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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Repercusión clínica de las anomalías cromosómicas | Anales de Pediatría

Hum Genet, 71pp. Detection of break points in submicroscopic chromosomal translocation, illustrating an important mechanism for genetic disease. Clinical significance and distribution of break points. Analysis of an interstitial deletion in a patient with Kallmann syndrome, X-linked ichthyosis and mental retardation.

Anomalias Cromosomicas by valentina vasquez on Prezi

Am J Med Genet, 56pp. Si continua navegando, consideramos que acepta su uso.


Molecular cytogenetic study of supernumerary marker chromosomes in an unselected group of children. Isolation and characterization of the gene responsible for the X chromosome- linked Kallmann syndrome. Hum Genet, 59pp. Hum Genet, 82pp. Hum Cromosomicxs, 96pp.

An Esp Ped, 82pp. Proximal 15q variant with normal phenotype in three unrelated individuals. Prenatal diagnosis, 16pp. Molecular analysis of an unbalanced deletion of anomaliaw short arm of chromosome 5 that produces no phenotype.

Urol Int, 48pp. Ann Genet, 37pp. Trisomy 18 mosaicism with complete peripheral lymphocyte trisomy and normal intelligence.

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Chromosome imbalance, normal phenotype, and imprinting. Clin Genet, 41pp. Prenat Diagn, 13pp. Hum Genet, 70pp. First report in North America, 37anomaliaas.

Anomalias cromosomicas

Hum Reprod, 12pp. Two cases of Robertsonian translocations in oligozoospermic males and their consequences for pregnancies induced by intracytoplasmatic sperm injection.

Hum Genet, 77pp. Am J Hum Genet, 43pp. Am J Med Genet, 36pp. Continuing crkmosomicas will be considered as acceptance of this use.


Am J Med Genet, 37pp. J Med Genet, 27pp. An Esp Pediatr, 49pp. Am J Med Genet, 69pp.

A benign cytogenetic variant?. Familial duplications of proximal 15q in normal individuals.

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