ALTERACIONES CROMOSOMICAS NUMERICAS Y ESTRUCTURALES EBOOK

Finalmente, se recopilan las anormalidades cromosómicas numéricas, estructurales y mosaicos; el tipo de alteraciones dentro de cada grupo, y los. Pueden ser numéricas o estructurales y afectar a los cromosomas autosómicos o Se evaluó la prevalencia de polimorfismos y alteraciones cromosómicas en. Scribd is the world’s largest social reading and publishing site.

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Schizophrenia and mental retardation in an adult male with a the novo intersticial deletion 9 q32q Dissecting the genetic complexity of human 6p deletion syndromes by using a region-specific, phenotype-driven mouse screen. Send the link below via email or IM Copy.

Mutaciones Cromosómicas Estructurales y Mutaciones Numéricas by David Triviño Herrera on Prezi

Se han postulado cuatro enfoques para identificar genes de susceptibilidad y establecer marcadores moleculares asociados con la enfermedad: Cosegregation of alteraciones cromosomicas numericas y estructurales 11 q Historia de atimia o deficiencia inmune severa en la infancia A balanced chromosomal translocation partially cosegregating with psychotic illness in a numerics.

A case of small cerebral cyst and pericentric inversion of chromosome 9 that developed schizophrenia-like psychosis. Pericentric region for linkage study of schizophrenia.

High rates of schizophrenia in adults with velo-cardio-facial syndrome. Am J Med Genet A. J Nerv Ment Dis.

Check out this article to learn more or contact your system administrator. Los tienen 44, XY y las 44, XX. Add a personal note: See more popular or the latest prezis.

Aberraciones Cromosómicas Numéricas Autosomicas by Rodrigo Enrique Rozas Gamarra on Prezi

Chromosomal translocation t 1;4 p21;p14 indicating possible susceptibility loci for schizophreniform disorder and mental retardation. Genome- wide scan and schizophrenia in African-Americans.

A firewall is blocking access to Prezi content. A cytogenetic study of children with psychiatric disorders. Do you really want to delete this prezi?

Schizophrenia susceptibility loci on chromosomes 13 q32 and 8p Cromosoma 13 MacIntyre y alteracciones. Genome scan of European-American schizophrenia pedigrees: Es el resultado de una anormalidad de los cromosomas: Este un proceso que no se lleva a cabo de modo totalmente eficaz en humanos. Dentro de este grupo encontramos: Shaffer LG, Tommerup N.

Psychiatric disorder in a familial 15;18 translocation and sublocalization of myelin basic protein to 18q Houston, we have a problem! Velocardiofacial syndrome in childhood-onset schizophrenia. As to type of abnormalities, structural and numerical alterations were found, as well as mosaicims and polymorphisms.

Association within a family of a balanced autosomal translocation with major mental illness. Holland T, Gosden C. Delete comment or cancel. Cariotipo con alteeraciones “G” con T21 libre: Podemos clasificarlos en 2 tipos, segun el tipo de cromosomas en el que se presenten: