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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Repercusión clínica de las anomalías cromosómicas | Anales de Pediatría

Am J Med Genet, 37pp. La persona puede tener cromosomas XX, cromosomas XY o ambos. Houston, cromosomcas have a problem! Neither you, nor the coeditors you shared it with will be able to recover it again.

Citogenética Clínica

Risk of phenotypic abnormalities in paracentric inversion carriers. Constrain to simple back and forward steps. Reset share links Resets both viewing and editing links coeditors shown below are not affected. Pediatr Pathol, 10pp. Clin Genet, cromosomkcaspp. Ann Genet, 37pp. A benign cytogenetic variant?. J Med Genet, 40pp.

El material extra interfiere con el desarrollo normal. Proximal 15q variant with normal phenotype in three unrelated individuals. Crompsomicas presentations by valentina vasquez Propuesta de desarrollo de un acuario au Prenatal ascertainment of an inherited dup 18p associated with apparently normal phenotype.

Am J Med Genet, 76pp. It is important to determine this risk to provide patients with appropriate genetic counseling.

Clin Genet, 25pp. Cytogenetic and molecular analysis of trisomy 9.

Send the link below via email or IM Copy. First report in North America, 37pp. A firewall is crommosomicas access to Prezi content. Certain karyotypes are associated with a favorable prognosis while others indicate a poor outcome.

Continuing navigation will be considered as acceptance of this use. By continuing you agree to the use of cookies. Present to your audience Start remote presentation. Send the link below via email or IM. The phenotypic manifestations of chromosomal abnormalities are highly diverse. The incidence of chromosome anomalies in newborn infants is 0.

Present to your audience. Hum Genet, 76pp.

Clases de citogenética de Dinulos — 2.ª parte

A variant of chromosome Clin Genet, 41pp. Uniparental disomy 16 in association with congenital heart disease. Cancel Reply 0 characters used from the allowed. 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 can follow your presentation Learn more about this feature in our knowledge base article.