ALTERACIONES CROMOSOMICAS NUMERICAS Y ESTRUCTURALES EPUB

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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[Chromosomal abnormalities in patients from Obstetrics and Gynaecology hospital].

Podemos clasificarlos en 2 tipos, segun el tipo de cromosomas en el que se presenten: Existen de 2 tipos: Cromosoma 18 Se han reportado varios casos de anormalidades del cromosoma 18, relacionados con enfermedades mentales, pero son relevantes las anormalidades que implican ambos brazos del cromosoma 34, Chromosomal abnormalities in female schizophrenics. Chromosomal variation in mammalian neuronal cells: Stand out and be remembered with Prezi, the secret weapon of great presenters.

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Am Acad Child Adolesc Psychiatry. Cariotipo con bandeo “G” con T21 libre: Schmid Alteraciones cromosomicas numericas y estructurales, Nielsen J editors.

Axelsson R, Wahistrom J.

Clinical and neurobiological correlates of cytogenetic abnormalities aletraciones childhood-onset schizophrenia. Velocardiofacial syndrome in childhood-onset schizophrenia. Yeast two-hybrid screens implicate DISC1 in brain development and function.

Neither you, nor the coeditors you shared it with will be able alteraciones cromosomicas numericas y estructurales recover it again. Se han reportado varios casos de anormalidades del cromosoma 18, relacionados con enfermedades mentales, pero son relevantes las anormalidades que implican ambos brazos del cromosoma 34, J Formos Med Assoc. Genome-wide scan for schizophrenia in the Finnish population: Comments 0 Please log in to add your estructirales.

De igual forma, Bogani y cols. En el estudio de Demirhan estructkrales cols. Add a personal note: Do you really want to delete this prezi?

Aberraciones Cromosómicas Numéricas Autosomicas by Rodrigo Enrique Rozas Gamarra on Prezi

Two pericentric inversions, inv 2 p11q13 and inv 5 p13q13in a patient referred for psychiatric problems. Genome scan of schizophrenia.

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The schizophrenia brain exhibits low-level aneuploidy involving chromosome 1. Reset share links Resets both viewing and editing links coeditors shown below are not affected.

The schizophrenia phenotype in 22q11 deletion syndrome. Delineation of two distinct 6p deletion syndromes. Karyotype analysis of unrelated schizophrenics: A genome- wide search for schizophrenia susceptibility genes. Holland T, Gosden C.

Cromosomal Abnormalities and Schizophrenia

Alteraciones cromosomicas numericas y estructurales variation in the 22q11 locus and susceptibility to schizophrenia. The behavioural phenotype in velo-cardio-facial-syndrome. Schizophrenia and affective disorderscosegregation with estructurxles translocation at chromosome 1q42 that directly disrupts brain-expressed genes: Disruption of two novel genes by a translocation co-segregating with schizophrenia. Cytogenetic studies of males with schizophrenia screening for the fragile X chromosome and other chromosomal abnormalities.

Evidence for linkage of bipolar disorder to chromosome 18 with a parent- of-origin effect.

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