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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Am Cromosomifas Med Cromosomicaz, 37pp. Trisomy 18 mosaicism with complete peripheral lymphocyte trisomy and normal intelligence. Molecular screening for Yq microdeletion in men with idiopathic oligozoospermia and azoospermia.
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Endocr Metab Clin North Am, 25pp. Am J Hum Genet, 39pp. Clin Genet, 53pp. A benign cytogenetic variant?. Andrologia, 18pp. Continuing navigation will be considered as acceptance of this use.
Calaméo – Anomalias cromosomicas
Prenatal diagnosis of a new family and brief review. It is important to determine this risk to provide patients with appropriate genetic counseling. Hum Genet, 71pp. Non C-banding variants in some normal families might be homogeneously staining regions.
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Relationship to late replicating DNA. Characteristic of structural heart defects in trisomy 9 and their relationship to those in trisomy 13, 18 y Lancet, 2pp.
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Report of two patinets, one with a trisomic sib due to a maternal insertion. Balanced reciprocal translocation mosaicism: Prenat Diagn, 9pp.
Risk of phenotypic abnormalities in paracentric inversion carriers. Clin Genet, 31pp. A diagnosis at the end of the chromosomes. Cromosomifas can change the settings or obtain more information by clicking here. Cytogenet Cell Genet, 41pp.
Am J Med Genet, 41pp. Cytogenetic and molecular analysis of inv dup 15 chromosomes observed in two patients with autistic disorder and mental retardation. Clin Genet, 25pp. Phenotypic consequences of chromosome abnormalities.
Hum Reprod, 12pp. Robertsonian translocation associated with azoospermia. Translocation t 1;5 q21;p13 in a male with azoospermia. Deletion of band 13q21 is compatible with normal phenotype. Pediatr Pathol, 10pp. Full mosaic monosomy 22 in a child with DiGeorge syndrome facial appearance. Familial duplications of proximal 15q in normal individuals.
An azoospermic male with reciprocal translocation t 3;4 p21;q Hum Genet, 96pp. Cromisomicas Diagn, 11pp. Prenatal ascertainment of an inherited dup 18p associated with apparently normal phenotype. A variant of chromosome Clinical significance and distribution of break points. Heritable deletion of band 16q21 with normal phenotype: Hum Genet, 76pp.
Molecular cytogenetic study of supernumerary marker chromosomes in an unselected group of children. Ann Genet, 34pp. Duplication of chromosome region 8p Si continua navegando, consideramos que acepta su uso.