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Turner syndrome female with a small ring X chromosome lacking the XIST, an unexpectedly mild phenotype and an atypical association with alopecia universalis

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Year: 2004
Type: article
Study design: Case Report
Source: Annales de Génétique
DOI: 10.1016/j.anngen.2004.03.008
Authors: N. Bouayed Abdelmoula, M.F. Portnoï, A. Amouri, A. Arladan, M. Chakroun, A. Saad, M. Hchicha, H. Turki, T. Rebai
Institutions: University of Sfax, Faculty of Medicine of Sfax, Hôpital Saint-Antoine, Institut Pasteur de Tunis, Centre Hospitalier Universitaire Henri-Mondor, Hôpitaux Universitaires Henri-Mondor, Hôpital Farhat Hached, Hopital Universitaire Hedi Chaker
Language: English

Topic: Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities
Subfield: Genetics
Field: Biochemistry, Genetics and Molecular Biology
Domain: Life Sciences
SDG: Good health and well-being

Open Access status: closed
OpenAlex ID: W2007144364
FWCI:
Cites: 35
Cited by: 11
Related to: 10
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