https://www.munisdundar.com/pubs/dundar-syndrome/2014-10-01T18:40:34+03:00https://www.munisdundar.com/pubs/analysing-the-role-of-mdm2-snp309-in-patients-with-glioblastoma-multiforme/2014-10-01T19:55:34+03:00https://www.munisdundar.com/pubs/associated-anomalies-in-asymmetric-crying-facies-and-22q11-deletion/2014-10-01T19:56:45+03:00https://www.munisdundar.com/pubs/sacrococcygeal-teratoma-in-a-fetus-with-prenatally-diagnosed-partial-trisomy-10q-10q24-3-qter-and-partial-monosomy-17p-p13-3-pter/2014-10-01T19:58:20+03:00https://www.munisdundar.com/pubs/biotechnology-worldwide-and-the-european-biotechnology-thematic-network-association-ebtna/2014-10-01T20:00:08+03:00https://www.munisdundar.com/pubs/inherited-diseases-and-syndromes-leading-to-aortic-aneurysms-and-dissections/2014-10-01T20:00:55+03:00https://www.munisdundar.com/pubs/idiopathic-hirsutism-local-and-peripheral-expression-of-aromatase-cyp19a-and-5-alpha-reductase-genes-srd5a1-and-srd5a2/2014-10-01T20:02:41+03:00https://www.munisdundar.com/pubs/lack-of-association-between-the-glu298asp-polymorphism-of-endothelial-nitric-oxide-synthase-and-slow-coronary-flow-in-the-turkish-population/2014-10-01T20:03:51+03:00https://www.munisdundar.com/pubs/a-unique-case-of-a-patient-with-partial-trisomy-22-and-lipodystrophy-is-it-a-new-syndrome-due-to-an-igf-ir-mutation/2014-10-01T21:41:49+03:00https://www.munisdundar.com/pubs/holt-oram-syndrome-in-two-generations-with-translocation-t915p12q11-2/2014-10-01T21:42:35+03:00https://www.munisdundar.com/pubs/a-new-syndrome-of-microtia-with-unilateral-renal-agenesis-and-short-stature/2014-10-01T21:43:51+03:00https://www.munisdundar.com/pubs/a-family-with-osteogenesis-imperfecta-frontonasal-dysplasia-ear-abnormality-and-mental-retardation/2014-10-01T21:44:59+03:00https://www.munisdundar.com/pubs/a-case-of-46-xx-t217q37-1q25-with-recurrent-miscarriage/2014-10-01T21:46:06+03:00https://www.munisdundar.com/pubs/etiopathogenesis-of-sheehans-syndrome-roles-of-coagulation-factors-and-tnf-alpha/2014-10-01T21:47:04+03:00https://www.munisdundar.com/pubs/prenatally-detected-de-novo-46-xx-t2121p12p12-at-chorionic-villus-sampling/2014-10-01T21:47:55+03:00https://www.munisdundar.com/pubs/loss-of-dermatan-4-sulfotransferase-1-function-results-in-adducted-thumb-clubfoot-syndrome/2014-10-01T21:48:54+03:00https://www.munisdundar.com/pubs/current-state-of-biotechnology-in-turkey/2014-10-01T21:50:06+03:00https://www.munisdundar.com/pubs/how-the-i1307k-adenomatous-polyposis-coli-gene-variant-contributes-in-the-assessment-of-risk-of-colorectal-cancer-but-not-stomach-cancer-in-a-turkish-population/2014-10-01T21:52:58+03:00https://www.munisdundar.com/pubs/an-autosomal-recessive-adducted-thumb-club-foot-syndrome-observed-in-turkish-cousins/2014-10-01T21:54:46+03:00https://www.munisdundar.com/pubs/common-familial-mediterranean-fever-gene-mutations-in-a-turkish-cohort/2014-10-01T21:55:55+03:00https://www.munisdundar.com/pubs/congenital-alacrima-in-a-patient-with-g-opitz-frias-syndrome/2014-10-01T21:57:23+03:00https://www.munisdundar.com/pubs/the-role-of-tnf-alpha-and-pai-1-gene-polymorphisms-in-familial-mediterranean-fever/2014-10-01T22:02:00+03:00https://www.munisdundar.com/pubs/a-molecular-analysis-of-familial-mediterranean-fever-disease-in-a-cohort-of-turkish-patients/2014-10-01T22:04:55+03:00https://www.munisdundar.com/pubs/unbalanced-322-translocation-with-22q11-and-3p-deletion-syndrome/2014-10-01T22:06:12+03:00https://www.munisdundar.com/pubs/a-case-with-adducted-thumb-and-club-foot-syndrome/2014-10-01T22:06:56+03:00https://www.munisdundar.com/pubs/a-case-with-waardenburg-syndrome-presenting-with-two-separate-translocations-one-reciprocal-and-one-complex/2014-10-01T22:10:24+03:00https://www.munisdundar.com/pubs/frank-ter-haar-syndrome-with-unusual-clinical-features/2014-10-01T22:13:13+03:00https://www.munisdundar.com/pubs/partial-trisomy-3q-in-a-child-with-sacrococcygeal-teratoma-and-cornelia-de-lange-syndrome-phenotype/2014-10-01T22:14:51+03:00https://www.munisdundar.com/pubs/partial-trisomy-14q-due-to-maternal-t414p16q32-in-a-dysmorphic-newborn/2014-10-01T22:16:14+03:00https://www.munisdundar.com/pubs/a-case-with-49-xxxxy-syndrome-rare-chromosomal-aneuploidies/2014-10-01T22:17:16+03:00https://www.munisdundar.com/pubs/a-study-of-cdkl5-gene-mutations-in-pediatric-patients-with-persistent-seizure-autistic-disorder-and-seizure-in-addition-to-autistic-disorder-during-infancy-and-early-childhood/2014-10-01T22:18:38+03:00https://www.munisdundar.com/pubs/progress-towards-the-golden-age-of-biotechnology/2014-10-01T22:19:23+03:00https://www.munisdundar.com/pubs/a-novel-acropectoral-syndrome-maps-to-chromosome-7q36-2/2014-11-28T22:11:40+03:00https://www.munisdundar.com/pubs/a-case-of-ambiguous-genitalia-presenting-with-a-45x46xryp11-2q11-2347xidicyp11-2idicyp11-2-karyotype-2/2014-11-28T22:41:34+03:00