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1 . Academic Journal
Genetic Counseling in a Case of a Pregnant Woman with Goldenhar Syndrome (Oculoauriculovertebral Spectrum)
저자
by
Aslıhan Yazıcıoğlu
;
Özge Senem Yücel
;
İlker Selçuk
;
Gökhan Boyraz
;
Mert Turğal
, et al.
소스
Gynecology Obstetrics & Reproductive Medicine, Vol 18, Iss 2 (2012)
Open Access (DOAJ)
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7 . Academic Journal
Prenatally Diagnosed Ureteropelvic Junction Obstruction in Three Siblings of one Family: A Case Report
저자
by
Sinan Beksaç
;
Sevim Balcı
;
Zuhal Yapıcı
;
Özgür Özyüncü
.
소스
Gynecology Obstetrics & Reproductive Medicine, Vol 14, Iss 3 (2008)
Open Access (DOAJ)
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6 . Academic Journal
Succesful Management of the Pregnancy Complicated with Thrombophilia, Uterine Unicollis and Previous Pregnancy Loss: A Case Report
저자
by
Sertaç Esin
;
Sinan Beksaç
;
Sevim Balcı
.
소스
Gynecology Obstetrics & Reproductive Medicine, Vol 12, Iss 3 (2006)
Open Access (DOAJ)
Find it @ DONGA
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5 . Academic Journal
Selective Feticide of The Aneuploid Fetus in a Twin Pregnancy: A Case Reports
저자
by
Sinan Beksaç
;
Tülay Özlü
;
Sevim Balcı
;
Mehmet Alikaşifoğlu
;
Nur Çakar
.
소스
Gynecology Obstetrics & Reproductive Medicine, Vol 12, Iss 1 (2006)
Open Access (DOAJ)
Find it @ DONGA
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RefWorks
7 .
Imaging Findings of Fetal-Neonatal Ovarian Cysts Complicated With Ovarian Torsion and Autoamputation
저자
by
Sevim Balci
;
Hatice Nursun Ozcan
;
Arbay O. Ciftci
;
Altan Güneş
;
Saniye Ekinci
, et al.
소스
American Journal of Roentgenology
. 205:185-189
Web of Science
Scopus
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7 .
Mandibuloacral dysplasia and LMNA A529V mutation in Turkish patients with severe skeletal changes and absent breast development
저자
by
Askin Sen
;
Leyla Ozer
;
Evrim Unsal
;
Volkan Baltaci
;
Sevim Balci
, et al.
소스
Clinical dysmorphology
. 25(3)
Scopus
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7 .
Familial ring (18) mosaicism in a 23-year-old young adult with 46,XY,r(18) (::p11→q21::)/46,XY karyotype, intellectual disability, motor retardation and single maxillary incisor and in his phenotypically normal mother, karyotype 47,XX,+r(18)(::p11→q21::)
저자
by
Celal Tümer
;
Oliver Bartsch
;
Sevim Balci
;
Çiğdem Tepe Karaca
.
소스
American Journal of Medical Genetics Part A
. 155:1129-1135
Web of Science
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6 .
Disruption of ALX1 Causes Extreme Microphthalmia and Severe Facial Clefting: Expanding the Spectrum of Autosomal-Recessive ALX-Related Frontonasal Dysplasia
저자
by
Safak Gucer
;
Nurten A. Akarsu
;
Ferdinand von Eggeling
;
Ozgur Deren
;
Dilek Aktas
, et al.
소스
The American Journal of Human Genetics
. 86(5):789-796
Full Text (ScienceDirect)
Full Text (ScienceDirect O/A)
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7 .
A case of Carpenter syndrome diagnosed in a 20-week-old fetus with postmortem examination
저자
by
T. Haytoglu
;
Sevim Balci
;
Muzaffer Eryilmaz
;
B Onol
.
소스
Clinical Genetics
. 51:412-416
Web of Science
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6 .
Corneal opacity, microphthalmia, mental retardation, microcephaly and generaIized muscular spasticity associated with hypergIycinemia
저자
by
T. Firat
;
Burhan Say
;
Sevim Balci
.
소스
Clinical Genetics
. 5:36-39
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