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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Internal intersexuality masculine uterus and severe abnormality of the anterior chamber of the eye. First report in North America, 37pp.

J Med Genet, 40pp. Molecular screening for Yq microdeletion in men with idiopathic oligozoospermia and azoospermia. Add a personal note: Cytogenetic analysis of blast cells in childhood acute lymphoblastic leukemia has led to the recognition of specific non-random chromosomal abnormalities with prognostic value.

Alteraciones cromosómicas en la leucemia linfoblástica aguda – ScienceDirect

Check out this article to learn more or contact your system administrator. Houston, we have a problem! Isolation and characterization of the gene responsible for the X chromosome- linked Kallmann syndrome. Case report and review. The incidence of chromosome anomalies in newborn infants is 0. The use of telomere probes to investigate submicroscopic rearrangements associated with mental retardation.


Prenat Diagn, 13pp.

Repercusión clínica de las anomalías cromosómicas | Anales de Pediatría

Send the ano,alias below via email or IM. Analysis of an interstitial deletion in a patient with Kallmann syndrome, X-linked ichthyosis and mental retardation.

Detection of break ano,alias in submicroscopic chromosomal translocation, illustrating an important mechanism for genetic disease. More presentations by valentina vasquez Propuesta de desarrollo de un acuario au Neither you, nor the coeditors you shared it with will be able to recover it again. By continuing you agree to the use of cookies.

Two cases of Robertsonian translocations in oligozoospermic males and their consequences for pregnancies induced by intracytoplasmatic sperm injection.

Most patients with ALL show karyotype abnormalities, either in chromosome number ploidy or as structural changes such as translocations, inversions, or deletions. Cytogenet Cell Genet, 41pp. A firewall is blocking access to Prezi content. Si continua navegando, consideramos que acepta su uso. Do you ccromosomicas want to delete this prezi?

Citogenética Clínica

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Ctomosomicas Genet, 34pp. Send link to edit together this prezi using Prezi Meeting learn more: Chromosomal rearrangements in three infertile men.

De ano,alias balanced chromosome rearrangement and extra marker chromosomes identified at prenatal diagnosis: Hum Genet, 82pp. You can change the settings or obtain more information by clicking here. Reset share links Resets both viewing and editing links coeditors shown below are not affected.

Prenat Diagn, 11pp. Houston, we have a problem! A firewall is blocking access to Prezi content. Molecular cytogenetic study of supernumerary marker chromosomes in an unselected group of children.

Am J Med Genet, 61pp. Please log in to add your comment. Pediatr Pathol, 10pp. El material extra interfiere con el desarrollo normal. The phenotypic manifestations of chromosomal abnormalities are highly diverse. Present to your audience.