Results 271 to 280 of about 1,654,437 (300)
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Preimplantation genetic diagnosis
Current Opinion in Pediatrics, 1994Preimplantation genetic diagnosis now represents an alternative reproductive option for parents at high risk of having offspring affected with certain genetic diseases. Progress in the past year has included increasing reliability in embryo sexing by both polymerase chain reaction and fluorescent in situ hybridization techniques; delivery of babies ...
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Pediatrics In Review, 1980
The fundamental philosophy of prenatal genetic diagnosis is to enable prospective parents at risk to have children selectively, unaffected by a specific hereditary disorder.1 In practice, this new technology has allowed healthy children to be born to many couples who, without the reassurance that it is now possible to extend to them, would not have had
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The fundamental philosophy of prenatal genetic diagnosis is to enable prospective parents at risk to have children selectively, unaffected by a specific hereditary disorder.1 In practice, this new technology has allowed healthy children to be born to many couples who, without the reassurance that it is now possible to extend to them, would not have had
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Genetic Programming in Medical Diagnosis
2003The paper describes the results obtained for differential diagnostics of substantially complex disorders in the acid-base status. Since the first attempts of applying the genetic programming to this problem, presented by the authors at MIE 2000, proved promising, the investigation has been continued.
Andrzej Malolepszy, Edward Kacki
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Genetic Aspects of Prenatal Diagnosis
Journal of Inherited Metabolic Disease, 1989SummaryWith improved control of environmental agents, genetic conditions are now a major cause of residual handicap and mortality in all age groups. Primary prevention of this diverse group of over 5000 distinct disorders is not yet possible and effective therapy is, as yet, available for very few.
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Prenatal Diagnosis of Genetic Disorders
New England Journal of Medicine, 1976Each year in the United States alone, there are more than 20,000 live births with chromosomal abnormalities.1 We estimate that in 1973, chromosomal abnormalities were diagnosed in fewer than 75 fetuses in utero. There would appear to be three major reasons to explain this remarkably small number of intrauterine genetic diagnoses made in one year: (1 ...
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Genetic testing in prostate cancer management: Considerations informing primary care
Ca-A Cancer Journal for Clinicians, 2022Veda N Giri, Todd M Morgan, David Morris
exaly
New developments in the diagnosis and treatment of thyroid cancer
Ca-A Cancer Journal for Clinicians, 2013David F Schneider, Herbert Chen
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Recent progress in the diagnosis and treatment of ovarian cancer
Ca-A Cancer Journal for Clinicians, 2011Deborah Armstrong
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Hydatidiform Moles: Genetic Basis and Precision Diagnosis
Annual Review of Pathology: Mechanisms of Disease, 2017Pei Hui, Natalia Buza
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