Detection of Turner Syndrome by Quantitative {PCR} of \textit{{SHOX}} and \textit{{VAMP}7} Genes
Ibarra Ramírez, Marisol y Zamudio Osuna, Michelle Jesús y Campos Acevedo, Luis Daniel y Gallardo Blanco, Hugo Leonid y Cerda Flores, Ricardo Martín y Rodríguez Sánchez, Irám Pablo y Martínez de Villarreal, Laura Elia (2015) Detection of Turner Syndrome by Quantitative {PCR} of \textit{{SHOX}} and \textit{{VAMP}7} Genes. Genetic Testing and Molecular Biomarkers, 19 (2). pp. 88-92. ISSN 1945-0265, 1945-0257
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Resumen
Turner syndrome (TS) affects 1 in 2500/3000 liveborn girls and is characterized by short stature, gonadal dysgenesis, pterygium colli, cubitus valgus, and a low hairline (Wiedemann and Glatzl, 1991; Ranke and Saenger, 2001; Pinsker, 2012). It is caused by partial or total loss of the second sex chromosome (Ford et al., 1959; Sybert and McCauley, 2004). Complete monosomy X (45,X) represents 50–60% of all cases, while mosaics of two or more cell lines and structural aberrations (mostly Xq isochromosomes) account for the remaining 40–50% (Sybert and McCauley, 2004).
| Tipo de elemento: | Article | ||||||||||||||||||||||||
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| Palabras claves no controlados: | Chromosomes, Human, X, Early Diagnosis, Gene Dosage, Gene Expression Profiling, Genes, X-Linked, Genes, sry, Genetic Testing, Homeodomain Proteins, Karyotyping, Mexico, Monosomy, Neonatal Screening, R-SNARE Proteins, RNA, Long Noncoding, Real-Time Polymerase Chain Reaction, Short Stature Homeobox Protein, Turner Syndrome, Ubiquitin-Activating Enzymes | ||||||||||||||||||||||||
| Materias: | CONACYT > Medicina y Ciencias de la Salud | ||||||||||||||||||||||||
| Divisiones: | Medicina | ||||||||||||||||||||||||
| Usuario depositante: | Dr.C. Hugo Gallardo Blanco | ||||||||||||||||||||||||
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| Fecha del depósito: | 23 Sep 2026 15:15 | ||||||||||||||||||||||||
| Última modificación: | 23 Sep 2026 15:15 | ||||||||||||||||||||||||
| URI: | http://eprints.uanl.mx/id/eprint/31434 |
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