Search Results - "Temocin, Kubra"

Clastogenicity of selective serotonin-reuptake inhibitors by Bozkurt, Gokay, Abay, Ercan, Ates, Ibrahim, Karabogaz, Goksel, Ture, Mevlut, Savran, Fatma Oguz, Palanduz, Sukru, Temocin, Kubra, Algunes, Cetin

“…Objective: Selective serotonin-reuptake inhibitors (SSRIs) are used in the treatment of various forms of psychiatric disorders. Preclinical studies in…”
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Fibular dimelia and mirror foot without associated anomalies by Bayram, H, Herdem, M, Temoçin, A K

“…Fibular dimelia with mirror foot is a rare anomaly that may be associated with additional anomalies such as ulnar dimelia, facial abnormalities and…”
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Tıbbi biyoloji ve genetik laboratuvar kitabı: Yrd. Doç. Dr. Nurhan Cücer, Uzm. Dr. A. Kübra Temoçin by Cücer, Nurhan, Temoçin, Aliye Kübra

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Ultrasonographic prenatal diagnosis of isolated acephaly by Unsal, Alparslan, Sezer, Selda Demircan, Meteoğlu, Ibrahim, Temoçin, Kübra, Karaman, Can Zafer

“…First trimester obstetric ultrasonography of a 32-year old female patient revealed a 13-week-old (according to the length of the femur and abdominal…”
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A rare cause of neonatal seizure: incontinentia pigmenti by Türkmen, Münevver, Eliaçik, Kayi, Temoçin, Kübra, Savk, Ekin, Tosun, Ayşe, Dikicioğlu, Emel

“…Incontinentia pigmenti (IP) is a rare genetic multisystem disorder that may affect many organs including the skin, bone, eyes and the central nervous system…”
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5-46-02 Family history in patients with low back pain by Turgut, Mehmet, Bayülkem, Kemal, Kübra Temoçin, A., Genel, Hülya

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Short rib-polydactyly syndrome: a case report by Türkmen, Münevver, Temoçin, Kübra, Acar, Cağlar, Levi, Edi, Karaman, Can, Inan, Gülten, Elçioğlu, Nursel

“…Short rib-polydactyly syndrome (SRPS) is a group of rare, lethal skeletal dysplasias characterized by short ribs and limbs, polydactyly, hypoplastic thorax and…”
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Partıal Deletıon Of Long Arm Of Chromosome 11 [Del(11) (Q24)] In A Patıent Presentıng Wıth Behavıoral Dısturbances by Avcı,Ayşe, Balat,Ayşe, Temoçın,A. Kübra, Demirhan,Osman

“…In this report we present a 10 year-old girl having behavioral disturbances and a deletion on the long arm of chromosome 11 involving the q24 region. We…”
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A case of spondylocostal dysostosis with a fra (5) (q32) by Satar, M, Temoçin, A K, Atici, A, Demirhan, O

“…Spondylocostal dysostosis is a rare hereditary syndrome with various costal and vertebral deformities. No chromosomal abnormalities in connection with this…”
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Lowe syndrome with anal atresia: A possible variant of OCRL? by Sönmez, Ferah, Temoçin, A Kübra, özkan, Seyhan B, Akçanal, Betül, Karaman, Can Z, Türkmen, Münevver, i̇nan, Gülten

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A case of ambiguous genitalia with unilateral amelia and unilateral peromelia of the upper limbs by TEMOĈIN, A. KüBRA, YüKSEL, BILGIN, TUNCER, RECEP, ÖZER, GüLER, ZORLUDEMIR, üNAL

“…A 7‐year‐old patient is reported with a 46,XY karyotype, ambiguous genitalia and unilateral amelia and unilateral peromelia of the upper limbs. The external…”
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Partıal Deletıon Of Long Arm Of Chromosome 11 [Del(11) (Q24)] In A Patıent Presentıng Wıth Behavıoral Dısturbances Osman Demırhan by Avcı,Ayşe, Balat,Ayşe, Temoçın,A. Kübra

“…In this report we present a 10 year-old girl having behavioral disturbances and a deletion on the long arm of chromosome 11 involving the q24 region. We…”
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Lowe syndrome with anal atresia: A possible variant of OCRL? by Sönmez, Ferah, Temoçin, A Kübra, özkan, Seyhan B, Akçanal, Betül, Karaman, Can Z, Türkmen, Münevver, i̇nan, Gülten

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Translokasyon tipi down sendromlu bir olguda konjenital hipotiroidizm by SOYLU, Semra, TÜRKMEN, Münevver, ULUCAN, Hakan, TEMOÇİN, A. Kübra, ÜNÜVAR, Tolga

“…Dismorfik yüz görünümü ve tiroid hormonu değerlerinde düşüklük saptanan kırk iki günlük kız bebekte; translokasyon tipi Down Sendromu ve hipotiroidi…”
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Seckel sendromu (iki olgu sunumu) by ALTINBAŞAK, Şakir, YEĞİN, Ayşegül, TEMOÇİN, A. Kübra, ALTINTAŞ, Derya V, EVLİYAOĞLU, Nurdan

“…Çukurova Üniversitesi Hastanesi Pediatri Polikliniğine getirilen ileri derecede mental retarde ve mikrosefalik iki olgu genetik yönden incelendi, Seckel…”
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