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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Continuing navigation will be considered as acceptance of this use. First report in North America, 37pp. Am J Med Genet, 91pp. Case report and review. Duplication of chromosome region cro,osomicas Hum Genet, 96pp.

Clin Genet, 31pp. Prenat Diagn, 11pp. Molecular screening for Yq microdeletion in men with idiopathic oligozoospermia and azoospermia. Clin Genet, 25pp. Proximal cromsomicas variant with normal phenotype in three unrelated individuals. Deletion of band 13q21 is compatible with normal phenotype. Am Heart J,pp. J Med Genet, 38pp.


Anomalias cromosomicas

Urol Int, 44pp. An Esp Pediatr, 48pp. J Med Genet, 40pp.

Prenatal diagnosis, 16pp. Endocr Metab Clin North Am, 25pp. Cytogenetic and molecular analysis of trisomy 9. Molecular cytogenetic ceomosomicas of supernumerary marker chromosomes in an unselected group of children. Balanced reciprocal translocation mosaicism: Analysis of an interstitial deletion in a patient with Kallmann syndrome, X-linked ichthyosis and mental retardation.

J Med Genet, 27pp. 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.

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Familial duplications of proximal 15q in normal individuals. Trisomy 18 mosaicism with complete peripheral lymphocyte trisomy and normal intelligence. A benign cytogenetic variant?. Clin Genet, 41pp. You can change the settings or obtain more information by clicking here. Am J Med Genet, 41pp.

Trisomy 20 mosaicism confirmed in a phenotypically normal liveborn. Molecular analysis of an unbalanced deletion of the short arm of chromosome 5 that produces no phenotype. Report of two patinets, one with a trisomic sib due to a maternal insertion. Two cases of Robertsonian translocations in oligozoospermic males and their consequences for pregnancies induced by intracytoplasmatic sperm injection.

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Duplication of euchromatin without phenotypic effect: Hum Genet, 76pp. Prenatal ascertainment of an inherited dup 18p associated with apparently normal phenotype. Robertsonian translocation associated with azoospermia. Am J Med Genet, 61pp. Prenat Diagn, 9pp. Hum Genet, 77pp. Biomed Pharmacother, anomaliqspp. Andrologia, 18pp.