CLINICAL AND MOLECULAR RESULTS OF SIX CASES WITH ROBERTS SYNDROME: REVIEW OF CASES FROM TURKIYE

CLINICAL AND MOLECULAR RESULTS OF SIX CASES WITH ROBERTS SYNDROME: REVIEW OF CASES FROM TURKIYE

Objective: Roberts syndrome is a rare autosomal recessive disease characterized by limb defects, prenatal onset growth retardation, and craniofacial anomalies. We aimed to compare the clinical and molecular findings of six cases with Roberts syndrome with the previously reported patients from Turkiy...

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Bibliographic Details
Main Authors: Ayça Dilruba Aslanger, Tuğba Kalaycı, Esma Nur Konur, Çağrı Güleç, Şahin Avcı, Umut Altunoğlu, Volkan Karaman, Güven Toksoy, Birsen Karaman, Seher Başaran, Zehra Oya Uyguner, Gözde Yeşil Sayın
Format: Article
Language:English
Published: Istanbul University Press 2022-10-01
Series:İstanbul Tıp Fakültesi Dergisi
Subjects:
roberts syndrome
esco2
tetraphocomelia
Online Access:https://cdn.istanbul.edu.tr/file/JTA6CLJ8T5/4DF4C08F634E46B48D3A6B8D19AECBFC
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https://cdn.istanbul.edu.tr/file/JTA6CLJ8T5/4DF4C08F634E46B48D3A6B8D19AECBFC

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