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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Main Authors: Emilio Yunis T., Emilia de la Cruz, Germán Niño Murcia, Myriam Leivovici
Format: Article
Language:English
Published: Universidad Nacional de Colombia 1972-04-01
Series:Revista de la Facultad de Medicina
Subjects:
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.
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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