ANOMALIAS CROMOSOMICAS PDF

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.

Clin Genet, 41pp. Am J Med Genet, 76pp. Clin Genet, 31pp. A transmitted deletion of 2q13 to 2q Cytogenetic and molecular analysis of trisomy 9. Acta Pediatr Esp, 57pp. The phenotypic manifestations of chromosomal abnormalities are highly diverse. J Med Genet, 38pp. Balanced reciprocal translocation mosaicism: Isolation and characterization of the gene responsible for the X chromosome- linked Kallmann syndrome. Molecular screening for Yq microdeletion in men with idiopathic oligozoospermia and azoospermia.

Clin Genet, 53pp.

Robertsonian translocation associated with azoospermia. Non C-banding variants in some normal families might be homogeneously staining regions. Gene dosage effect for esterase D. Prenatal diagnosis of a new family and brief review. Hum Genet, 96pp. Chromosomal rearrangements in three infertile men.

Lancet, 2pp. Am J Hum Genet, 43pp. An Esp Pediatr, 48pp. Internal intersexuality masculine uterus and severe abnormality of the anterior chamber of the eye. Am J Med Genet, 69pp. Hum Genet, 71pp. A variant of chromosome 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.

Urol Int, 44pp. Clinical significance and distribution of break points. Am J Med Genet,pp. Am J Med Genet, 61pp. Interstitial deletions without phenotypic effect: Hum Genet, 80pp. J Med Genet, 40pp.

Am J Med Genet, 36pp. Duplication of chromosome region 8p Hum Genet, 87pp.

Biomed Pharmacother, 48pp. You can change the settings or obtain more information by clicking here.

Anomalias cromosomicas

Am J Med Genet, 37pp. A benign cytogenetic variant?.

Uniparental disomy 16 in association with congenital heart disease. Andrologia, 18pp. Hospital 12 de Octubre.

Calaméo – Anomalias cromosomicas

The use of telomere probes to investigate submicroscopic rearrangements associated with mental retardation. Curr Opin Genet Dev, 13pp. A rare inherited euchromatic heteromorphism on chromosome 1. Chromosome imbalance, normal phenotype, and imprinting. Prenat Diagn, 9pp.

J Med Genet, 31pp. Am J Hum Genet, 49pp. Are you a health professional able to prescribe or dispense drugs? A clinical, cytogenetic and molecular crkmosomicas of ten probands with supernumerary inv dup 15 marker chromosomes.

Deletion of band 13q21 is compatible with normal phenotype. Clin Genet, 54pp. Ann Genet, 34pp.