Derbent, Murat
32  results:
Search for persons X
?
 
?
2

Mutations in LONP1, a mitochondrial matrix protease, cause ..:

Dikoglu, Esra ; Alfaiz, Ali ; Gorna, Maria...
American Journal of Medical Genetics Part A.  167 (2015)  7 - p. 1501-1509 , 2015
 
?
4

A patient with Keipert syndrome and isolated fibrous dyspla..:

Derbent, Murat ; Bıkmaz, Yunus Emre ; Agildere, Muhtesem
American Journal of Medical Genetics Part A.  155 (2011)  6 - p. 1496-1499 , 2011
 
?
5

Clinical and hematologic findings in Noonan syndrome patien..:

Derbent, Murat ; Oncel, Yekta ; Tokel, Kürşad...
American Journal of Medical Genetics Part A.  152A (2010)  11 - p. 2768-2774 , 2010
 
?
 
?
9

PHACES syndrome with small, late-onset hemangiomas:

Torer, Bırgın ; Gulcan, Hande ; Kilicdag, Hasan.
European Journal of Pediatrics.  166 (2007)  12 - p. 1293-1295 , 2007
 
?
10

Congenital partial arhinia: a case report:

Akkuzu, Guzin ; Akkuzu, Babur ; Aydin, Erdinc..
Journal of Medical Case Reports.  1 (2007)  1 - p. , 2007
 
?
11

Variable phenotype and associations in chromosome 22q11.2 m..:

Derbent, Murat ; Bikmaz, Yunus Emre ; Yilmaz, Zerrin.
American Journal of Medical Genetics Part A.  140A (2006)  6 - p. 659-660 , 2006
 
?
12

Two neurofibromatosis type 1 cases associated with rhabdomy..:

Oguzkan, Sibel ; Terzi, Yunus Kasım ; Güler, Elif...
Cancer Genetics and Cytogenetics.  164 (2006)  2 - p. 159-163 , 2006
 
?
14

Congenital cataract, microphthalmia, hypoplasia of corpus c..:

Derbent, Murat ; Agras, Pinar Isık ; Gedik, Şansal...
American Journal of Medical Genetics Part A.  128A (2004)  3 - p. 232-234 , 2004
 
?
15

Dysplastic changes in the peripheral blood of children with..:

Özbek, Namık ; Derbent, Murat ; Olcay, Lale..
American Journal of Hematology.  77 (2004)  2 - p. 126-131 , 2004
 
1-15