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Iranian Journal of Public Health، جلد ۲۸، شماره ۱-۴، صفحات ۵۱-۵۴
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عنوان انگلیسی CYTOGENETIC STUDY OF TURNER SYNDROME IN IRAN
چکیده انگلیسی مقاله Turner syndrome is one of the best known chromosome anomalies in human being, by an approximate incidence of 1/2500 female at birth. The cause is a chromosomal aberration, mainly with the karyotype 45, X. Ninety six patients aged 6 to 26 years with short stature were studied for chromosomal anomalies. Out of these 82 were phenotypically female and 14 phenotypically male. Twenty seven showed abnormal karyotypes, 15 were pure Turner with a chromosome complement of 45, X. Seven showed mosaiscim of 45, X/46, XX and 5 showed 45, X/46, XY cell lines. Most of the features of Turner’s syndrome were manifested in the fifteen 45, X Turners while the 45, X/46; XX did not show all the features due to the presence of a normal cell line. Out of the mosaics 45, X/46, XY, four had female phenotypes with normal genitalia while one had a male phenoytype with poorly developed male genitalia.
کلیدواژه‌های انگلیسی مقاله Turner syndrome, Chromosome anomaly
نویسندگان مقاله s y seyedna | s y seyedna


r خانی | r zakikhani


نشانی اینترنتی http://ijph.tums.ac.ir/index.php/ijph/article/view/1747
فایل مقاله اشکال در دسترسی به فایل - ./files/site1/rds_journals/86/article-86-350288.pdf
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زبان مقاله منتشر شده en
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نوع مقاله منتشر شده Articles
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