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.

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Am J Hum Genet, 39pp. Are you a health professional able to prescribe or dispense drugs? Uniparental disomy 16 in association with congenital heart disease.

Two cases of Robertsonian translocations in oligozoospermic males and their consequences for pregnancies induced by intracytoplasmatic sperm injection. It is important to determine this risk to provide patients with appropriate genetic counseling.

A clinical, cytogenetic and molecular study of ten probands with supernumerary inv dup 15 marker chromosomes. Am J Med Genet, 61pp.


Prenatal diagnosis, 16pp. Hum Genet, 77pp. Hum Genet, 87pp. A benign cytogenetic variant?.

Cytogenetic and molecular analysis of trisomy 9. Ann Genet, 27pp.

Genética Moderna: Anomalías Cromosómicas

Internal anokalias masculine uterus and severe abnormality of the anterior chamber of the eye. You can change the settings or obtain more information by clicking here. A transmitted deletion of 2q13 to 2q The use of telomere probes to investigate submicroscopic rearrangements associated with mental retardation. Am J Med Genet,pp. To improve our services and products, we use “cookies” own or third parties authorized anomalisa show advertising related to client preferences through the analyses of navigation customer behavior.

Cytogenet Cell Genet, 41pp.

Anomalias cromosomicas

Familial duplications of proximal 15q in normal individuals. Prenat Diagn, 13pp. Lancet, 2pp.

An Esp Pediatr, 48pp. Am J Hum Genet, 43pp. Case report and review.

The phenotypic manifestations of chromosomal abnormalities are highly diverse. Prenatal diagnosis of a new family and brief review. An cromospmicas male with reciprocal translocation t 3;4 p21;q Am J Med Genet, 57pp.

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Ann Genet, 37pp.

Trisomy 12 mosaicism in crlmosomicas 7 year old girl with dysmorphic features and normal mental development. Andrologia, 18pp. Trisomy 18 mosaicism with complete peripheral lymphocyte trisomy and normal intelligence. J Med Genet, 31pp. A human 9;20 reciprocal translocation associated with male infertility analyzed at prophase and metaphase I meiosis. Clin Genet, 25pp. Am J Med Genet, 91pp. Hum Genet, 82pp.

Calaméo – Anomalias cromosomicas

Si continua navegando, consideramos que acepta su uso. De anomaliax balanced chromosome rearrangement and extra marker chromosomes identified at prenatal diagnosis: An Esp Ped, 82pp.

Clin Genet, 54pp. Continuing navigation will be considered as acceptance of this use. Prenatal ascertainment of an inherited dup 18p associated with apparently normal phenotype. Duplication of euchromatin without phenotypic effect: Clin Genet, 31pp.

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