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pro vyhledávání: '"Kathryn Steinhaus French"'
Autor:
Forum T. Shah, Kathryn Steinhaus French, Kathryn E. Osann, Maureen Bocian, Marilyn C. Jones, Lauren Korty
Publikováno v:
Journal of Clinical Medicine, Vol 3, Iss 3, Pp 849-864 (2014)
Until recently, maternal serum analyte levels paired with sonographic fetal nuchal translucency measurement was the most accurate prenatal screen available for Trisomies 18 and 21, (91% and 94% detection and false positive rates of 0.31% and 4.5% res
Externí odkaz:
https://doaj.org/article/9d6823874cf748be9127bbc5136d66c8
Publikováno v:
Journal of Genetic Counseling. 31:1238-1248
This focused revision builds on the expert opinions from the original publications of 'Recommendations for human standardized pedigree nomenclature' published in 1995 and updated in 2008. Our review of medical publications since 2008 did not identify
Publikováno v:
Journal of genetic counselingREFERENCES.
Autor:
Kathryn Osann, Kathryn Steinhaus French, Forum T. Shah, Maureen Bocian, Marilyn C. Jones, Lauren Korty
Publikováno v:
Journal of Clinical Medicine; Volume 3; Issue 3; Pages: 849-864
Journal of Clinical Medicine
Journal of Clinical Medicine, Vol 3, Iss 3, Pp 849-864 (2014)
Shah, FT; French, KS; Osann, KE; Bocian, M; Jones, MC; & Korty, L. (2014). Impact of Cell-Free Fetal DNA Screening on Patients' Choice of Invasive Procedures after a Positive California Prenatal Screen Result.. Journal of clinical medicine, 3(3), 849-864. doi: 10.3390/jcm3030849. UC Irvine: Retrieved from: http://www.escholarship.org/uc/item/3qf0j721
Journal of Clinical Medicine
Journal of Clinical Medicine, Vol 3, Iss 3, Pp 849-864 (2014)
Shah, FT; French, KS; Osann, KE; Bocian, M; Jones, MC; & Korty, L. (2014). Impact of Cell-Free Fetal DNA Screening on Patients' Choice of Invasive Procedures after a Positive California Prenatal Screen Result.. Journal of clinical medicine, 3(3), 849-864. doi: 10.3390/jcm3030849. UC Irvine: Retrieved from: http://www.escholarship.org/uc/item/3qf0j721
Until recently, maternal serum analyte levels paired with sonographic fetal nuchal translucency measurement was the most accurate prenatal screen available for Trisomies 18 and 21, (91% and 94% detection and false positive rates of 0.31% and 4.5% res
Publikováno v:
Journal of Genetic Counseling. 17:424-433
In 1995, the Pedigree Standardization Task Force (PSTF) of the National Society of Genetic Counselors (NSGC) proposed a system of pedigree nomenclature. Recently, the PSTF (now called the Pedigree Standardization Work Group or PSWG) sought evidence t