Cargando…
Identification and clinical evaluation of segments of homozygosity, uniparental disomy and complex chromosomal abnormalities revealed by copy-number SNP arrays
Autores principales: | Wang, Jia-Chi, Ross, Leslie, Mahon, Loretta W, Owen, Renius, Hemmat, Morteza, Wang, Boris T, El Naggar, Mohammed, Kopita, Kimberly A, Haddadin, Mary, Boyar, Fatih Z, Anguiano, Arturo, Strom, Charles M, Sahoo, Trilochan |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2014
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4043653/ http://dx.doi.org/10.1186/1755-8166-7-S1-O4 |
Ejemplares similares
-
Genotype-phenotype analysis of recombinant chromosome 4 syndrome: an array-CGH study and literature review
por: Hemmat, Morteza, et al.
Publicado: (2013) -
Abnormalities in spontaneous abortions detected by G-banding and chromosomal microarray analysis (CMA) at a national reference laboratory
por: Wang, Boris T, et al.
Publicado: (2014) -
Large heterozygous deletion and uniparental disomy masquerading as homozygosity in CHKB gene
por: Wu, Tenghui, et al.
Publicado: (2023) -
Cytogenetic contribution to uniparental disomy (UPD)
por: Liehr, Thomas
Publicado: (2010) -
Short stature, digit anomalies and dysmorphic facial features are associated with the duplication of miR-17 ~ 92 cluster
por: Hemmat, Morteza, et al.
Publicado: (2014)