المؤلفون: Toruner, G. A., CinbiÅŸ, Mine, Bagcı, Gülseren, Semerci, Nur, Çetin, Gökhan Ozan

مصطلحات موضوعية: anteverted nostril, agenesis, article, birth weight, blepharophimosis, body height, body weight, C banding, case report, chromosome 14q, chromosome breakage, chromosome translocation, chromosome Xp, chromosome Yp, congenital heart malformation, corpus callosum, cytogenetics, DNA microarray, eye malformation, face dysmorphia, flatfoot, fluorescence in situ hybridization, gait disorder, gene deletion, gene duplication, growth retardation, head circumference, hearing impairment, hernia, heterochromatin

العلاقة: Clinical Dysmorphology; Makale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı; https://hdl.handle.net/11499/8798Test; https://doi.org/10.1097/MCD.0b013e32834d6ba3Test; 21; 37; 41; 2-s2.0-83255181192; WOS:000298148400010

الإتاحة: https://doi.org/10.1097/MCD.0b013e32834d6ba3Test
https://hdl.handle.net/11499/8798Test

المؤلفون: Yüksel, Selçuk, Herek, Duygu, Becerir, Tülay, Herek, Özkan, Özdemir, Özmert M. A., CinbiÅŸ, Mine, Semiz, Serap

مصطلحات موضوعية: Genel ve Dahili Tıp

العلاقة: Pamukkale Tıp Dergisi; Makale - Ulusal Hakemli Dergi - Kurum Öğretim Elemanı; https://hdl.handle.net/11499/42051Test; 84 - 86; 84; 86

الإتاحة: https://hdl.handle.net/11499/42051Test

المؤلفون: CinbiÅŸ, Mine, Semerci, C.Nur, Ullmann, R., Steininger, A., Bahce, M., YaÄŸcı, Baki, Özden, Serap

مصطلحات موضوعية: FISH, aCGH, Partial trisomy 12q, Subtelomeric 6p deletion, transcription factor FOXC1, article, case report, child, chromosome 12q, chromosome 6p, clinodactyly, comparative genomic hybridization, congenital heart malformation, ear malformation, eye malformation, female, fluorescence in situ hybridization, foot malformation, foxf2 gene, gene, gene deletion, genetic disorder, hearing loss, human, hypertelorism, karyotype 46,XX, lip malformation, low set ear, lower lip, mental deficiency

العلاقة: American Journal of Medical Genetics, Part A; Makale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı; https://hdl.handle.net/11499/6577Test; https://doi.org/10.1002/ajmg.a.33383Test; 152; 1724; 1729; 2-s2.0-77954118855; WOS:000280115000045

الإتاحة: https://doi.org/10.1002/ajmg.a.33383Test
https://hdl.handle.net/11499/6577Test

المؤلفون: Erdogan-Bakar, E., CinbiÅŸ, Mine, Özyürek, H., KiriÅŸ, N., AltunbaÅŸak, Åž., Anlar, B.

مصطلحات موضوعية: Learning, female, heredity, Cognition, Follow-Up Studies, Humans, Male, Cognitive, Mental, Neurofibromatosis type 1, NF1, adolescent, Neurofibromatosis 1, Orientation, Severity of Illness Index, Siblings, Visual Perception, Young Adult, Wechsler Intelligence Scale, adult, arithmetic, article, attention deficit disorder, child, controlled study, environmental factor, human, intelligence, major clinical study, mental deficiency

العلاقة: Turkish Journal of Pediatrics; Makale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı; https://hdl.handle.net/11499/6654Test; 51; 565; 571; 2-s2.0-76649116229; WOS:000274692900007

الإتاحة: https://hdl.handle.net/11499/6654Test

المؤلفون: KıroÄŸlu, Yılmaz, CinbiÅŸ, Mine, Bican, Mevlüt, Polat, Aziz

مصطلحات موضوعية: Hematoloji, Tıbbi AraÅŸtırmalar Deneysel, Pediatri

العلاقة: Pamukkale Tıp Dergisi; Makale - Ulusal Hakemli Dergi - Kurum Öğretim Elemanı; https://hdl.handle.net/11499/41377Test; 109 - 112; 109; 112

