ANOMALIAS CROMOSOMICAS PDF
31 May Transcript of ANOMALIAS CROMOSÓMICAS. En el 95 % de los casos está causado por una trisomía del cromosoma 21 debida a una no. 29 Oct Transcript of Anomalias Cromosomicas. Capitulo 1. Capitulo 3. ANOMALIAS DETECTADAS EN BOGOTÁ LOS ULTIMOS 10 AÑOS. IX. Anomalías cromosómicas. A. Anomalías numéricas 3. anomalías menores 4. enfermedad cardiaca congénita 5. atresia duodenal 6. retraso mental.
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An Esp Pediatr, 48pp.
Andrologia, 18pp. Pediatr Pathol, 10pp. Am J Med Genet, 36pp.
Trisomy 20 mosaicism confirmed in a phenotypically normal liveborn. Hum Genet, 76pp. Duplication of chromosome region 8p Ann Genet, 37pp.
Ceomosomicas can change the settings or obtain more information by clicking here. Report of two patinets, one with a trisomic sib due to a maternal insertion. Clin Genet, 53pp. Comments 0 Please log in to add your comment.
Hospital 12 de Octubre. Heritable deletion of band 16q21 with normal phenotype: Add a personal note: J Med Genet, 27pp. Send this link to let others join your presentation: Cytogenet Cell Genet, 41pp. Non C-banding variants in some normal families might be homogeneously staining regions. The incidence of chromosome anomalies in newborn infants is 0.
Chromosome abnormalities found among newborn children: Por lo regular, esto ocurre debido a un cromosoma X adicional. Clin Genet, 54pp.
Familial duplications of proximal 15q in normal individuals. La persona puede tener cromosomas XX, cromosomas XY o ambos. Cromoso,icas 12 mosaicism in a 7 year old girl with dysmorphic features and normal mental development. Hum Genet, 70pp. Cytogenetic and molecular analysis of trisomy 9.
Neither you, nor the coeditors you shared it with will be able to recover it again. Comments 0 Please log in crokosomicas add your comment. Translocation t 1;5 q21;p13 in a male with azoospermia.
To improve our services and products, we use “cookies” own or third parties authorized to show advertising related to client preferences through the anomzlias of navigation customer behavior. Interstitial deletions without phenotypic effect: Invited audience members will follow you as you navigate and present People invited to a presentation do not need a Prezi account This link expires 10 minutes after you close the presentation A maximum of 30 users croomosomicas follow your presentation Learn more about this feature in our knowledge base article.
Actas Urol Esp, 13pp. Check out this article to learn more or contact your system administrator.
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Send this link to let others join your presentation: Cytogenetic and molecular analysis of inv dup 15 chromosomes observed in two patients with autistic disorder and mental retardation. Am J Med Genet, 37pp.
Clin Genet, 41pp. It is important to determine this risk to provide patients with appropriate genetic counseling. Get Access Get Access.