dc.contributor.author |
Demiral, Emine |
|
dc.contributor.author |
Sen, Askin |
|
dc.contributor.author |
Esener, Zeynep |
|
dc.contributor.author |
Ceylaner, Serdar |
|
dc.contributor.author |
Tekedereli, Ibrahim |
|
dc.date.accessioned |
2019-07-04T07:16:12Z |
|
dc.date.available |
2019-07-04T07:16:12Z |
|
dc.date.issued |
2018 |
|
dc.identifier.citation |
Demiral, E. Sen, A. Esener, Z. Ceylaner, S. Tekedereli, Iç (2018). A rare mutation in the epg5 gene causes vici syndrome. Cilt:27. Sayı:4.145-147 ss. |
tr_TR |
dc.identifier.uri |
http://hdl.handle.net/11616/12313 |
|
dc.language.iso |
eng |
tr_TR |
dc.publisher |
Lıppıncott wıllıams & wılkıns, two commerce sq, 2001 market st, phıladelphıa, pa 19103 usa |
tr_TR |
dc.relation.isversionof |
A rare mutation in the epg5 gene causes vici syndrome |
tr_TR |
dc.rights |
info:eu-repo/semantics/openAccess |
tr_TR |
dc.subject |
Sensorıneural hearıng-loss |
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dc.subject |
corpus-callosum |
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dc.subject |
muscle bıopsy |
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dc.subject |
ımmunodefıcıency |
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dc.subject |
hypopıgmentatıon |
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dc.subject |
agenesıs |
tr_TR |
dc.title |
A rare mutation in the epg5 gene causes vici syndrome |
tr_TR |
dc.type |
article |
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dc.relation.journal |
Clınıcal dysmorphology |
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dc.contributor.department |
İnönü Üniversitesi |
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dc.identifier.volume |
27 |
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dc.identifier.issue |
4 |
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dc.identifier.startpage |
145 |
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dc.identifier.endpage |
147 |
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