The development of genotyping and sequencing techniques has been dramatic during the recent years. Now it is possible to obtain a full view over an individual’ s genetic landscape in the form of a million common single-nucleotide polymorphisms (SNPs) in single and affordable experiments. When you are citing the document, use the following link http://essuir.sumdu.edu.ua/handle/123456789/3230
Prenatal diagnosis of hereditary diseases has substantially altered the way medical geneticists are ...
Plasma DNA obtained from a pregnant woman contains a mixture of maternal and fetal DNA. The fetal DN...
Background Screening tests for Trisomy 21 (T21), also known as Down syndrome, are routinely perfo...
The development of genotyping and sequencing techniques has been dramatic during the recent years. N...
The analysis of cell-free fetal nucleic acids in maternal blood for prenatal diagnosis has been tran...
Prediction of fetal DNA allows diagnosing known/passed mutations before child’s birth. Public health...
Prediction of fetal DNA allows diagnosing known/passed mutations before child’s birth. Public health...
Prenatal diagnosis involves all available procedures to determine the health status of a fetus or em...
BACKGROUND: Plasma DNA obtained from a pregnant woman contains a mixture of maternal and fetal DNA. ...
Motivation: A growing body of literature has demonstrated the potential for non-invasive diagnosis o...
Motivation: Numerous genetic disorders can be detected in prenatal diagnosis using Chorionic Villus ...
Genome-wide linkage analysis is an established tool to map inherited diseases. To our knowledge it h...
PURPOSE: Whereas noninvasive prenatal screening for aneuploidies is widely implemented, there is an ...
screening for Mendelian disorders may be clinically feasible in the near future. methods must be ref...
<div><h3>Background</h3><p>Plasma DNA obtained from a pregnant woman contains a mixture of maternal ...
Prenatal diagnosis of hereditary diseases has substantially altered the way medical geneticists are ...
Plasma DNA obtained from a pregnant woman contains a mixture of maternal and fetal DNA. The fetal DN...
Background Screening tests for Trisomy 21 (T21), also known as Down syndrome, are routinely perfo...
The development of genotyping and sequencing techniques has been dramatic during the recent years. N...
The analysis of cell-free fetal nucleic acids in maternal blood for prenatal diagnosis has been tran...
Prediction of fetal DNA allows diagnosing known/passed mutations before child’s birth. Public health...
Prediction of fetal DNA allows diagnosing known/passed mutations before child’s birth. Public health...
Prenatal diagnosis involves all available procedures to determine the health status of a fetus or em...
BACKGROUND: Plasma DNA obtained from a pregnant woman contains a mixture of maternal and fetal DNA. ...
Motivation: A growing body of literature has demonstrated the potential for non-invasive diagnosis o...
Motivation: Numerous genetic disorders can be detected in prenatal diagnosis using Chorionic Villus ...
Genome-wide linkage analysis is an established tool to map inherited diseases. To our knowledge it h...
PURPOSE: Whereas noninvasive prenatal screening for aneuploidies is widely implemented, there is an ...
screening for Mendelian disorders may be clinically feasible in the near future. methods must be ref...
<div><h3>Background</h3><p>Plasma DNA obtained from a pregnant woman contains a mixture of maternal ...
Prenatal diagnosis of hereditary diseases has substantially altered the way medical geneticists are ...
Plasma DNA obtained from a pregnant woman contains a mixture of maternal and fetal DNA. The fetal DN...
Background Screening tests for Trisomy 21 (T21), also known as Down syndrome, are routinely perfo...