Rare X Chromosome Abnormalities in Systemic Lupus Erythematosus and Sjögren's Syndrome
Objective: Sjögren's syndrome (SS) and systemic lupus erythematosus (SLE) are related by clinical and serologic manifestations as well as genetic risks. Both diseases are more commonly found in women than in men, at a ratio of ~10 to 1. Common X chromosome aneuploidies, 47,XXY and 47,XXX, are e...
- Autores:
- Tipo de recurso:
- Fecha de publicación:
- 2017
- Institución:
- Universidad del Rosario
- Repositorio:
- Repositorio EdocUR - U. Rosario
- Idioma:
- eng
- OAI Identifier:
- oai:repository.urosario.edu.co:10336/23033
- Acceso en línea:
- https://doi.org/10.1002/art.40207
https://repository.urosario.edu.co/handle/10336/23033
- Palabra clave:
- Article
Chromosome mosaicism
Cohort analysis
Controlled study
Epilepsy
Female
Human
Karyotyping
Major clinical study
Mosaicism
Oligomenorrhea
Priority journal
Single nucleotide polymorphism
Sjoegren syndrome
Systemic lupus erythematosus
Thyroid disease
X chromosome aberration
Allele
Bayes theorem
Gene dosage
Genetics
Karyotype
Lupus Erythematosus, Systemic
Sex chromosome aberration
Sex Chromosome Disorders of Sex Development
Sjogren's Syndrome
Statistics and numerical data
Trisomy
Turner syndrome
X chromosome
Alleles
Bayes Theorem
Female
Gene Dosage
Humans
Karyotype
Lupus Erythematosus, Systemic
Mosaicism
Sex Chromosome Aberrations
Sex Chromosome Disorders of Sex Development
Sjogren's Syndrome
Trisomy
Turner Syndrome
XX
Single Nucleotide
Human
X
Karyotype 46
Chromosomes
Polymorphism
- Rights
- License
- Abierto (Texto Completo)