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X
Sırmacı, Aslı
18  Ergebnisse:
OpenAccess-Volltexte X
Personensuche X
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1

Research of genetic bases of hereditary non-syndromic heari..:

Subaşıoğlu, Aslı ; Duman, Duygu ; Sırmacı, Aslı...
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5644578/.  , 2017
Link: http://www.ncbi.nlm.nih...
 
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2

Research of genetic bases of hereditary non-syndromic heari..:

Duman, Duygu ; ERKAN, Mustafa ; SOMDAŞ, Mehmet Akif...
769a1c2b-472d-4a86-ae3a-b5de6c84a81f.  , 2017
Link: https://doi.org/10.5152/..
 
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3

Mutation of the ATP-gated P2X2 receptor leads to progressiv..:

Yan, Denise ; Zhu, Yan ; Walsh, Tom...
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3568371.  , 2013
Link: http://www.ncbi.nlm.nih...
 
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4

GPSM2 Mutations in Chudley-McCullough Syndrome:

Diaz-Horta, Oscar ; Sirmaci, Asli ; Doherty, Dan...
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3657751.  , 2012
Link: http://www.ncbi.nlm.nih...
 
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5

Mutations in OTOGL, Encoding the Inner Ear Protein Otogelin..:

Yariz, Kemal O ; Duman, Duygu ; Seco, Celia Zazo...
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3487139.  , 2012
Link: http://www.ncbi.nlm.nih...
 
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6

Mutations in CIB2, a calcium and integrin binding protein, ..:

Riazuddin, Saima ; Belyantseva, Inna A ; Giese, Arnaud...
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3501259.  , 2012
Link: http://www.ncbi.nlm.nih...
 
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7

Whole-Exome Sequencing Efficiently Detects Rare Mutations i..:

Mahdieh, Nejat ; Diaz-Horta, Oscar ; DUMAN, DUYGU...
d4fe3b16-6517-4cdd-80cd-6dd53e29ed58.  , 2012
Link: https://doi.org/10.1371/..
 
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8

Mutations in ANKRD11 Cause KBG Syndrome, Characterized by I..:

Sirmaci, Asli ; Spiliopoulos, Michail ; Brancati, Francesco...
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3155157.  , 2011
Link: http://www.ncbi.nlm.nih...
 
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9

Screening of 38 Genes Identifies Mutations in 62% of Famili..:

Duman, Duygu ; Sirmaci, Asli ; Cengiz, F. Basak..
https://aperta.ulakbim.gov.tr/record/17783.  , 2011
Link: https://aperta.ulakbim.g..
 
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10

A Truncating Mutation in SERPINB6 Is Associated with Autoso..:

Sirmaci, Asli ; Erbek, Seyra ; Price, Justin...
10.1016/j.ajhg.2010.04.004.  , 2010
Link: https://hdl.handle.net/2..
 
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11

A Truncating Mutation in SERPINB6 Is Associated with Autoso..:

Sırmacı, Aslı ; Erbek, Seyra ; Price, Justin...
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2869020.  , 2010
Link: http://www.ncbi.nlm.nih...
 
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12

A Truncating Mutation in SERPINB6 Is Associated with Autoso..:

Liu, Xue Z ; Oeztuerk, Banu ; Kulaksizoglu, Sevsen...
67362a15-2761-402b-a8a6-b9d102b8f8b5.  , 2010
Link: https://doi.org/10.1016/..
 
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13

MASP1 Mutations in Patients with Facial, Umbilical, Coccyge..:

Sirmaci, Asli ; Walsh, Tom ; Akay, Hatice...
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2978960.  , 2010
Link: http://www.ncbi.nlm.nih...
 
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14

Recurrent and Private MYO15A Mutations Are Associated with ..:

Cengiz, F. Basak ; Duman, Duygu ; Sirmaci, Asli...
https://aperta.ulakbim.gov.tr/record/25825.  , 2010
Link: https://aperta.ulakbim.g..
 
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15

Mutations in TMC1 contribute significantly to nonsyndromic ..:

Sirmaci, Asli ; Duman, Duygu ; Ozturkmen-Akay, Hatice...
https://aperta.ulakbim.gov.tr/record/40073.  , 2009
Link: https://aperta.ulakbim.g..
 
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