Tuncbilek, Ergul: search on Z-Library

The world's largest scientific articles store. 70,000,000+ articles for free.

Don't use scam websites

1

Congenital contractural arachnodactyly (Beals syndrome)

Ergül Tunçbilek, Yasemin Alanay

Journal:

Orphanet Journal of Rare Diseases

Year:

2006

Language:

english

File:

PDF, 131 KB

english, 2006

2

Prevalence of Allergic Diseases and Influencing Factors in Primary-School Children in the Ankara Region of Turkey

Saraçlar, Yildiz, Yiĝit, Sule, Adalioĝlu, Gönül, Tuncer, Ayfer, Tunçbilek, Ergül

Journal:

Journal of Asthma

Year:

1997

Language:

english

File:

PDF, 543 KB

english, 1997

3

Fragile x-associated premature ovarian failure in a large Turkish cohort: Findings of Hacettepe Fragile X Registry

Utine, Gülen Eda, Şimşek-Kiper, Pelin Özlem, Akgün-Doğan, Özlem, Ürel-Demir, Gizem, Alanay, Yasemin, Aktaş, Dilek, Boduroğlu, Koray, Tunçbilek, Ergül, Alikaşifoğlu, Mehmet

Journal:

European Journal of Obstetrics & Gynecology and Reproductive Biology

Year:

2018

Language:

english

File:

PDF, 472 KB

english, 2018

4

Loss of maternal allele in a child with myelodysplastic syndrome and monosomy 7

Aktas, Dilek, Yenicesu, Id?l, H?csonmez, Gonul, Tuncbilek, Ergul

Journal:

American Journal of Hematology

Year:

1999

Language:

english

File:

PDF, 72 KB

english, 1999

5

Screening for the fragile X syndrome among mentally retarded males by hair root analysis

Ergül Tunçbilek, Mehmet Alikasifoğlu, Dilek Aktas, Funda Duman, Hulya Yanik, Burçu Anar, Ben Oostra, Rob Willemsen

Journal:

American Journal of Medical Genetics Part A

Year:

2000

Language:

english

File:

PDF, 1.29 MB

english, 2000

6

Methylenetetrahydrofolate reductase enzyme polymorphisms as maternal risk for down syndrome among Turkish women

Koray Boduroğlu, Yasemin Alanay, Berrin Koldan, Ergül Tunçbilek

Journal:

American Journal of Medical Genetics Part A

Year:

2004

Language:

english

File:

PDF, 78 KB

english, 2004

7

Response to the letter to “MTHTR 677C-T polymorphism is not excluded as maternal risk for Down syndrome among Turkish women”

Koray Boduroğlu, Yasemin Alanay, Berrin Koldan, Ergül Tunçbilek

Journal:

American Journal of Medical Genetics Part A

Year:

2005

Language:

english

File:

PDF, 31 KB

english, 2005

8

Is Dandy–Walker malformation associated with “distal 13q deletion syndrome”? Findings in a fetus supporting previous observations

Yasemin Alanay, Dilek Aktaş, Eda Utine, Beril Talim, Lütfü Önderoğlu, Melda Çağlar, Ergül Tunçbilek

Journal:

American Journal of Medical Genetics Part A

Year:

2005

Language:

english

File:

PDF, 139 KB

english, 2005

9

Spondylo-ocular syndrome: A new entity involving the eye and spine

Yasemin Alanay, Andrea Superti-Furga, Fatih Karel, Ergül Tunçbilek

Journal:

American Journal of Medical Genetics Part A

Year:

2006

Language:

english

File:

PDF, 194 KB

english, 2006

10

Frontometaphyseal dysplasia: A case with Arnold–Chiari malformation and bracket epiphysis of the first metacarpal bone

Koray Boduroglu, Ergül Tuncbilek

Journal:

Pediatrics International

Year:

1999

Language:

english

File:

PDF, 82 KB

english, 1999

11

Derivative chromosome 1 andGLUT1deficiency syndrome in a sibling pair

Dilek Aktas, Eda G Utine, Kristin Mrasek, Anja Weise, Ferdinand von Eggeling, Kalbiye Yalaz, Nicole Posorski, Nurten Akarsu, Mehmet Alikasifoglu, Thomas Liehr, Ergul Tuncbilek

Journal:

Molecular Cytogenetics

Year:

2010

Language:

english

File:

PDF, 2.27 MB

english, 2010

12

Clinically abnormal case with paternally derived partial trisomy 8p23.3 to 8p12 including maternal isodisomy of 8p23.3: a case report

Dilek Aktas, Anja Weise, Eda Utine, Dursun Alehan, Kristin Mrasek, Ferdinand von Eggeling, Heike Thieme, Ergul Tuncbilek, Thomas Liehr

Journal:

Molecular Cytogenetics

Year:

2009

Language:

english

File:

PDF, 575 KB

english, 2009

13

Hereditary congenital coxa vara with dominant inheritance?

