Multipl konjenital anomalilerin eşlik ettiği nadir bir fasiyal asimetri olgusu
Öz
Anahtar Kelimeler
References
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- Bawle EV, Conard J, Van Dyke DL, Czarnecki P, Driscoll DA. Seven new cases of Cayler cardiofacial syndrome with chromosome 22q11.2 deletion, including a familial case. Am J Med Genet 1998; 79: 406-10.
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- Joyce CA, Sharp A, Walker JM, Bullman H, Temple IK. Duplication of 7p12.1- p13, including GRB10 and IGFBP1, in a mother and daughter with features of Silver-Russell syndrome. Hum Genet 1999; 105: 273-80.
- Bonar BE, Owens RW. Bilateral congenital facial paralysis: review of the literature and a classification. Am J Dis Child 1929; 38: 1256-72.
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Details
Primary Language
Turkish
Subjects
-
Journal Section
-
Authors
Ayşegül Zenciroğlu
Ayşe Aksoy
Ramiz Gündüz
Publication Date
June 20, 2011
Submission Date
May 26, 2010
Acceptance Date
-
Published in Issue
Year 2011 Volume: 33 Number: 2