Sevim Balci
Department of Clinical Genetics
Hacettepe University Medical Faculty
Ihsan Doğramaci Children's Hospital
Ankara
Turkey
Name/email consistency: high
- A 19-year follow-up of a patient with type 3 ectrodactyly-ectodermal dysplasia-clefting syndrome who developed non-Hodgkin lymphoma. Balci, S., Engiz, O., Okten, G., Sipahier, M., Gursu, G., Kandemir, B. Oral. Surg. Oral. Med. Oral. Pathol. Oral. Radiol. Endod (2009)
- A severely mentally and motor retarded girl with monosomy 3pter-->p25 and trisomy 8q24-->qter due to a familial reciprocal translocation t(3;8)(p25;q24). Balci, S., Aypar, E., Beksaç, M.S., Bartsch, O. Genet. Couns. (2009)
- A prenatally sonographically diagnosed conotruncal anomaly with mosaic type trisomy 21 and 22q11.2 microdeletion/DiGeorge syndrome. Balci, S., Altugan, F.S., Alehan, D., Aypar, E., Baltaci, V. Genet. Couns. (2009)
- Association of assisted reproductive technology with twinning and congenital anomalies. Balci, S., Engiz, O., Alikasifoglu, M., Esinler, I., Sinan Beksac, M. Indian. J. Pediatr (2008)
- Bilateral periventricular nodular heterotopia, severe learning disability, and epilepsy in a male patient with 46,XY,der(19)t(X;19) (q11.1-11.2;p13.3). Balci, S., Unal, A., Engiz, O., Aktas, D., Liehr, T., Gross, M., Mrasek, K., Saygi, S. Dev. Med. Child. Neurol (2007)
- Ring chromosome 4 and Wolf-Hirschhorn syndrome (WHS) in a child with multiple anomalies. Balci, S., Engiz, O., Aktaş, D., Vargel, I., Beksaç, M.S., Mrasek, K., Vermeesch, J., Liehr, T. Am. J. Med. Genet. A (2006)
- Partial trisomy (11;22) syndrome with manifestations of Goldenhar sequence due to maternal balanced t(11;22). Balci, S., Engiz, O., Yilmaz, Z., Baltaci, V. Genet. Couns. (2006)
- Balanced de novo translocation t(6;7)(p25;q31) and cleft palate as an isolated finding. Balci, S., Aypar, E., Son, Y.A., Beksaç, M.S. Genet. Couns. (2004)
