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Full Name
Semerci Gündüz, Cavidan Nur
Main Affiliation
Email
NULL
Leaving Date
18-09-2017
Source ID
1005
Starting Date
26-12-2002
Country
Turkey
Status
Former staff
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Results 1-20 of 22 (Search time: 0.026 seconds).
| Issue Date | Title | Author(s) | |
|---|---|---|---|
| 1 | 2006 | Accurate diagnosis of a Homozygous G1138A mutation in the fibroblast growth factor receptor 3 gene responsible for achondroplasia | Şatıroğlu-Tufan, Naciye Lale ; Tufan, Ahmet Çevik ; Semerci, Cavidan Nur ; Bağcı, Hüseyin |
| 2 | 2013 | Analysis of a novel AVPR2 mutation in a Turkish family with nephrogenic diabetes insipidus | Yaylalı, Güzin Fidan ; Bichet, D.G.; Okur, Volkan ; Levin, K.; Semerci, C. Nur |
| 3 | 2005 | Analysis of cell-free fetal DNA from maternal plasma and serum using a conventional multiplex PCR: Factors influencing success | Şatiroğlu Tufan, N.L. ; Tufan, Ahmet Çevik ; Kaleli, Babür ; Yildirim, Başak ; Semerci, C. Nur ; Bağcı, Hüseyin |
| 4 | 2004 | Apert syndrome | Kiliç, I.; Baykara, Y.; Semerci, C.N. ; Ergin, H. ; Şatiroǧolu Tufan, N.L. |
| 5 | 2006 | A case with proximal femoral focal deficiency (PFFD) and fibular A/hypoplasia (FA/H) associated with urogenital anomalies | Ergin, Hacer ; Semerci, Cavidan Nur ; Bican, M.; Düzcan, Füsun ; Yagci, A.B. ; Erdogan, K.M.; Tufan, Ahmet Çevik |
| 6 | 2017 | Congenital central hypothyroidism caused by a novel thyroid-stimulating hormone-beta subunit gene mutation in two siblings | Özhan, Bayram ; Anlaş, Ö.B.; Sarıkepe, B.; Albuz, B.; Gündüz, Nur Semerci |
| 7 | 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. |
| 8 | 2010 | The EEC syndrome and SHFM: Report of two cases and mutation analysis of p63 gene | Ergin, Hacer ; Semerci Gündüz, Cavidan Nur ; Tugrul Karakuş, Y. ; Scheffer, H.; Ergin, Şeniz ; Koltuksuz, U. ; Meijer, R.; Tufan, Naciye Lale |
| 9 | 2015 | Esansiyel hipertansiyonlu olgularda CHGA geni promotor bölge polimorfizmlerinin araştırılması | Eser, Metin ; Şanlıalp, Musa ; Tepeli, Emre ; Tufan, Lale Şatıroğlu ; Kaftan, Havane Asuman ; Semerci, Cavidan Nur |
| 10 | 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. |
| 11 | 2012 | İdiyopatik boy kısalığı olan olgularda SHOX geni mutasyonlarının araştırılması | Çatal, İsmail Aykut; Şatıroğlu, Lale Tufan ; Semiz, Serap ; Semerci, Nur |
| 12 | 2006 | MURCS birlikteliği ile tek taraflı over agenezisi | Yıldırım, Başak ; Semerci Gündüz, Cavidan Nur ; Yağcı, Ahmet Baki ; Duman, Koray; Düzcan, Füsun |
| 13 | 2016 | Mutation analysis of HSFY gene by DNA sequencing in Turkish men with idiopathic infertility | Semerci Gündüz, Cavidan Nur ; Alataş, Erkan ; Sılan, Fatma; Tufan Şatıroğlu, Naciye Lale ; Dodurga, Yavuz ; Satıroğlu, Hakan |
| 14 | 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 |
| 15 | 2006 | Ovarian agenesis and MURCS association | Yildirim, B.; Semerci, C.N. ; Ya?ci, B.; Duman, K.; Düzcan, F. |
| 16 | 2004 | Partial trisomy 18q11.2›qter due to de novo unbalanced translocation of chromosomes 15 and 18 analyzed by fluorescence in situ hybridization | Semerci, Cavidan N. ; Bahce, M.; Atik, F.; Candemir, Z.; Kiraz, I.K.; Zorlu, P.; Gül, D. |
| 17 | 2012 | Patient with 45,X karyotype and severe virilization occult y sequences | Çorduk, Nergül ; Semiz, Serap ; Koltuksuz, Uğur ; Semerci, C.Nur ; Düzcan, Füsun ; Düzcan, Ender ; Şatıroğlu-Tufan, Naciye Lale |
| 18 | 2005 | Prenatal diagnosis of a trisomy 13 case associated with holoprosencephaly by ultrasonography and quantitative fluorescent PCR | Şatiroğlu Tufan, N. Lale ; Tufan, Ahmet Çevik ; Yildirim, B.; Kaleli, Babür ; Semerci, C.Nur ; Bir, Ferda ; Düzcan, Füsun ; Bağcı, Hüseyin |
| 19 | 2007 | Serum or plasma cartilage oligomeric matrix protein concentration as a diagnostic marker in pseudoachondroplasia: Differential diagnosis of a family | Tufan, Ahmet Çevik ; Satiroglu-Tufan, Naciye Lale ; Jackson, G.C.; Semerci, Cavidan Nur ; Solak, S.; Yağcı, Baki |
| 20 | 2010 | 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 | Semerci, C.Nur ; Cinbiş, Mine ; Ullmann, R.; Steininger, A.; Bahce, M.; Yağcı, Baki ; Özden, Serap |