Congenital Malformations, Deformations and Chromosomal Abnormalities in Cyprus

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Association of Fetal and Parental Chromosomal Abnormalities with Congenital Anomalies

Background & Aims: Chromosome abnormalities are a major cause of miscarriage and neonatal mortality. The present study aimed to determine the association of fetal and parents chromosomal abnormalities with congenital anomalies. Methods: A cross-sectional study was performed in a tertiary referral center (Afzalipour Hospital) over 16 months period (2011-2012). The study groups consisted of 77 fe...

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Chromosomal abnormalities and congenital heart disease.

In this study the authors attempted to determine the frequency of the classical chromosomal syndromes as a cause of congenital heart disease and sought other cytogenetic abnormalities in patients with congenital heart disease, selected either for the presence of extracardiac abnormalities or the existence of congenital heart disease in other members of the family. Of the 275 patients whose kary...

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Chromosomal Abnormalities and Congenital Heart Disease

In this study the authors attempted to determine the frequency of the classical chromosomal syndromes as a cause of congenital heart disease and sought other cytogenetic abnormalities in patients with congenital heart disease, selected either for the presence of extracardiac abnormalities or the existence of congenital heart disease in other members of the family. Of the 275 patients whose kary...

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Chromosomal abnormality associated with congenital macroglossia and other abnormalities.

Armendares, S., Buentello, L., Salamanca, F., and Cantu-Garza, J. M. (1972). A dicentric Y chromosome without evidence of sex chromosomal mosaicism, 46,XYqdic, in a patient with features of Turner's syndrome. Journal of Medical Genetics, 9, 96-100. Caspersson, T., Lomakka, G., and Zech, L. (1971). The 24 fluorescence patterns of the human metaphase chromosomes-distinguishing characters and vari...

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Chromosomal Abnormalities in Patients with Congenital Heart Disease

BACKGROUND Chromosomal abnormalities (CAs) are an important cause of congenital heart disease (CHD). OBJECTIVE Determine the frequency, types and clinical characteristics of CAs identified in a sample of prospective and consecutive patients with CHD. METHOD Our sample consisted of patients with CHD evaluated during their first hospitalization in a cardiac intensive care unit of a pediatric ...

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ژورنال

عنوان ژورنال: The International Annals of Medicine

سال: 2018

ISSN: 2520-5110

DOI: 10.24087/iam.2018.2.7.567