Zobrazeno 1 - 9
of 9
pro vyhledávání: '"Kübra TEMOÇiN"'
Autor:
Dilara SÜLEYMANOVA, Kübra TEMOÇiN
Publikováno v:
European Journal of Therapeutics. 6:116-120
Two patients who applied to our Genetics Unit with multiple congenital anomalies were examined for pedigree and cytogenetical analyses. The patients were diagnosed as Multiple Pterygium Syndrome(MPS) and medical genetic counselling was given to the p
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6ff29e929f8811155f28df634dd2eeff
https://doi.org/10.58600/eurjther.1995-6-1-1568-arch
https://doi.org/10.58600/eurjther.1995-6-1-1568-arch
Autor:
Ferah Sönmez, Betul Akcanal, Münevver Türkmen, A. Kübra Temoçin, Gülten Inan, Seyhan B. Özkan, Can Zafer Karaman
Publikováno v:
Pediatrics International. 45:201-204
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::451c09ad1e1a8900b1739db5b4c8939d
https://doi.org/10.1046/j.1442-200x.2003.01697.x
https://doi.org/10.1046/j.1442-200x.2003.01697.x
Autor:
Alparslan, Unsal, Selda Demircan, Sezer, Ibrahim, Meteoğlu, Kübra, Temoçin, Can Zafer, Karaman
Publikováno v:
Diagnostic and interventional radiology (Ankara, Turkey). 13(4)
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 circumference) intrauterine live pregnancy with the absence of the fetal head. Medical abortus was pe
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::47609adff5e64637ce5c7b1bf4904b29
https://pubmed.ncbi.nlm.nih.gov/18092292
https://pubmed.ncbi.nlm.nih.gov/18092292
Publikováno v:
The Turkish journal of pediatrics. 49(3)
Incontinentia pigmenti (IP) is a rare genetic multisystem disorder that may affect many organs including the skin, bone, eyes and the central nervous system. Central nervous system manifestations are seen in 30% of cases with seizures and mental reta
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::1e51c288aa95d42324276d66dddc0f50
https://pubmed.ncbi.nlm.nih.gov/17990592
https://pubmed.ncbi.nlm.nih.gov/17990592
Autor:
Münevver, Türkmen, Kübra, Temoçin, Cağlar, Acar, Edi, Levi, Can, Karaman, Gülten, Inan, Nursel, Elçioğlu
Publikováno v:
The Turkish journal of pediatrics. 45(4)
Short rib-polydactyly syndrome (SRPS) is a group of rare, lethal skeletal dysplasias characterized by short ribs and limbs, polydactyly, hypoplastic thorax and visceral anomalies. Our case had coarsening of facial features, low-set ears, lobulated to
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::73c84613657dac9350693ce6247ebc97
https://pubmed.ncbi.nlm.nih.gov/14768808
https://pubmed.ncbi.nlm.nih.gov/14768808
Publikováno v:
Journal of the Neurological Sciences. 150:S335
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a3f89a78d1b1bac094c86a72923d6f0d
https://doi.org/10.1016/s0022-510x(97)86541-0
https://doi.org/10.1016/s0022-510x(97)86541-0
Akademický článek
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Akademický článek
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Publikováno v:
In Journal of the Neurological Sciences 1997 150 Supplement 1:S335-S335