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Tuncez, Ebru
22  results:
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1

Assessment of Pathogenic Variants in the PAH Gene and Genot..:

Balasar, Özgür ; Kadıoğlu Yılmaz, Banu ; Başdemirci, Müşerref...
Biochemical Genetics.  , 2024
Link: https://doi.org/10.1007/..
 
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2

High diagnostic yield with algorithmic molecular approach o..:

Ceylan, Gülay Güleç ; Habiloğlu, Esra ; Çavdarlı, Büşranur...
Revista da Associação Médica Brasileira.  69 (2023)  2 - p. 233-239 , 2023
Link: https://doi.org/10.1590/..
 
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3

MYSTERY OF iAMP:

KURTİPEK, Fatma Burçin ; KAÇAR, Dilek ; TUNÇEZ, Ebru..
Hematology, Transfusion and Cell Therapy.  43 (2021)  - p. S25-S26 , 2021
Link: https://doi.org/10.1016/..
 
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4

Response to Letter to the Editor: "Atrioventricular canal d..:

Gumus, Evren ; Tuncez, Ebru ; Oz, Ozlem.
Annals of Human Genetics.  85 (2021)  3-4 - p. 103-104 , 2021
Link: https://doi.org/10.1111/..
 
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5

Clinical and exome sequencing findings in seven children wi..:

Gumus, Evren ; Tuncez, Ebru ; Oz, Ozlem.
Annals of Human Genetics.  85 (2020)  1 - p. 27-36 , 2020
Link: https://doi.org/10.1111/..
 
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6

Peutz-Jeghers Syndrome: A Very Rare Cause of Iron Deficienc..:

Demir Yenigürbüz, Fatma ; Deveci, Uğur ; Tuncez, Ebru
Turkish Journal of Hematology.  36 (2019)  1 - p. 50-51 , 2019
Link: https://doi.org/10.4274/..
 
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7

Peutz–Jeghers syndrome:A very rare cause of iron deficiency..:

Demir Yenigürbüz, Fatma ; Deveci, Uğur ; Tuncez, Ebru
Turkish Journal of Hematology.  , 2018
Link: https://doi.org/10.4274/..
 
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8

Chanarin-Dorfman syndrome: A case report:

Mungan, Neslihan Onenli ; Tuncez, Ebru ; Yilmaz, Berna Seker...
Molecular Genetics and Metabolism.  117 (2016)  2 - p. S87-S88 , 2016
Link: https://doi.org/10.1016/..
 
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9

Recurrent proximal 18p monosomy and 18q trisomy in a family..:

Zamani, Ayse Gul ; Acar, Aynur ; Durakbasi‐Dursun, Gul...
American Journal of Medical Genetics Part A.  164 (2014)  5 - p. 1239-1244 , 2014
Link: https://doi.org/10.1002/..
 
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10

Micronuclei frequencies in lymphocytes and cervical cells o..:

Zamani, Ayşe Gül ; Gezginç, Kazım ; Yıldırım, Mahmut Selman...
Turkish Journal of Obstetrics and Gynecology.  , 2017
Link: https://hdl.handle.net/2..
 
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11

Are angiotensin converting enzyme (ACE1/ACE2) gene variants..:

Serdal Baştuğ ; Büşranur Çavdarlı ; Aliye Baştuğ...
https://jag.journalagent.com/z4/download_fulltext.asp?pdir=anatoljcardiol&un=AJC-21624.  , 2022
Link: https://doi.org/10.5152/..
 
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12

Are angiotensin converting enzyme (ACE1/ACE2) gene variants..:

Serdal Baştuğ ; Büşranur Çavdarlı ; Aliye Baştuğ...
https://anatoljcardiol.com/jvi.aspx?un=AJC-21624&volume=26&issue=2.  , 2022
Link: https://doi.org/10.5152/..
 
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13

MYSTERY OF iAMP:

Fatma Burçin KURTİPEK ; Dilek KAÇAR ; Ebru TUNÇEZ..
http://www.sciencedirect.com/science/article/pii/S253113792101141X.  , 2021
Link: https://doi.org/10.1016/..
 
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14

Beta-thalassemia mutation types and the relationship with t..:

Ebru Tuncez ; Özlem Öz ; Burcu Akıncı.
https://dergipark.org.tr/en/download/article-file/1327750.  , 2021
Link: https://doi.org/10.22391..
 
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15

Peutz-Jeghers Syndrome: A Very Rare Cause of Iron Deficienc..:

Fatma Demir Yenigürbüz ; Uğur Deveci ; Ebru Tuncez
https://jag.journalagent.com/z4/download_fulltext.asp?pdir=tjh&un=TJH-39215.  , 2019
Link: https://doi.org/10.4274/..
 
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