Yardımcı Üreme Tekniği İle Olan Preterm İkiz Eşinde Tanımlanmış Bir Greig Sendromu Olgusu
Abstract
Keywords
References
- Biesecker LG. The Greig cephalopolysyndac- tyly syndrome. Orphanet J Rare Dis 2008; 24:10.
- Balk K, Biesecker LG.The Clinical Atlas Of Greig Cephalopolysyndactly Syndrome. Am J Med Genet A 2008; 146: 548-57.
- Biesecker LG.What you can learn from one gene : GL13. J Med Genet 2006; 43: 465- 69.
- Winter RM, Huson SM. Greig Cephalopoly- syndactly Syndrome: A possible mouse ho- mologue (xt- extratoes). Am j Med. Genet 1998; 31:93-8
- Marafie MJ, Temtamy SA, Rajaram U, al- Awadi SA, el-Badramany MH, Farag TI. Greig cephalopolysyndactyly syndrome with dysgenesis of the corpus callosum in a Bedouin family. Am j Med Genet 1996; 66: 261-64
- Wang CH, Tsai FJ, Shi YR. Greig Cephalo- polysyndactly Syndrome in a family. Acta Paediatr Taiwan 2006; 447: 97-9.
- Kunze J, Kaufmann HJ (1985). Greig cepha- lopolysyndactyly syndrome. Report of a spo- radic case. Helv Paediatr Acta 1985; 40:489- 95.
- Williams PG, Hersh JH, Yen FF, Barch MJ, Kleinert HE, Kunz J, Kalff-Suske M. Greig Cephalopolysyndactly Syndrome : Altered phenotype of a microdeletion syndrome due to presence of a cytogenetic abnormality. Clin Genet 1997; 52:436-41
Details
Primary Language
Turkish
Subjects
-
Journal Section
-
Authors
Nurdan Uraş
This is me
Ömer Erdeve
This is me
Şerife Suna Oğuz
This is me
Uğur Dilmen
This is me
Publication Date
April 1, 2009
Submission Date
December 13, 2014
Acceptance Date
-
Published in Issue
Year 2009 Volume: 62 Number: 4