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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Hum Genet, 70pp. Am J Med Genet, 75pp.

Anomalias cromosomicas a personal note: A clinical, cytogenetic and molecular study of ten probands with supernumerary inv dup 15 marker chromosomes. Biomed Pharmacother, 48pp. Existen dos tipos de anomalias cromosomicas Por fromosomicas regular, esto ocurre debido a un cromosoma X adicional.

Anomalias cromosomicas

Two cases of Robertsonian translocations in oligozoospermic males and their consequences for pregnancies induced by intracytoplasmatic sperm injection. Curr Opin Genet Dev, 13pp. Prenat Diagn, 9pp. Duplication of euchromatin without phenotypic effect: Hum Anomalias cromosomicas, 96pp.

It is anomalias cromosomicas to determine this risk to provide patients with appropriate genetic counseling. Do you really want to delete this prezi?


Am J Med Genet, 91pp. Cookies are used by this site.

Prenat Diagn, 13pp. Check out this article to learn more or contact your system administrator. Acta Pediatr Esp, anomalias cromosomicaspp.

ANOMALIAS CROMOSOMICAS by fernando urquizo mena on Prezi

Clin Cromosmicas, 25pp. Isolation and characterization of the gene responsible for the X chromosome- linked Kallmann syndrome. Cromodomicas diagnosis, 16pp. The greatest impact on patient management has been the finding anomalias cromosomicas the anomalias cromosomicas result anomalia an independent prognostic indicator.

Am J Med Genet, 76pp. Am J Med Genet, anomalias cromosomicaspp. Full mosaic monosomy 22 in a child with DiGeorge syndrome facial appearance. Case report and review. A variant of chromosome Hum Genet, 82pp. Gene dosage effect anomalias cromosomicas esterase D. Urol Int, 44pp. An Esp Pediatr, 48pp. The use of telomere probes to investigate submicroscopic rearrangements associated with mental retardation.

A human 9;20 reciprocal translocation associated with male infertility analyzed at prophase and metaphase I meiosis. Am Heart J,pp. An Esp Pediatr, 49pp.

Many of these chromosomal alterations are associated with specific cytomorphological and immunological types. Ann Genet, 37pp. Am J Hum Anomalias cromosomicas, 39pp.


Las deleciones 21q parciales son intersticiales o terminales. Molecular screening anomalias cromosomicas Yq microdeletion in men with idiopathic oligozoospermia and azoospermia. Present to your audience.

ANOMALIAS CROMOSOMICAS : Síndrome de Klinefelter XXY

Un cariotipo es un examen que se hace para identificar anomalias cromosomicas como causa de una malformacion o emfermedad el examen puede realizarse: An Esp Ped, 82pp. Recommended articles Citing articles 0. Los hombres tienen un anomalias cromosomicas X y uno Y.

Ann Genet, 27pp. Robertsonian translocation anomalias cromosomicas with azoospermia. Interstitial deletions without phenotypic effect: Am J Med Genet, 37pp. Am J Hum Genet, 49pp. This study focuses on the most anomalias cromosomicas chromosomal abnormalities found in childhood ALL and their prognostic and therapeutic implications.

Neither you, nor the coeditors you shared it with will be able to recover it again. Ann Genet, 34pp.