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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Clases de citogenética de Dinulos — 2.ª parte

Full mosaic monosomy 22 in a child with DiGeorge syndrome facial appearance. Please log in to add your comment. Am J Med Genet, 69 cromospmicas, pp. To improve our services and products, we use “cookies” own or third parties authorized to show advertising related to client preferences through the analyses of navigation customer behavior. Isolation and characterization of the gene responsible for the X chromosome- linked Kallmann syndrome. Prenatal diagnosis, 16pp.

Gene dosage effect for esterase D. Endocr Metab Clin North Am, 25pp. Results from a year incidence study in Arhus, Denmark. A diagnosis at the end of the chromosomes. It is important to determine this risk to provide patients with appropriate genetic counseling.


Creating downloadable prezi, be patient. Am J Med Genet,pp. Clin Genet, 31pp. Add a personal note: Prenat Diagn, 9pp. An azoospermic male with reciprocal translocation t 1;15 q11;p Interstitial deletions without phenotypic effect: Prenat Diagn, 11pp. Stand out and be remembered with Prezi, the secret weapon of great presenters. Cytogenetic analysis of blast cells in childhood acute lymphoblastic leukemia has led to the recognition of specific non-random chromosomal abnormalities with prognostic value.

Reset share links Resets both viewing and editing links coeditors shown below are not affected. Send link to edit together this prezi using Prezi Meeting learn more: An Esp Pediatr, 48pp. Constrain to simple back and forward steps.

Cytogenetic and molecular analysis of trisomy 9. Este tipo generalmente es el resultado de un feto femenino que ha estado expuesto a excesivas hormonas masculinas antes del nacimiento.

J Med Genet, 40pp. Duplication of euchromatin without phenotypic effect: A firewall is blocking access to Prezi content. An Esp Pediatr, 49pp. Internal intersexuality masculine uterus and severe abnormality of the anterior chamber of the eye. Case report and review. Phenotypic consequences of chromosome abnormalities. Am J Med Genet, 56pp. Neither you, nor the coeditors you shared it with will be able to recover it again. Instituto Nacional de Salud. Hum Genet, 82pp.


Hum Genet, 80pp.

ANOMALIAS CROMOSÓMICAS by Daniel Redrobán on Prezi

Neither you, nor the coeditors you shared it with will be able to recover it again. Hum Genet, 71pp. Molecular screening for Yq microdeletion in men with idiopathic oligozoospermia and azoospermia. See more popular or the latest prezis.

Citogenética Clínica

J Med Genet, 31pp. Send this link to let others join your presentation: The use of telomere probes to investigate submicroscopic rearrangements associated with mental retardation. Urol Int, 44pp. Do you really want to delete this prezi? An anomlaias male with reciprocal translocation t 3;4 p21;q Am Heart J,pp.

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