ANOMALIAS DETECTADAS EN BOGOTÁ LOS ULTIMOS 10 AÑOS. SINDROME DE ANGELMAN. ¿QUE ANOMALIAS SE HAN DETECTADO. Biología y Genética – ro Fa ent C cu ro lín lt d ic ad e G a Al de en em M ét i e . Convert documents to beautiful publications and share them worldwide. Title: Anomalias cromosomicas, Author: Simon Bolivar, Length: 20 pages, Published.

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Curr Opin Genet Dev, 13 cromosomicss, pp. Are you a health professional able to prescribe or dispense drugs? Prenatal diagnosis, 16pp.

Hum Reprod, 12pp. Balanced reciprocal translocation mosaicism: Cytogenetic and molecular analysis of trisomy 9. Prenat Diagn, 11pp. An Esp Pediatr, 48pp.

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Molecular cytogenetic study of supernumerary marker chromosomes in an unselected group of children. Case report and review.

Repercusión clínica de las anomalías cromosómicas | Anales de Pediatría

A transmitted deletion of 2q13 to 2q 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. Ann Genet, 37pp. Characteristic of structural heart defects in trisomy 9 and their relationship to those in trisomy 13, 18 y An Esp Pediatr, 49pp. Am Heart J,pp. Two cases of Robertsonian translocations in oligozoospermic males and their consequences for pregnancies induced by intracytoplasmatic sperm injection.

Non C-banding variants in some normal families might be homogeneously staining regions. Analysis of an interstitial deletion in cromosomicaa patient with Kallmann syndrome, X-linked ichthyosis and mental retardation.

Hum Genet, 77 cromosomicsa, pp. Gene dosage effect for esterase D. Am J Hum Genet, 43pp. Continuing navigation will be considered as acceptance of this use. Interstitial deletions without phenotypic effect: J Biosci, 28pp. Hum Genet, 96pp.

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Results from a year incidence study in Arhus, Denmark. Clin Genet, 53pp. Chromosome imbalance, normal phenotype, and imprinting.

Anomalias cromosomicas

Hum Genet, 80pp. Heritable deletion of band 16q21 with normal phenotype: An introduction to human chromosomes an their analysis. Lancet, 2pp. Hum Genet, 59pp. Am J Med Genet, 91pp.

Robertsonian translocation associated with crokosomicas. Clinical significance and distribution of break points. Hum Genet, 82pp. The incidence of chromosome anomalies in newborn infants is 0. A variant of chromosome