Cargando…
A paternal t(6;22)(q25.3;p12) leading to a deleted and satellited der(6) in a short‐lived infant
BACKGROUND: Non‐acrocentric satellited chromosomes mostly result from familial balanced insertions or translocations with p12 or p13 of any acrocentric. Although all non‐acrocentrics have been involved, only 12 instances of chromosome 6 involvement are known. CASE PRESENTATION: A female infant exhib...
Autores principales: | Domínguez, María Guadalupe, Rivera, Horacio, Dávalos‐Pulido, Rosa María, Dávalos‐Rodríguez, Ingrid Patricia |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2020
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7439351/ https://www.ncbi.nlm.nih.gov/pubmed/32399990 http://dx.doi.org/10.1002/jcla.23355 |
Ejemplares similares
-
¡MS-DOS 6.22 fácil!
por: Fulton, Jennifer
Publicado: (1994) -
Using MS-DOS 6.22
por: Cooper, Jim
Publicado: (2002) -
Novel maternal duplication of 6p22.3-p25.3 with subtelomeric 6p25.3 deletion: new clinical findings and genotype–phenotype correlations
por: Zhang, Liyu, et al.
Publicado: (2023) -
A familial rearrangement(3;5;9) with paternal and maternal transmission leading to a duplication 3p/deletion 5p infant
por: Rivera, Horacio, et al.
Publicado: (2012) -
22q11.2 deletion detected by in situ hybridization in Mexican patients with velocardiofacial syndrome-like features
por: Ramírez-Velazco, Azubel, et al.
Publicado: (2018)