Browsing by Author Semerci, C.N.
Showing results 1 to 5 of 5
| Issue Date | Title | Author(s) |
|---|---|---|
| 2007 | Detection of Y chromosomal material in patients with a 45,X karyotype by PCR method | Semerci, C.N.; Satiroglu-Tufan, N.L.; Turan, S.; Bereket, A.; Tuysuz, B.; Yilmaz, E.; Kayserili, H. |
| 2009 | Homozygous feature of isolated triphalangeal thumb-preaxial polydactyly linked to 7q36: No phenotypic difference between homozygotes and heterozygotes | Semerci, C.N.; Demirkan, Ahmet Fahir. ; Özdemir, Mehmet.; Biskin, E.; Akin, B.; Bagci, H.; Akarsu, N.A. |
| 2014 | Novel splice-site and missense mutations in the ALDH1A3 gene underlying autosomal recessive anophthalmia/microphthalmia | Semerci, C.N.; Kalay, E.; Yıldırım, Cem ; Dinçer, T.; Ölmez, A.; Toraman, B.; Koçyigit, Ali |
| 2004 | Obesity and genetics | Semerci, C.N. |
| 2006 | Ovarian agenesis and MURCS association | Yildirim, B.; Semerci, C.N.; Ya?ci, B.; Duman, K.; Düzcan, F. |