYDIN, M, KENDIRCI, M, OKUR, H, KAZEZ, A

    Published in Human genetics
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  4. 4
    A case of ambiguous genitalia presenting with a 45,X/46,Xr(Y)(p11.2;q11.23)/47,X,idic(Y)(p11.2),idic(Y)(p11.2) karyotype

    A case of ambiguous genitalia presenting with a 45,X/46,Xr(Y)(p11.2;q11.23)/47,X,idic(Y)(p11.2),idic(Y)(p11.2) karyotype by Dundar, Munis, Lowther, Gordon, Acar, Hasan, Kurtoglu, Selim, Demiryilmaz, Fatma, Kucukaydin, Mustafa

    Published in Annales de génétique
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