Cargando…
Subtelomeric study of 132 patients with mental retardation reveals 9 chromosomal anomalies and contributes to the delineation of submicroscopic deletions of 1pter, 2qter, 4pter, 5qter and 9qter
BACKGROUND: Cryptic chromosome imbalances are increasingly acknowledged as a cause for mental retardation and learning disability. New phenotypes associated with specific rearrangements are also being recognized. Techniques for screening for subtelomeric rearrangements are commercially available, al...
Autores principales: | Sogaard, Marie, Tümer, Zeynep, Hjalgrim, Helle, Hahnemann, Johanne, Friis, Birgitte, Ledaal, Paal, Pedersen, Vibeke Faurholt, Baekgaard, Peter, Tommerup, Niels, Cingöz, Sultan, Duno, Morten, Brondum-Nielsen, Karen |
---|---|
Formato: | Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2005
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1174871/ https://www.ncbi.nlm.nih.gov/pubmed/15904506 http://dx.doi.org/10.1186/1471-2350-6-21 |
Ejemplares similares
-
Chromosomal imbalance letter: Phenotypic consequences of combined deletion 8pter and duplication 15qter
por: Sheth, Frenny, et al.
Publicado: (2013) -
Gain of Chromosome 4qter and Loss of 5pter: An Unusual Case with Features of Cri du Chat Syndrome
por: Sheth, Frenny, et al.
Publicado: (2012) -
Trisomy 1q41-qter and monosomy 3p26.3-pter in a family with a translocation (1;3): further delineation of the syndromes
por: Cervantes, Alicia, et al.
Publicado: (2014) -
De Novo ring chromosome 11 and non-reciprocal translocation of 11p15.3-pter to 21qter in a patient with congenital heart disease
por: Peng, Ying, et al.
Publicado: (2015) -
The Facioscapulohumeral muscular dystrophy region on 4qter and the homologous locus on 10qter evolved independently under different evolutionary pressure
por: Rossi, Monica, et al.
Publicado: (2007)