الإتاحة: https://hdl.handle.net/11499/41377Test

المؤلفون: Candemir, MaÅŸallah, Halis, Hülya, Polat, Aziz, Ergin, Hacer, Kılıç, Ä°lknur, Semiz, Serap, CinbiÅŸ, Mine

مصطلحات موضوعية: Geriatri ve Gerontoloji, Tıbbi AraÅŸtırmalar Deneysel, Pediatri, Ãœroloji ve Nefroloji

العلاقة: Adnan Menderes Ãœniversitesi Tıp Fakültesi Dergisi; Makale - Ulusal Hakemli Dergi - Kurum Öğretim Elemanı; https://hdl.handle.net/11499/41040Test; 39 - 43; 39; 43

الإتاحة: https://hdl.handle.net/11499/41040Test

المؤلفون: Ergin, Hacer, DaÄŸdeviren, Erol, Polat, Aziz, Kılıç, Ä°lknur, Semiz, Serap, CinbiÅŸ, Mine

مصطلحات موضوعية: Hematoloji, Pediatri, Solunum Sistemi

العلاقة: Adnan Menderes Ãœniversitesi Tıp Fakültesi Dergisi; Makale - Ulusal Hakemli Dergi - Kurum Öğretim Elemanı; https://hdl.handle.net/11499/40917Test; 29 - 32; 29; 32

الإتاحة: https://hdl.handle.net/11499/40917Test

المؤلفون: Oguzkan, S., CinbiÅŸ, Mine, Ayter, Şükriye, Anlar, Banu, Aysun, Sabiha

مصطلحات موضوعية: Pedigree, Neurofibromatosis type 1, Polymerase Chain Reaction, Polymorphism, Genetic, Turkey, gene expression, gene location, gene mutation, gene sequence, genetic analysis, genetic code, genetic counseling, Molecular analysis, Presymptomatic diagnosis, amino acid, gene product, messenger RNA, neurofibromin, genetic polymorphism, human, human cell, iris disease, male, marker gene, microsatellite marker, neurofibroma, neurofibromatosis, prenatal diagnosis, relative

العلاقة: Turkish Journal of Pediatrics; Makale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı; https://hdl.handle.net/11499/5244Test; 45; 192; 197; 2-s2.0-0242607922; WOS:000187576000002

الإتاحة: https://hdl.handle.net/11499/5244Test

المؤلفون: CinbiÅŸ, Mine, Herek, Özkan

مصطلحات موضوعية: Hepatic dislocation, Congenital diaphragmatic eventration, Heterotaxy, abdominal radiography, article, case report, congenital diaphragm hernia, Fallot tetralogy, heterotaxy syndrome, human, infant, liver disease, male, priority journal, respiratory distress, situs inversus, thorax radiography, computer assisted tomography, congenital malformation, diaphragm, letter, liver, radiography, Humans, Tomography, X-Ray Computed

العلاقة: Clinical Dysmorphology; Makale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı; https://hdl.handle.net/11499/5400Test; https://doi.org/10.1097/00019605-200207000-00013Test; 11; 213; 214; 2-s2.0-0036018140; WOS:000176926300013

الإتاحة: https://doi.org/10.1097/00019605-200207000-00013Test
https://hdl.handle.net/11499/5400Test

المؤلفون: Bostancı, Ä°lknur, SarıoÄŸlu, Akile, AkÅŸit, Arif, CinbiÅŸ, Mine, Akalın, Necdet, Ergin, Hacer

مصطلحات موضوعية: neonatal goiter, maternal drug usage, iodine-induced hypothyroidism

العلاقة: JOURNAL OF PEDIATRIC ENDOCRINOLOGY & METABOLISM; Makale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı; https://hdl.handle.net/11499/25501Test; https://doi.org/10.1515/jpem-2001-0815Test; 14; 1161; 1162; 2-s2.0-0034789205; WOS:000171224200014

الإتاحة: https://doi.org/10.1515/jpem-2001-0815Test
https://hdl.handle.net/11499/25501Test