De novo paracentric inversion in an X chromosome.
AUTOR(ES)
Herr, H M
RESUMO
A 10 1/2 year old female with skeletal abnormalities was referred for genetic consultation because of learning disabilities and a suggestion of 'Turner-like' stigmata. Cytogenetic analysis revealed a paracentric inversion of an X(q13.1q26.1) chromosome.
ACESSO AO ARTIGO
http://www.pubmedcentral.nih.gov/articlerender.fcgi?artid=1049401Documentos Relacionados
- Pregnancy wastage associated with paracentric inversion of chromosome 13.
- Familial paracentric inversion of chromosome 15 (q15q24).
- Non-disjunction of an unusual X chromosome.
- The Relationship of Crossing over to Chromosome Synapsis in a Short Paracentric Inversion
- Genes for intelligence on the X chromosome.