Burhan Say, Ergül Tunçbilek, Tuĝrul Pirnar, Nejat Tokgözoglu

Journal:

Year:

1971

Language:

english

File:

PDF, 166 KB

english, 1971

14

45,XO Turner's syndrome, Wilm's tumor and imperforate anus

Burhan Say, Sevim Balci, Ergül Tunçbilek

Journal:

Year:

1971

Language:

english

File:

PDF, 162 KB

english, 1971

15

A familial syndrome of unusual facies associated with malocclusion and short stature

Burhan Say, Ergul Tuncbilek, Tugrul Pirnar

Journal:

Year:

1973

Language:

english

File:

PDF, 213 KB

english, 1973

16

Trisomy-8 syndrome

Ergül Tuncbilek, Charlotte Halicioglu, Burhan Say

Journal:

Year:

1974

Language:

english

File:

PDF, 390 KB

english, 1974

17

Giemsa banding in the D1trisomy syndrome

Charlotte Boone Halicioglu, Ergül Tuncbilek, Burhan Say

Journal:

Year:

1972

Language:

english

File:

PDF, 102 KB

english, 1972

18

Terminal phalangeal accessory ossification center of the thumb: an additional radiographic finding in Larsen syndrome

Yasemin Alanay, Gulen Eda Utine, Ralph S. Lachman, Deborah Krakow, Ergul Tuncbilek

Journal:

Pediatric Radiology

Year:

2006

Language:

english

File:

PDF, 169 KB

english, 2006

19

Analysis of 65 Turkish patients with congenital aplastic anemia (Fanconi anemia and non-Fanconi anemia): Hacettepe experience

Çiǧjdem Altay, Mehmet Alikaşifoǧlu, Abdurrahman Kara, Ergül Tunçbilek, Namik Özbek, Trautte M. Schroeder-Kurth

Journal:

Clinical Genetics

Year:

1997

Language:

english

File:

PDF, 1.27 MB

english, 1997

20

CYP1A1 Gene Polymorphism and Risk of Epithelial Ovarian Neoplasm

Dilek Aktas, Inci Guney, Mehmet Alikasifoglu, Kunter Yüce, Ergul Tuncbilek, Ali Ayhan

Journal:

Gynecologic Oncology

Year:

2002

Language:

english

File:

PDF, 40 KB

english, 2002

21

High frequency hearing loss in Ullrich-Turner syndrome

Güngör, Neslihan, Böke, Bilgehan, Belgin, Erol, Tunçbilek, Ergül

Journal:

European Journal of Pediatrics

Year:

2000

Language:

english

File:

PDF, 108 KB

english, 2000

22

Mutations in the Gene Encoding the RER Protein FKBP65 Cause Autosomal-Recessive Osteogenesis Imperfecta

Yasemin Alanay, Hrispima Avaygan, Natalia Camacho, G. Eda Utine, Koray Boduroglu, Dilek Aktas, Mehmet Alikasifoglu, Ergul Tuncbilek, Diclehan Orhan, Filiz Tiker Bakar, Bernard Zabel, Andrea Superti-Fu

Journal:

The American Journal of Human Genetics

Year:

2010

Language:

english

File:

PDF, 1.28 MB

english, 2010

23

Mutations in the Gene Encoding the RER Protein FKBP65 Cause Autosomal-Recessive Osteogenesis Imperfecta

Yasemin Alanay, Hrispima Avaygan, Natalia Camacho, G. Eda Utine, Koray Boduroglu, Dilek Aktas, Mehmet Alikasifoglu, Ergul Tuncbilek, Diclehan Orhan, Filiz Tiker Bakar, Bernard Zabel, Andrea Superti-Fu

Journal:

The American Journal of Human Genetics

Year:

2010

Language:

english

File:

PDF, 232 KB

english, 2010

24

CYP1A1 and GSTM1 polymorphic genotypes in patients with prostate cancer in a Turkish population

Dilek Aktas, Metin Hascicek, Sinan Sozen, Haluk Ozen, Ergul Tuncbilek

Journal:

Cancer Genetics and Cytogenetics

Year:

2004

Language:

english

File:

PDF, 166 KB

english, 2004

25

Myelodysplastic syndrome associated with monosomy 7 in childhood: a retrospective study

Dilek Aktas, Ergul Tuncbilek

Journal:

