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Journal of Pediatric and Adolescent Gynecology|July 16, 2014
Frequency and types of chromosomal abnormalities in Turkish women with amenorrheaOsman Demirhan, Nilgün Tanrıverdi, Erdal Tunç, et al.
Asian Pacific Journal of Cancer Prevention : APJCP|January 16, 2013
Chromosome imbalances and alterations of AURKA and MYCN genes in children with neuroblastomaNihal Inandiklioğlu, Sema Yilmaz, Osman Demirhan, et al.
Reproductive Biomedicine Online|February 15, 2016
Chromosomal analyses of 1510 couples who have experienced recurrent spontaneous abortionsErdal Tunç, Nilgün Tanrıverdi, Osman Demirhan, et al.
Indian Journal of Human Genetics|November 18, 2011
The first report described as an important study: The association of mannose-binding lectin gene 2 polymorphisms in children with Down syndromeOsman Demirhan, Deniz Taştemir, Ramazan Güneşaçar, et al.
Tuberkuloz Ve Toraks|May 11, 2011
Polymorphisms in NRAMP1 and MBL2 genes and their relations with tuberculosis in Turkish childrenHüseyin Avni Solğun, Deniz Taştemir, Necmi Aksaray, et al.
Yonsei Medical Journal|September 2, 2003
A cytogenetic study in 120 Turkish children with intellectual disability and characteristics of fragile X syndromeOsman Demirhan, Deniz Taştemir, Rasim Somer Diler, et al.
Saudi Medical Journal|July 16, 2008
Correlation of clinical phenotype with a pericentric inversion of chromosome 9 and genetic counselingOsman Demirhan, Ayfer Pazarbasi, Dilara Suleymanova-Karahan, et al.
Ecotoxicology and Environmental Safety|March 28, 2016
Effects of GSM-like radiofrequency irradiation during the oogenesis and spermiogenesis of Xenopus laevisAyper Boga, Mustafa Emre, Yasar Sertdemir, et al.
European Journal of Human Genetics : EJHG|March 28, 2008
Cerebellar hypoplasia, with quadrupedal locomotion, caused by mutations in the very low-density lipoprotein receptor geneS Türkmen, K Hoffmann, Osman Demirhan, et al.
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