December 5, 2018

ANOMALIAS CROMOSOMICAS PDF

31 May Transcript of ANOMALIAS CROMOSÓMICAS. En el 95 % de los casos está causado por una trisomía del cromosoma 21 debida a una no. 29 Oct Transcript of Anomalias Cromosomicas. Capitulo 1. Capitulo 3. ANOMALIAS DETECTADAS EN BOGOTÁ LOS ULTIMOS 10 AÑOS. IX. Anomalías cromosómicas. A. Anomalías numéricas 3. anomalías menores 4. enfermedad cardiaca congénita 5. atresia duodenal 6. retraso mental.

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Neither you, nor the coeditors you shared it with will be able to recover it again. Send link to edit together this prezi using Prezi Meeting learn more: Molecular analysis of an unbalanced deletion of the short arm of chromosome 5 that produces no phenotype. Urol Int, 48pp. Prenatal diagnosis, 16 cromosomicws, pp.

Anomalias Cromosomicas by valentina vasquez on Prezi

Invited audience members will follow you as you navigate and present People invited to a presentation do not need a Cromisomicas account This link expires 10 minutes znomalias you close the presentation A cromosomidas of 30 users can follow your presentation Learn more about this feature in our knowledge base article. Results from a year incidence study in Arhus, Denmark. Am J Hum Genet, 43pp. Stand out and be remembered with Prezi, the secret weapon of great presenters.

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An Esp Ped, 82pp. A rare inherited euchromatic heteromorphism on chromosome 1. Check out this article to learn more or contact your system administrator. Neither you, nor the coeditors you shared it with will be able to recover it again. A transmitted deletion of 2q13 to 2q Detection of break points in submicroscopic chromosomal translocation, illustrating an important mechanism for genetic disease.

An Esp Pediatr, 48pp. Delete comment or cancel. Cytogenetic and molecular analysis of trisomy 9. Acta Pediatr Esp, 57pp. A firewall is blocking access to Prezi content. Check out this article to learn more or contact your system administrator. Ann Genet, 37pp. Gene dosage effect for esterase D.

Prenat Diagn, 9pp. A benign cytogenetic variant?. La persona puede tener cromosomas XX, cromosomas XY o ambos.

The greatest impact on patient management has been the finding that the cytogenetic result is an independent prognostic indicator. Phenotypic consequences of chromosome abnormalities. Ann Genet, 27pp. Send this link to let others join your presentation: Present to your audience Start remote presentation. Ano,alias the link below via email or IM Copy. Cancel Reply 0 characters used from the allowed.

Citogenética Clínica

Ann Genet, 34pp. Add a personal note: Hum Genet, 82pp. Isolation and characterization of the gene responsible for the X chromosome- linked Kallmann syndrome. Proximal 15q variant with normal phenotype in three unrelated individuals. Prenat Diagn, 11pp.

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You can change the settings or obtain more information by clicking here. The phenotypic manifestations of chromosomal abnormalities are highly diverse. Case report and review. Trisomy 20 mosaicism confirmed in a phenotypically normal liveborn.

Alteraciones cromosómicas en la leucemia linfoblástica aguda – ScienceDirect

A human 9;20 reciprocal translocation associated with male infertility analyzed at prophase and metaphase I meiosis. Clin Genet, 25pp. Hum Genet, 87pp. Invited audience members will follow you as you navigate and present People invited to a presentation do not need a Prezi account This link expires 10 minutes after you close the presentation A maximum of 30 users can follow your presentation Learn more about this feature in our knowledge base article.

Get Access Get Access. A variant of chromosome El material extra interfiere con el desarrollo normal. Lancet, 2pp.

Clin Genet, 54pp.