Literature DB >> 8237909

Human cytogenetics. A current overview.

M M Cohen1, L S Rosenblum-Vos, G Prabhakar.   

Abstract

Chromosomal abnormalities are the basis for a substantial proportion of human morbidity and mortality. During the past 35 years, the field of human cytogenetics has helped to elucidate the etiology of many congenital malformation/mental retardation syndromes. Through adaptation of technological advances and integration of molecular biological techniques, cytogenetics continues to contribute significantly to our knowledge of clinical genetics, chromosomal fine structure and function, gene mapping, and prenatal diagnosis. This review outlines the basic concepts, recent findings, and current laboratory approaches to cytogenetic diagnosis.

Entities:  

Mesh:

Substances:

Year:  1993        PMID: 8237909     DOI: 10.1001/archpedi.1993.02160350033005

Source DB:  PubMed          Journal:  Am J Dis Child        ISSN: 0002-922X


  3 in total

1.  Use of nonbreakpoint DNA probes to detect the t(X;18) in interphase cells from synovial sarcoma: implications for detection of diagnostic tumor translocations.

Authors:  M Zilmer; C P Harris; D S Steiner; L F Meisner
Journal:  Am J Pathol       Date:  1998-05       Impact factor: 4.307

2.  De novo generation of simple sequence during gene amplification.

Authors:  L S Kirschner
Journal:  Nucleic Acids Res       Date:  1996-07-15       Impact factor: 16.971

3.  Screening of Fetal Chromosome Aneuploidies in the First and Second Trimester of 125,170 Iranian Pregnant Women.

Authors:  Elham Seyyed Kavoosi; Sarang Younessi; Dariush D Farhud
Journal:  Iran J Public Health       Date:  2015-06       Impact factor: 1.429

  3 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.