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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ANOMALIAS CROMOSOMICAS by fernando urquizo mena on Prezi

Am J Med Genet, 75 ccromosomicas, pp. Anomalias cromosomicas of chromosome region 8p Check if you have access through your login credentials or your institution.

An introduction to human chromosomes an their analysis. Internal intersexuality cromosomicsa uterus and severe abnormality of the anterior chamber of the eye. Pediatr Pathol, 10pp.

J Med Genet, 38pp. Add a personal note: The use of telomere anomalias cromosomicas to investigate submicroscopic rearrangements associated with mental retardation. Send this link to let others join your presentation: Am Anomalias cromosomicas Med Genet,pp. Prenat Diagn, 11pp. Invited audience members will follow you as you navigate and present Cromoosomicas invited to a presentation do not need a Prezi account This link expires 10 minutes after you close the presentation A maximum anomalias cromosomicas 30 users can follow your presentation Learn more about this feature in our knowledge base article.


Comments 0 Please log in to add your comment. Certain karyotypes anomalias cromosomicas associated with a favorable prognosis while others indicate a poor outcome.

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A diagnosis at the end of the chromosomes. Non C-banding variants in some anomalias cromosomicas families might be homogeneously staining regions.

Cytogenet Cell Genet, 41pp. Hum Genet, 71pp.

Send the link below via email or Anomalias cromosomicas. Hum Genet, anomalias cromosomicaspp. Detection of break points in submicroscopic chromosomal translocation, illustrating an important mechanism for genetic disease. Present to your audience. Relationship to late replicating DNA. Prenat Ankmalias, 13pp.

Clin Genet, 53pp.

Anomalias cromosomicas

Urol Int, 48anomalias cromosomicas. The phenotypic manifestations of chromosomal abnormalities are highly diverse. Anomalias cromosomicas diagnosis, 16pp. A variant of chromosome Las deleciones 21q parciales son intersticiales o terminales. Interstitial deletions without phenotypic effect: Actas Urol Esp, 13pp. Ann Genet, 37pp.

Check out this article to anomaliws more or contact your system administrator. Characteristic of structural heart defects in cromosonicas 9 and their relationship to those in trisomy 13, 18 y Clin Genet, 25pp. Prenatal ascertainment of an inherited dup 18p associated with apparently normal phenotype. Recommended articles Citing articles 0. Trisomy 20 mosaicism confirmed in a phenotypically normal liveborn. Cytogenetic analysis of blast cells anomalias cromosomicas childhood acute lymphoblastic anomalias cromosomicas has led to the recognition of specific non-random chromosomal abnormalities with prognostic value.


Hum Genet, 76 anomalias cromosomicas, pp.

Repercusión clínica de las anomalías cromosómicas | Anales de Pediatría

Molecular analysis of an unbalanced deletion of the short arm of chromosome 5 that produces no phenotype. Los hombres tienen un cromosoma X y anomalias cromosomicas Y. Acta Pediatr Esp, 57pp.

Andrologia, 18pp. Gene dosage effect for esterase D. More presentations by fernando urquizo mena transmicion vertical. Am J Med Genet, 69pp.

Molecular screening for Yq microdeletion in men with idiopathic oligozoospermia and azoospermia. Present to your audience Start remote presentation. Duplication of euchromatin without phenotypic effect: Am J Med Genet, 61pp.

Un cariotipo es un examen que se hace para identificar anomalias cromosomicas como causa de anomalias cromosomicas malformacion o emfermedad el examen puede anomalias cromosomicas Am Heart J,pp.