Síndrome de Turner
Twenty wholly studied patients with turne's phenotype, whose caryologic studies confirm the chromosomal abnormality, are presented. A review of the literature on the subject has been done. Finally, a discussion on the hypothesis over the origin of the chrosomal abnormality and its significance...
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Format: | Article |
Language: | English |
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Universidad Nacional de Colombia
1972-04-01
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Series: | Revista de la Facultad de Medicina |
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Online Access: | https://revistas.unal.edu.co/index.php/revfacmed/article/view/22053 |
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author | Emilio Yunis T. Emilia de la Cruz Germán Niño Murcia Myriam Leivovici |
author_facet | Emilio Yunis T. Emilia de la Cruz Germán Niño Murcia Myriam Leivovici |
author_sort | Emilio Yunis T. |
collection | DOAJ |
description | Twenty wholly studied patients with turne's phenotype, whose caryologic studies confirm the chromosomal abnormality, are presented. A review of the literature on the subject has been done. Finally, a discussion on the hypothesis over the origin of the chrosomal abnormality and its significance in the various Turner's phenotypes is presented. |
first_indexed | 2024-04-14T03:06:51Z |
format | Article |
id | doaj.art-3d07724e50b54122ad28e78dcaf6e0ea |
institution | Directory Open Access Journal |
issn | 0120-0011 2357-3848 |
language | English |
last_indexed | 2024-04-14T03:06:51Z |
publishDate | 1972-04-01 |
publisher | Universidad Nacional de Colombia |
record_format | Article |
series | Revista de la Facultad de Medicina |
spelling | doaj.art-3d07724e50b54122ad28e78dcaf6e0ea2022-12-22T02:15:42ZengUniversidad Nacional de ColombiaRevista de la Facultad de Medicina0120-00112357-38481972-04-0138214719419789Síndrome de TurnerEmilio Yunis T.0Emilia de la Cruz1Germán Niño Murcia2Myriam Leivovici3Universidad Nacional de ColombiaUniversidad Nacional de ColombiaUniversidad Nacional de ColombiaUniversidad Nacional de ColombiaTwenty wholly studied patients with turne's phenotype, whose caryologic studies confirm the chromosomal abnormality, are presented. A review of the literature on the subject has been done. Finally, a discussion on the hypothesis over the origin of the chrosomal abnormality and its significance in the various Turner's phenotypes is presented.https://revistas.unal.edu.co/index.php/revfacmed/article/view/22053síndrome de Noonansíndrome de Ullrichmonosomía Xenfermedades genéticas |
spellingShingle | Emilio Yunis T. Emilia de la Cruz Germán Niño Murcia Myriam Leivovici Síndrome de Turner Revista de la Facultad de Medicina síndrome de Noonan síndrome de Ullrich monosomía X enfermedades genéticas |
title | Síndrome de Turner |
title_full | Síndrome de Turner |
title_fullStr | Síndrome de Turner |
title_full_unstemmed | Síndrome de Turner |
title_short | Síndrome de Turner |
title_sort | sindrome de turner |
topic | síndrome de Noonan síndrome de Ullrich monosomía X enfermedades genéticas |
url | https://revistas.unal.edu.co/index.php/revfacmed/article/view/22053 |
work_keys_str_mv | AT emilioyunist sindromedeturner AT emiliadelacruz sindromedeturner AT germanninomurcia sindromedeturner AT myriamleivovici sindromedeturner |