Medical Genetics is the official publication of the Turkish Society of Medical Genetics. It is electronically published three times a year (January, May, September).
Medical Genetics is an open access, peer-reviewed journal that considers articles on the effects of genetics and heredity in individuals, families and among populations in relation to human health and disease. The journal welcomes manuscripts in English and Turkish, and publishes original research papers, editorials, review articles, case reports, short reports, letters to the editor, the scientific correspondence and announcements relevant to the development of research, education and medical application in the field of human genetics nationwide and all over the world. Our main areas of interests are monogenic and multifactorial disorders, epigenetics and non-mendelian conditions, development and malformation, human genomics and proteomics, cancer genetics, gene mapping and functional studies, genotype-phenotype correlations, diagnostics, prenatal diagnosis, therapy and prevention, animal models, genetic services, community genetics, personalized medicine, genetic variation and genome diversity in Turkey and other areas of the World.
The journal will also publish invited editorials and commentaries, announcements of Societal and other Turkish activities and special issues of general interest for the Turkish Medical Genetics community.
All editorial correspondence should be sent to:
Medical Genetics Journal
Department of Medical Genetics
University of Istanbul, Cerrahpasa Medical Faculty
Phone: +90 212 414 30 00/ext.22658
Fax: +90 212 414 31 84
Sayfalar 1 - 2 Hakan Ulucan
Sayfalar 3 - 5 Hakan Ulucan
Research of interchromosomal effect in male carriers with chromosomal heteromorphism by using FISH
Sayfalar 1 - 8 Özgür Balasar, Hasan Acar
Türkiye'deki bir ailede heterozigot p63 mutasyonunun neden olduğu Hay Wells
Sayfalar 18 - 21 Esra Ataman, Sukru Candan, Margherita Silengo
45,X/47,XXX ve beş gebelik: Beşte bir başarı
Sayfalar 22 - 24 Hatice Koçak Eker
Romano-Ward sendromunda KCNQ1 geninde bir duplikasyon mutasyonu
Sayfalar 25 - 28 Salih Coskun, Yasar Yildirim, Abdullah Cim, Yahya Islamoglu, Umut Altunoglu, Z Oya Uyguner, Osman Gokalp
Rejecting paternity with X STR anlysis: a case report
Sayfalar 29 - 32 Ramazan Emre, Kemal Cantürk, Bünyamin Başpınar, Muhammed Doğan, İlhami Kömür, Ömer Müslümanoğlu
Sayfalar 33 - 35 Ayşe Gül Zamani, M. Selman YILDIRIM, Nazım Karalezli