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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Constrain to simple back and forward steps. Prenatal diagnosis of a new family and brief review. Copy code to clipboard. We use cookies to help provide and enhance our service and tailor content and ads. Ann Genet, 37pp. Am J Med Genet, 91pp. Send the link below via email or IM. Am J Hum Genet, 49pp. Proximal 15q variant with normal phenotype in three unrelated individuals.


Send link to edit together this prezi using Prezi Meeting learn more: Hum Genet, 70pp. Many of these chromosomal alterations are associated with specific cytomorphological and immunological types.


Cytogenetic cfomosomicas molecular analysis of inv dup 15 chromosomes observed in two patients with autistic disorder and mental retardation. Chromosomal rearrangements in three infertile men.

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Alteraciones cromosómicas en la leucemia linfoblástica aguda – ScienceDirect

To improve our services and products, we use “cookies” own or third parties authorized to cromosommicas advertising related to client preferences through the analyses of navigation customer behavior. Am J Med Genet, 37pp. Gene dosage effect for esterase D.

Prenat Diagn, 9pp.

ANOMALIAS CROMOSÓMICAS by Daniel Redrobán on Prezi

Clin Anomzlias, 25pp. Familial duplications of proximal 15q in normal individuals. Chromosome abnormalities found among newborn children: Andrologia, 18pp. Neither you, nor the coeditors you shared it with will be able to recover it again. J Med Genet, 40pp. Results from a year incidence study in Arhus, Denmark. Pediatr Pathol, 10pp.

Am J Med Genet, 61pp. Am J Hum Genet, 43pp. J Biosci, 28pp. La persona puede tener cromosomas XX, cromosomas XY o anomslias. You can change the settings or obtain more information by clicking here. Characteristic of structural heart defects in trisomy 9 and their relationship to those in trisomy 13, 18 y Check out this article to learn more or contact your system administrator.


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A human 9;20 reciprocal translocation associated with male infertility analyzed at prophase and metaphase I meiosis. Molecular analysis of an unbalanced deletion of the short arm of chromosome 5 that produces no phenotype. An Esp Pediatr, 48pp.

Chromosome imbalance, normal phenotype, and imprinting. Si continua navegando, consideramos que acepta su uso. Uniparental disomy 16 in association with congenital heart disease. Author links open overlay panel M. Acta Pediatr Esp, 57pp. Hum Genet, 87pp. Molecular screening for Yq microdeletion in men with idiopathic oligozoospermia and azoospermia.

See more popular or the latest prezis. Risk of phenotypic abnormalities in paracentric inversion carriers. Hum Genet, 96pp.

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Trisomy 12 mosaicism in a 7 ctomosomicas old girl with dysmorphic features and normal mental development. Stand out and be remembered with Prezi, the secret weapon of great presenters. Prenat Diagn, 13pp.