Cancer Genetics and Cytogenetics

Year:

2006

Language:

english

File:

PDF, 86 KB

english, 2006

26

CYP1A1 gene polymorphism as a risk factor for cervical intraepithelial neoplasia and invasive cervical cancer

Cagatay Taskiran, Dilek Aktas, Nilufer Yigit-Celik, Mehmet Alikasifoglu, Kunter Yuce, Ergül Tunçbilek, Ali Ayhan

Journal:

Gynecologic Oncology

Year:

2006

Language:

english

File:

PDF, 91 KB

english, 2006

27

A comparison of the effect of high-dose methylprednisolone with conventional-dose prednisolone in acute lymphoblastic leukemia patients with randomization

Sevgi Yetgin, Aytemiz Gürgey, A Murat Tuncer, Mualla Çetin, Namik Özbek, Tülin Şayli, Ertuğrul Güler, Abdurrahman Kara, Lale Olcay, Feride Duru, Fatma Gümrük, Lale Atahan, Ergul Tunçbilek

Journal:

Leukemia Research

Year:

1998

Language:

english

File:

PDF, 179 KB

english, 1998

28

Glutathione S-transferase M1 gene polymorphism in bladder cancer patients: a marker for invasive bladder cancer?

Dilek Aktas, Haluk Ozen, Necmettin Atsu, Ali Tekin, Sinan Sozen, Ergul Tuncbilek

Journal:

Cancer Genetics and Cytogenetics

Year:

2001

Language:

english

File:

PDF, 52 KB

english, 2001

29

Tetrasomy 8 as a primary chromosomal abnormality in a child with acute megakaryoblastic leukemia: a case report and review of the literature

Dilek Aktas, Ergul Tuncbilek, Mualla Cetin, Gonul Hicsonmez

Journal:

Cancer Genetics and Cytogenetics

Year:

2001

Language:

english

File:

PDF, 555 KB

english, 2001

30

Myelodysplastic Syndrome Associated with Monosomy 7 in a Child with Bloom Syndrome

Dilek Aktas, Ahmet Koc, Koray Boduroglu, Gonul Hicsonmez, Ergul Tuncbilek

Journal:

Cancer Genetics and Cytogenetics

Year:

2000

Language:

english

File:

PDF, 947 KB

english, 2000

31

Ipsilateral foot and controlateral hand anomalies in a patient with Poland–Moebius syndrome

İbrahim İlker Çetin, Dilek Aktaş, Ergül Tunçbilek

Journal:

European Journal of Medical Genetics

Year:

2005

Language:

english

File:

PDF, 174 KB

english, 2005

32

Central precocious puberty in a girl with Williams syndrome: the result of treatment with GnRH analogue

G. Eda Utine, Ayfer Alikasifoglu, Mehmet Alikasifoglu, Ergul Tuncbilek

Journal:

European Journal of Medical Genetics

Year:

2006

Language:

english

File:

PDF, 132 KB

english, 2006

33

Isodicentric Y (p11.32) chromosome in an infant with mixed gonadal dysgenesis

Dilek Aktas, Mehmet Alikasifoglu, Nazlı Gonc, Mehmet E. Senocak, Ergul Tuncbilek

Journal:

European Journal of Medical Genetics

Year:

2006

Language:

english

File:

PDF, 271 KB

english, 2006

34

Cryptic trisomy 5q35.2qter and deletion 1p36.3 characterised using FISH and array-based CGH

Eda G. Utine, Yasemin Alanay, Dilek Aktas, Mehmet Alikasifoglu, Koray Boduroglu, Joris Vermeesch, Ergul Tuncbilek, Jean-Pierre Fryns

Journal:

European Journal of Medical Genetics

Year:

2008

Language:

english

File:

PDF, 489 KB

english, 2008

35

A Hypotonic Infant With Tachycardia and Fever of Unknown Origin

S. Songül Yalçın, Eren Kale, Haluk Topaloğlu, Ergül Tunçbilek

Journal:

Journal of Pediatric Health Care

Year:

2007

Language:

english

File:

PDF, 98 KB

english, 2007

36

Implications of certain genetic polymorphisms in scarring in vesicoureteric reflux: Importance of ace polymorphism

Seza Ozen, Mehmet Alikasifoglu, Umit Saatci, Aysin Bakkaloglu, Nesrin Besbas, Nazli Kara, Hulusi Kocak, Belkis Erbas, Ibrahim Unsal, Ergul Tuncbilek

Journal:

American Journal of Kidney Diseases

Year:

1999

Language:

english

File:

