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Profile

Full Name
Semerci Gündüz, Cavidan Nur
Main Affiliation
14.02. Internal Medicine
 
Email
NULL
 
Leaving Date
18-09-2017
Source ID
1005
Starting Date
26-12-2002
 
Country
Turkey
5 1 20 0 false Affiliations
End Date Organization Role Start Date
14.02. Internal Medicine Prof. Dr.
6 0 20 0 false
Status
Former staff

Publications
  • Articles
  • Others

Author

  • 5 Semerci, C.N.
  • 5 Semerci, Cavidan Nur
  • 5 Tufan, Ahmet Çevik
  • 4 Düzcan, Füsun
  • 3 Bağcı, Hüseyin
  • 3 Semerci Gündüz, Cavidan Nur
  • 3 Semerci, C.Nur
  • 2 Bagcı, Gülseren
  • 2 Bahce, M.
  • 2 Cinbiş, Mine
  • . next >

Subject

  • 16 human
  • 15 article
  • 12 Humans
  • 11 case report
  • 11 Male
  • 10 male
  • 8 Female
  • 8 female
  • 6 adult
  • 6 polymerase chain reaction
  • . next >

Date issued

  • 11 2010 - 2019
  • 11 2000 - 2009

Type

  • 22 Article

Fulltext

  • 13 No Fulltext
  • 9 With Fulltext


Results 1-20 of 22 (Search time: 0.008 seconds).

  • 1
  • 2
Issue DateTitleAuthor(s)
12006Accurate diagnosis of a Homozygous G1138A mutation in the fibroblast growth factor receptor 3 gene responsible for achondroplasiaŞatıroğlu-Tufan, Naciye Lale ; Tufan, Ahmet Çevik ; Semerci, Cavidan Nur ; Bağcı, Hüseyin 
22013Analysis of a novel AVPR2 mutation in a Turkish family with nephrogenic diabetes insipidusYaylalı, Güzin Fidan ; Bichet, D.G.; Okur, Volkan ; Levin, K.; Semerci, C. Nur 
32005Analysis of cell-free fetal DNA from maternal plasma and serum using a conventional multiplex PCR: Factors influencing successŞatiroğlu Tufan, N.L. ; Tufan, Ahmet Çevik ; Kaleli, Babür ; Yildirim, Başak ; Semerci, C. Nur ; Bağcı, Hüseyin 
42004Apert syndromeKiliç, I.; Baykara, Y.; Semerci, C.N. ; Ergin, H. ; Şatiroǧolu Tufan, N.L.
52006A case with proximal femoral focal deficiency (PFFD) and fibular A/hypoplasia (FA/H) associated with urogenital anomaliesErgin, Hacer ; Semerci, Cavidan Nur ; Bican, M.; Düzcan, Füsun ; Yagci, A.B. ; Erdogan, K.M.; Tufan, Ahmet Çevik 
62017Congenital central hypothyroidism caused by a novel thyroid-stimulating hormone-beta subunit gene mutation in two siblingsÖzhan, Bayram ; Anlaş, Ö.B.; Sarıkepe, B.; Albuz, B.; Gündüz, Nur Semerci 
72007Detection of Y chromosomal material in patients with a 45,X karyotype by PCR methodSemerci, C.N. ; Satiroglu-Tufan, N.L. ; Turan, S.; Bereket, A.; Tuysuz, B.; Yilmaz, E.; Kayserili, H.
82010The EEC syndrome and SHFM: Report of two cases and mutation analysis of p63 geneErgin, Hacer ; Semerci Gündüz, Cavidan Nur ; Tugrul Karakuş, Y. ; Scheffer, H.; Ergin, Şeniz ; Koltuksuz, U. ; Meijer, R.; Tufan, Naciye Lale 
92015Esansiyel hipertansiyonlu olgularda CHGA geni promotor bölge polimorfizmlerinin araştırılmasıEser, Metin ; Şanlıalp, Musa ; Tepeli, Emre ; Tufan, Lale Şatıroğlu ; Kaftan, Havane Asuman ; Semerci, Cavidan Nur 
102009Homozygous feature of isolated triphalangeal thumb-preaxial polydactyly linked to 7q36: No phenotypic difference between homozygotes and heterozygotesSemerci, C.N. ; Demirkan, Ahmet Fahir. ; Özdemir, Mehmet.; Biskin, E.; Akin, B.; Bagci, H.; Akarsu, N.A.
112012İdiyopatik boy kısalığı olan olgularda SHOX geni mutasyonlarının araştırılmasıÇatal, İsmail Aykut; Şatıroğlu, Lale Tufan ; Semiz, Serap ; Semerci, Nur 
122006MURCS birlikteliği ile tek taraflı over agenezisiYıldırım, Başak ; Semerci Gündüz, Cavidan Nur ; Yağcı, Ahmet Baki ; Duman, Koray; Düzcan, Füsun 
132016Mutation analysis of HSFY gene by DNA sequencing in Turkish men with idiopathic infertilitySemerci Gündüz, Cavidan Nur ; Alataş, Erkan ; Sılan, Fatma; Tufan Şatıroğlu, Naciye Lale ; Dodurga, Yavuz ; Satıroğlu, Hakan
142014Novel splice-site and missense mutations in the ALDH1A3 gene underlying autosomal recessive anophthalmia/microphthalmiaSemerci, C.N. ; Kalay, E.; Yıldırım, Cem ; Dinçer, T.; Ölmez, A.; Toraman, B.; Koçyigit, Ali 
152006Ovarian agenesis and MURCS associationYildirim, B.; Semerci, C.N. ; Ya?ci, B.; Duman, K.; Düzcan, F. 
162004Partial trisomy 18q11.2›qter due to de novo unbalanced translocation of chromosomes 15 and 18 analyzed by fluorescence in situ hybridizationSemerci, Cavidan N. ; Bahce, M.; Atik, F.; Candemir, Z.; Kiraz, I.K.; Zorlu, P.; Gül, D.
172012Patient with 45,X karyotype and severe virilization occult y sequencesÇorduk, Nergül ; Semiz, Serap ; Koltuksuz, Uğur ; Semerci, C.Nur ; Düzcan, Füsun ; Düzcan, Ender ; Şatıroğlu-Tufan, Naciye Lale
182005Prenatal diagnosis of a trisomy 13 case associated with holoprosencephaly by ultrasonography and quantitative fluorescent PCRŞatiroğlu Tufan, N. Lale ; Tufan, Ahmet Çevik ; Yildirim, B.; Kaleli, Babür ; Semerci, C.Nur ; Bir, Ferda ; Düzcan, Füsun ; Bağcı, Hüseyin 
192007Serum or plasma cartilage oligomeric matrix protein concentration as a diagnostic marker in pseudoachondroplasia: Differential diagnosis of a familyTufan, Ahmet Çevik ; Satiroglu-Tufan, Naciye Lale ; Jackson, G.C.; Semerci, Cavidan Nur ; Solak, S.; Yağcı, Baki 
202010Subtelomeric 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 syndromeSemerci, C.Nur ; Cinbiş, Mine ; Ullmann, R.; Steininger, A.; Bahce, M.; Yağcı, Baki ; Özden, Serap
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