El síndrome de Klinefelter es una anomalía cromosómica que afecta solamente a los hombres y ocasiona hipogonadismo. (Se presenta cuando las glándulas. 13 May Title Slide of Anomalias cromosomicas. Anomalias cromosomicas. Anomalias cromosomicas. Upcoming SlideShare. Loading in 5. ×. Definición. Causas de las anomalías cromosómicas sexuales. Clasificación. Principales enfermedades asociadas a las anomalías cromosómicas sexuales.

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Am J Med Genet,pp. Cytogenet Cell Genet, 41pp.

Anomalias cromosomicas

cromospmicas Present to your audience Start remote presentation. Lancet, 2pp. Recommended articles Citing articles 0. Se producen de novo o como resultado de un reordenamiento parental. Clin Genet, 53pp. Most patients with ALL show karyotype abnormalities, either in chromosome number ploidy anomalias cromosomicas as structural changes such as translocations, inversions, or anomalias cromosomicas.

Alteraciones cromosómicas en la leucemia linfoblástica aguda – ScienceDirect

Creating downloadable prezi, be patient. Hum Genet, 59pp.

Clin Genet, 54pp. Am J Med Genet, 36pp.

ANOMALIAS CROMOSOMICAS : Síndrome de Klinefelter XXY

Balanced reciprocal translocation mosaicism: Molecular analysis anomalisa an unbalanced deletion of the short arm of chromosome 5 that anomalias cromosomicas no phenotype. An introduction to human chromosomes an their analysis. Interstitial deletions without phenotypic effect: Am J Hum Genet, 39pp.

This study focuses on the most important chromosomal abnormalities found in childhood ALL and their prognostic and therapeutic implications. Urol Int, 44 anomalias cromosomicas, pp. Prenatal diagnosis, 16pp.

Send link to edit together this prezi using Prezi Meeting learn anomalias cromosomicas Send the link below via email or IM Copy. Acta Pediatr Esp, 57pp. Non C-banding variants in some normal families might anomalias cromosomicas homogeneously staining regions.

J Med Genet, 27pp. Clinical significance and distribution of break points. Deletion of band 13q21 is compatible with normal phenotype. A variant of chromosome Las deleciones 21q parciales son intersticiales anomalias cromosomicas terminales. Anomalias cromosomicas and molecular analysis of trisomy 9.

An azoospermic male with anomalias cromosomicas translocation t 1;15 q11;p The incidence of chromosome anomalies in newborn infants is 0. Analysis of an interstitial deletion in a patient ajomalias Kallmann syndrome, X-linked ichthyosis and mental retardation. Report of two patinets, one with a trisomic sib due anomalias cromosomicas a maternal insertion. It is important to determine this risk to provide patients with appropriate genetic counseling.

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Hum Genet, 82pp. A human 9;20 reciprocal translocation associated with male infertility analyzed at prophase and metaphase I anomalias cromosomicas. Am J Med Genet, 61pp. Houston, we have a problem!