PDF, 39 KB

english, 1999

37

A Hypotonic Infant With Tachycardia and Fever of Unknown Origin

S. Songül Yalçın, Eren Kale, Haluk Topaloğlu, Ergül Tunçbilek

Journal:

Journal of Pediatric Health Care

Year:

2007

Language:

english

File:

PDF, 45 KB

english, 2007

38

CYP1A1 gene polymorphism and polycystic ovary syndrome

Ibrahim Esinler, Dilek Aktas, Umit Otegen, Mehmet Alikasifoglu, Hakan Yarali, Ergul Tuncbileke

Journal:

Reproductive BioMedicine Online

Year:

2008

Language:

english

File:

PDF, 160 KB

english, 2008

39

45, XO/46, XYq dic mosaicism in a patient with ambiguous genitalia

Ergul Tuncbilek, Charlotte Halicioglu, Martin Bobrow, Kemal Ustay

Journal:

Clinical Genetics

Year:

1976

Language:

english

File:

PDF, 402 KB

english, 1976

40

Aglossia-adactylia syndrome (special emphasis on the inheritance pattern)

Ergul Tuncbilek, Cengiz Yalcin, Metin Atasu

Journal:

Clinical Genetics

Year:

1977

Language:

english

File:

PDF, 254 KB

english, 1977

41

Bilateral Poland anomaly

İbrahim Karnak, F. Cahit Tanyel, Ergül Tunçbilek, Metin Ünsal, Nebil Büyükpamukçu

Journal:

American Journal of Medical Genetics

Year:

1998

Language:

english

File:

PDF, 122 KB

english, 1998

42

DERMATOGLYPHIC FINDINGS IN LAURENCE-MOON-BIEDL SYNDROME

Atasu, Metin, Balci, Sevim, Tuncbilek, Ergul, Say, Burhan

Journal:

Year:

1973

Language:

english

File:

PDF, 252 KB

english, 1973

43

LACTOSE INTOLERANCE IN TURKEY

Tuncbilek, Ergül, Türün, Rikkat, Say, Burhan

Journal:

Year:

1973

Language:

english

File:

PDF, 157 KB

english, 1973

44

DERMATOGLYPHICS IN TRISOMY 8

Tuncbilek, Ergül, Atasu, Metin, Say, Burhan

Journal:

Year:

1972

Language:

english

File:

PDF, 140 KB

english, 1972

45

Methylene tetrahydrofolate reductase polymorphisms and homocysteine level in heart defects

Sahiner, Umit M, Alanay, Yasemin, Alehan, Dursun, Tuncbilek, Ergul, Alikasifoglu, Mehmet

Journal:

Pediatrics International

Year:

2014

Language:

english

File:

PDF, 102 KB

english, 2014

46

Tetraploid/Diploid Mosaicism With Generalized Aggressive Periodontitis

Tözüm, Tolga F., Berker, Ezel, Akincibay, Hakan, Özer, Özlem, Aktaş, Dilek, Tezcan, Ilhan, Şekerci, Sükran Ç., El, Hakan, Eratalay, Kenan, Tunçbilek, Ergül

Journal:

Journal of Periodontology

Year:

2005

Language:

english

File:

PDF, 196 KB

english, 2005

47

Evaluation of Children with Myelodysplastic Syndrome: Importance of Extramedullary Disease as a Presenting Symptom

Hiçsönmez, Gönül, Çetin, Mualla, Yenicesu, Idil, Olcay, Lale, Koç, Ahmet, Aktas, Dilek, Tunçbilek, Ergül, Tuncer, Murat

Journal:

Leukemia and Lymphoma

Year:

2001

Language:

english

File:

PDF, 766 KB

english, 2001

48

Chromosomal Mosaicism in a Pregnant Woman Treated with Acyclovir for Herpes Simplex Encephalitis

Aktas, Dilek, Tuncbilek, Ergul, Onderoglu, Lutfi

Journal:

American Journal of Perinatology

Year:

2001

Language:

english

File:

PDF, 457 KB

english, 2001

49

Cavernous malformation with Poland–Möbius syndrome

Mut, Melike, Palaoglu, Selcuk, Alanay, Yasemin, Ismailoglu, Ozgur, Tuncbilek, Ergul

Journal:

Journal of Neurosurgery Pediatrics

Year:

2007

Language:

english

File:

PDF, 230 KB

english, 2007

50

Acute Lymphoblastic Leukemia Associated with Klinefelter Syndrome

Gürgey, Aytemiz, Kara, Abdurrahman, Tuncer, Murat, Alikasifoglu, Mehmet, Tunçbilek, Ergül

Journal:

Pediatric Hematology-Oncology

Year:

1994

Language:

english

File:

PDF, 266 KB

english, 1994