Search Results - "Gumus, Dilihan"

Comparative genome hybridization suggests a role for NRXN1 and APBA2 in schizophrenia by Kirov, George, Gumus, Dilihan, Chen, Wei, Norton, Nadine, Georgieva, Lyudmila, Sari, Murat, O’Donovan, Michael C, Erdogan, Fikret, Owen, Michael J, Ropers, Hans-Hilger, Ullmann, Reinhard

“…Copy number variations (CNVs) account for a substantial proportion of human genomic variation, and have been shown to cause neurodevelopmental disorders. We…”
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Subtelomeric 6p monosomy and 12q trisomy in a patient with a 46,XX,der(6)t(6;12)(p25.3;q24.31) karyotype: Phenotypic overlap with Mutchinick syndrome by Semerci, C. Nur, Cinbis, Mine, Ullmann, Reinhard, Steininger, Anne, Bahce, Muhterem, Yagci, Baki, Ozden, Serap, Sabir, Nuran, Gumus, Dilihan, Tepeli, Emre, Arteaga, Jazmín, Mutchinick, Osvaldo M.

“…We report on a patient with partial monosomy 6p and partial trisomy 12q identified by fluorescent in situ hybridization (FISH) and array‐based comparative…”
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Subtelomeric 6p monosomy and 12q trisomy in a patient with a 46,XX,der(6)t(6;12)(p25.3;q24.31) karyotype: Phenotypic overlap with Mutchinick syndrome by Semerci, C. Nur, Cinbis, Mine, Ullmann, Reinhard, Steininger, Anne, Bahce, Muhterem, Yagci, Baki, Ozden, Serap, Sabir, Nuran, Gumus, Dilihan, Tepeli, Emre, Arteaga, Jazmín, Mutchinick, Osvaldo M.

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Sister chromatid exchange frequency in lymphocytes cultured from cotton gin workers by AÇIKBAŞ, İbrahim, DÜZCAN, Füsun, BAĞCI, Hüseyin, ATMACA, Münevver, GÜMÜŞ, Dilihan

“…Genetic biomonitoring of human populations exposed to potential mutagens/carcinogens can be performed using different genetic markers. Sister chromatid…”
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