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Prenatal diagnosis of a chromosome abnormality is only possible currently through two procedures: Chorionic Villus Sampling (CVS) and Amniocentesis. Both procedures are capable of diagnosing chromosome abnormalities, however they differ in several key ways including timing during the pregnancy and the type of specimen used to make the diagnosis. To find out which is most appropriate for you, please contact your primary care doctor or obstetrician.
To make a definitive diagnosis, the child's X chromosome is analyzed for defects in the Btk gene. Similar analysis can be used for prenatal diagnosis or to detect carriers of the defective gene
To make a definitive diagnosis, the child's X chromosome is analyzed for defects in the Btk gene. Similar analysis can be used for prenatal diagnosis or to detect carriers of the defective gene
To make a definitive diagnosis, the child's X chromosome is analyzed for defects in the Btk gene. Similar analysis can be used for prenatal diagnosis or to detect carriers of the defective gene
Aliza Kolker has written: 'Prenatal testing' -- subject- s -: Genetic counseling, Prenatal diagnosis, Psychological aspects, Psychological aspects of Genetic counseling, Psychological aspects of Prenatal diagnosis, Social aspects, Social aspects of Genetic counseling, Social aspects of Prenatal diagnosis
It is a prenatal test that can detect genetic and chromosomal abnormalities of an unborn baby
It is a prenatal test that can detect genetic and chromosomal abnormalities of an unborn baby
Not at the current time.
John L. Hamerton has written: 'Highlights from Prenatal diagnosis in Canada, 1990' -- subject(s): Diagnosis, Diseases, Fetus, Human reproductive technology, Obstetrics, Prenatal diagnosis
It is a prenatal test that can detect genetic and chromosomal abnormalities of an unborn baby
Amniocentesis and chorionic villi sampling.
Ultrasound, amniocentesis or chorionic villi sampling checks for chromosomal abnormalities in the fetus.