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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Molecular cytogenetic study of supernumerary marker chromosomes in an unselected group of children. A diagnosis at the end of the chromosomes.

Citogenética Clínica

Urol Int, 48pp. A transmitted deletion of 2q13 to 2q It is important to determine this risk to provide patients with appropriate genetic counseling. Delete comment or cancel. An Esp Pediatr, 48pp. Cromosomicaa J Med Genet, 76pp.


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Do you really want to delete this prezi? A clinical, cytogenetic and molecular study of ten probands with supernumerary inv dup 15 marker chromosomes.

Chromosome imbalance, normal phenotype, and imprinting. Cytogenetic analysis of blast cells in childhood acute lymphoblastic leukemia has led to the recognition of specific non-random chromosomal abnormalities with prognostic value. El material extra interfiere con el desarrollo normal. Cytogenetic and molecular analysis of inv dup 15 chromosomes observed in two patients with autistic disorder and mental retardation. J Biosci, 28pp.

Anomalias Cromosomicas by valentina vasquez on Prezi

You can change the settings or obtain more information by clicking here. Hum Genet, 80pp. Actas Urol Esp, 13pp.

The phenotypic manifestations of chromosomal abnormalities are highly diverse. Send this link to let others join your presentation: Ann Genet, 27pp.


Chromosomal rearrangements in three infertile men. Andrologia, 18pp. Send the link below via email or IM Copy.

Repercusión clínica de las anomalías cromosómicas | Anales de Pediatría

Am J Hum Genet, 49pp. Clin Genet, 53pp. Translocation t 1;5 q21;p13 in a male with azoospermia. Hum Genet, 82pp. Check out this article to learn more or contact your system administrator.

Cancel Reply 0 characters used from the allowed. Balanced reciprocal translocation mosaicism: An azoospermic male with reciprocal translocation t 1;15 q11;p Heritable deletion of band 16q21 with normal phenotype: Am J Med Genet, 69pp. Interstitial deletions without phenotypic effect: