Last Posted: Dec 19, 2019
- Absence of heterozygosity detected by single-nucleotide polymorphism array in prenatal diagnosis.
Liu Jialiu et al. Ultrasound in obstetrics & gynecology : the official journal of the International Society of Ultrasound in Obstetrics and Gynecology 2019 Dec - Outcomes of 4 years of molecular genetic diagnosis on a panel of genes involved in premature aging syndromes, including laminopathies and related disorders.
Grelet Maude et al. Orphanet journal of rare diseases 2019 Dec 14(1) 288 - The genetic workup for structural congenital heart disease.
Jerves Teodoro et al. American journal of medical genetics. Part C, Seminars in medical genetics 2019 Dec - Alternative option labeling impacts decision-making in noninvasive prenatal screening.
Fisher Camille F et al. Journal of genetic counseling 2019 Dec - Clinical utility of targeted gene enrichment and sequencing technique in the diagnosis of adult hereditary spherocytosis.
Xue Jun et al. Annals of translational medicine 2019 Oct 7(20) 527 - Culturally Targeted Video Improves Psychosocial Outcomes in Latina Women at Risk of Hereditary Breast and Ovarian Cancer.
Hurtado-de-Mendoza Alejandra et al. International journal of environmental research and public health 2019 Nov 16(23) - Effectiveness of the Genomics ADvISER decision aid for the selection of secondary findings from genomic sequencing: a randomized clinical trial.
Bombard Yvonne et al. Genetics in medicine : official journal of the American College of Medical Genetics 2019 Dec - Information Women Choose to Receive About Prenatal Chromosomal Microarray Analysis.
Hochner Hagit et al. Obstetrics and gynecology 2019 Dec - It takes two: uptake of carrier screening among male reproductive partners.
Giles Choates Meagan et al. Prenatal diagnosis 2019 Dec - Low Rates of Genetic Counseling and Testing in Individuals at Risk for Lynch Syndrome reported in the National Health Interview Survey.
Faust Nolan et al. Gastroenterology 2019 Dec
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