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| dc.contributor.author | ERÇAL, MURAT DERYA
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| dc.contributor.author | BORA, ELÇİN
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| dc.contributor.author | ÜLGENALP, AYFER
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| dc.contributor.author | Paytoncu, Şebnem
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| dc.contributor.author | ÜNAL, NURETTİN
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| dc.contributor.author | GİRAY BOZKAYA, ÖZLEM
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| dc.date.accessioned | 2015-10-08T15:16:40Z | NULL |
| dc.date.available | 2015-10-08T15:16:40Z | NULL |
| dc.date.issued | 2007 | |
| dc.identifier.uri | http://hdl.handle.net/20.500.12397/2942 | NULL |
| dc.description.abstract | Watson sendromu, café-au-lait lekeleri, pulmoner stenoz, mental retardasyon, boy kısalığıile karakterizedir. Bu makalede, moleküler temeli henüz tartışmalı olan ve seyrek görülen bubirlikteliği hatırlatmak amacıyla Watson sendromlu 13 yaşında bir kız olgu sunuldu.Watson syndrome is characterized by café-au-lait spots, pulmonary valvular stenosis,mental retardation and short stature. In this report, we present a thirteen-year-old girl withWatson syndrome to remind this disease which is seldom encountered and the molecularbasis is still controversial. | en_US |
| dc.language.iso | tr | en_US |
| dc.publisher | Dokuz Eylül Üniversitesi Tıp Fakültesi | en_US |
| dc.subject | Watson sendromu, nörofibromatozis, pulmoner stenoz, café-au-laitlekesiWatson syndrome, neurofibromatosis, pulmoner stenosis, café-au-lait spot | en_US |
| dc.title | Watson Sendromu | en_US |
| dc.title.alternative | WATSON SYNDROME | en_US |
| dc.type | Article | en_US |
