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Ergin, Filiz Başak Cengiz
7  results:
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1

A Turkish case of incontinentia pigmenti with a deletion mu..:

Ergin, Filiz Başak Cengiz ; Tekin, Mustafa ; Güneş, Meltem...
Egyptian Journal of Medical Human Genetics.  23 (2022)  1 - p. , 2022
Link: https://doi.org/10.1186/..
 
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2

Hypophosphatasia: is it an underdiagnosed disease even by e..:

İnci, Aslı ; Ergin, Filiz Başak Cengiz ; Yüce, Burcu Topcu...
Journal of Bone and Mineral Metabolism.  39 (2021)  4 - p. 598-605 , 2021
Link: https://doi.org/10.1007/..
 
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3

A possibly new autoinflammatory disease due to compound het..:

Yıldız, Çisem ; Gezgin Yıldırım, Deniz ; Inci, Asli...
Joint Bone Spine.  90 (2023)  1 - p. 105490 , 2023
Link: https://doi.org/10.1016/..
 
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4

The first case with FBXL4 mutation successfully treated wit..:

İnci, Aslı ; Aktaş, Emine ; Cengiz Ergin, Filiz Başak...
Journal of Parenteral and Enteral Nutrition.  45 (2021)  8 - p. 1788-1792 , 2021
Link: https://doi.org/10.1002/..
 
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5

A Turkish case of incontinentia pigmenti with a deletion mu..:

Filiz Başak Cengiz Ergin ; Mustafa Tekin ; Meltem Güneş...
https://doi.org/10.1186/s43042-022-00215-x.  , 2022
Link: https://doi.org/10.1186/..
 
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6

Familial neonatal Marfan syndrome due to parental mosaicism..:

Tekin, Mustafa ; Cengiz, Filiz Başak ; Ayberkin, Eda...
American Journal of Medical Genetics Part A.  143A (2007)  8 - p. 875-880 , 2007
Link: https://doi.org/10.1002/..
 
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7

Bloodstream infections due to Trichosporon species in paedi..:

Akaslan Kara, Aybüke ; Çay, Ümmühan ; Yalçınkaya, Rumeysa...
Journal of Medical Mycology.  32 (2022)  1 - p. 101229 , 2022
Link: https://doi.org/10.1016/..
 
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