Cargando…
A female patient with retinoblastoma and severe intellectual disability carrying an X;13 balanced translocation without rearrangement in the RB1 gene: a case report
BACKGROUND: Female carriers of a balanced X; autosome translocation generally undergo selective inactivation of the normal X chromosome. This is because inactivation of critical genes within the autosomal region of the derivative translocation chromosome would compromise cellular function. We here r...
Autores principales: | Tsutsumi, Makiko, Hattori, Hiroyoshi, Akita, Nobuhiro, Maeda, Naoko, Kubota, Toshinobu, Horibe, Keizo, Fujita, Naoko, Kawai, Miki, Shinkai, Yasuko, Kato, Maki, Kato, Takema, Kawamura, Rie, Suzuki, Fumihiko, Kurahashi, Hiroki |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2019
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6896736/ https://www.ncbi.nlm.nih.gov/pubmed/31806026 http://dx.doi.org/10.1186/s12920-019-0640-2 |
Ejemplares similares
-
Molecular analysis of low‐level mosaicism of the IKBKG mutation using the X Chromosome Inactivation pattern in Incontinentia Pigmenti
por: Kawai, Miki, et al.
Publicado: (2020) -
An aggressive systemic mastocytosis preceded by ovarian dysgerminoma
por: Tsutsumi, Makiko, et al.
Publicado: (2020) -
Association between sites and severity of eczema and the onset of cow’s milk and egg allergy in children
por: Kawada, Shiori, et al.
Publicado: (2020) -
Palindrome-Mediated Translocations in Humans: A New Mechanistic Model for Gross Chromosomal Rearrangements
por: Inagaki, Hidehito, et al.
Publicado: (2016) -
Compound heterozygous TYK2 mutations underlie primary immunodeficiency with T-cell lymphopenia
por: Nemoto, Michiko, et al.
Publicado: (2018)