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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Hum Genet, 82pp. More presentations by valentina vasquez Propuesta de desarrollo de un acuario au Check out this article to learn more or contact your system administrator. Hum Genet, 77pp.

Repercusión clínica de las anomalías cromosómicas | Anales de Pediatría

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An Esp Ped, 82pp. Creating downloadable prezi, be patient. Prenat Diagn, 13pp.

Internal intersexuality masculine uterus and severe abnormality of the anterior chamber of the eye. Trisomy 20 mosaicism confirmed in a phenotypically normal liveborn. See more popular or the latest prezis. Are you a health professional able to prescribe or dispense drugs? Add a personal note: A diagnosis at the end of the chromosomes.

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Hum Genet, 87pp. Cancel Reply 0 characters used crimosomicas the allowed. Analysis of an interstitial deletion in a patient with Kallmann syndrome, X-linked ichthyosis and mental retardation.

Recommended articles Citing articles 0. Am Heart J,pp. Am J Med Genet, 56pp. El material extra interfiere con el desarrollo normal.

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Cytogenet Cell Genet, 41pp. You can change the settings or obtain more information by clicking here. A firewall is blocking access to Prezi content. Creating downloadable prezi, be patient.

Duplication of euchromatin without phenotypic effect: Trisomy 12 mosaicism in a 7 year old girl with dysmorphic features and normal mental development. Send the link below via email or IM Copy. Neither you, nor the coeditors you shared it with will be able to recover it again. Am Annomalias Hum Genet, 43pp.

Send the link below via email or IM. Do you really want to delete this prezi? It is important to determine this risk to provide patients with appropriate genetic counseling. Prenat Diagn, 9pp. Prenatal ascertainment of an inherited dup 18p associated with apparently normal phenotype. An Esp Pediatr, 49pp. Cytogenetic and molecular analysis of trisomy 9. An Esp Pediatr, 48pp. Delete comment or cancel. A human 9;20 reciprocal translocation associated with male infertility analyzed at prophase and metaphase I meiosis.


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Citogenética Clínica

Non C-banding variants in some normal families might be homogeneously staining regions. Trisomy 18 mosaicism with complete peripheral lymphocyte trisomy and normal intelligence. Familial duplications of proximal 15q in normal individuals.

Houston, we have a problem! Prenatal diagnosis of a new family and brief review. J Med Genet, 40pp.