Zobrazeno 1 - 10
of 18
pro vyhledávání: '"Nail Alp"'
Autor:
Turgay Budak, Mahmut Balkan, Hilmi Isi, M. Nail Alp, Mehmet Fidanboy, Sevgi Kalkanli, Halit Akbas
Publikováno v:
Journal of Pediatric Genetics. :243-246
We report a case of complete tetraploidy in amniotic fluid culture obtained at 17 wk of pregnancy. Amniocentesis was performed in this pregnancy because of a high-risk maternal serum screening result and abnormal ultrasound findings. Amniotic fluid w
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::52a8f8e20f0403934d8f21c565912876
https://doi.org/10.3233/pge-12039
https://doi.org/10.3233/pge-12039
Publikováno v:
Turkish Journal of Obstetrics and Gynecology, Vol 7, Iss 2, Pp 145-148 (2010)
Balanced autosomal translocations are unusually observed in the patients with hypogonadotropic hypogonadism. The patient with hypogonadotropic hypogonadism had balanced reciprocal translocation involving chromosomes 8 and 9. The patient’s father, t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doajarticles::3ee3b364160b358b87b787ae3e25f0ba
http://www.tjoddergisi.org/archives/archive-detail/article-preview/46-xx-del8q22-der9-t89q22p24-balanced-translocatio/9331
http://www.tjoddergisi.org/archives/archive-detail/article-preview/46-xx-del8q22-der9-t89q22p24-balanced-translocatio/9331
Publikováno v:
Journal of Genetic Counseling. 19:241-246
This study investigated parental decision-making to terminate or continue a pregnancy after prenatal diagnosis of a chromosomal abnormality among a sample of patients in Southeast Turkey. Between 2004 and 2007, 1068 amniocentesis tests were performed
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::732a6319e5aa11f6f150123d3bd76278
https://doi.org/10.1007/s10897-009-9275-3
https://doi.org/10.1007/s10897-009-9275-3
Publikováno v:
Dicle Medical Journal, Vol 35, Iss 1, Pp 61-64 (2008)
In this study, we are presenting the results of cytogenetic analysis and molecular cytogenetic analysis of the couple and their family, who were referred to our genetic diagnostic laboratory with two abortions in their reproductive history. We found
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doajarticles::8ae6a5b669fa4dbc22bb1c9e98c01307
http://4181.indexcopernicus.com/fulltxt.php?ICID=887354
http://4181.indexcopernicus.com/fulltxt.php?ICID=887354
Publikováno v:
Dicle Medical Journal, Vol 34, Iss 3, Pp 187-190 (2007)
In this study, we evaluated a total of 481 amniocentesis , cordocentesis and corion villi sample specimens from patients who were referred to the Prenatal Diagnostic Laboratory of Department of Medical Biology and Genetics Department of Medical Facul
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doajarticles::36152f71b0def77d9b47a59e2bb2ec60
http://4181.indexcopernicus.com/fulltxt.php?ICID=887704
http://4181.indexcopernicus.com/fulltxt.php?ICID=887704
Autor:
M. Nail Alp, Diclehan Oral
Publikováno v:
Dicle Medical Journal, Vol 33, Iss 2, Pp 71-80 (2006)
The aim of this study was to determine the chromosomal abberations and their incidence in non-consanguineous couples with a history of two or more than two spontaneous abortion. In the study, we carried out cytogenetic analysis on 434 couples. Patien
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doajarticles::8eeb6a0d0d767bc6c6fb3337382756fb
http://4181.indexcopernicus.com/fulltxt.php?ICID=888065
http://4181.indexcopernicus.com/fulltxt.php?ICID=888065
Publikováno v:
Dicle Medical Journal, Vol 32, Iss 3, Pp 149-152 (2005)
Case was 14 years-old girl having complaints of growth retardations and primary amenorrhea. In the physical and gynecological examinations; her height and weight were 130 cm and 45 kg, respectively and secondary sex characteristics were infantile and
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doajarticles::bcad721c27af4f087a260e0fd63f7e41
http://4181.indexcopernicus.com/fulltxt.php?ICID=888055
http://4181.indexcopernicus.com/fulltxt.php?ICID=888055
Publikováno v:
Dicle Medical Journal, Vol 33, Iss 4, Pp 256-258 (2006)
The Marfan syndrome is an inherited, autosomal dominant disorder that affects the skeletal, ocular and cardiovascular systems. The patient had clinical diagnosis of Marfan syndrome in the Department of Endocrinology. Chromosome analysis was performed
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doajarticles::c732cad0e9453ab7a838edb5ef67dc40
http://4181.indexcopernicus.com/fulltxt.php?ICID=888011
http://4181.indexcopernicus.com/fulltxt.php?ICID=888011
Publikováno v:
Dicle Medical Journal, Vol 33, Iss 2, Pp 98-100 (2006)
Chromosome analysis and buccal smear were performed to two siblings refered to Genetic Laboratory of Medical Biology Department with pre-diagnosis of Ambiguos Genitalia. The patients were clinically examined in the Department of Child Surgery. For ch
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doajarticles::d518b0398ba25720a7b626eff238d1ff
http://4181.indexcopernicus.com/fulltxt.php?ICID=888075
http://4181.indexcopernicus.com/fulltxt.php?ICID=888075
Autor:
Mahmut Balkan, Selçuk Otçu, Hilmi İsi, Diclehan Oral, Ayşegül Türkyılmaz, Selda Şimşek, Nail Alp, Turgay Budak
Publikováno v:
Dicle Medical Journal, Vol 31, Iss 2, Pp 65-67 (2004)
40 days old case who were diagnosed with ambigious genitalia were sentto laboratory of cytogenetics. Mother was 26 years old and have to alivechildren and case were the second child and applied to Child SurgeryDepartment due to continiously vomiting
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doajarticles::9354601d12d5acc3bd08c8d5b8316e0a
http://4181.indexcopernicus.com/fulltxt.php?ICID=887925
http://4181.indexcopernicus.com/fulltxt.php?ICID=887925