Zobrazeno 1 - 10
of 97
pro vyhledávání: '"J, Harraway"'
Autor:
B. Hutchinson, J Harraway, E Kluckow, Mark D. Pertile, Ricardo Palma-Dias, A Poulton, Debbie Nisbet, Anthea Lindquist, Melody Menezes, R. McCoy, Jane Halliday, Zeffie Poulakis, L. Bonacquisto, A Howden, Nicole Martin, L. Gugasyan, A Kulkarni, Lisa Hui, F. da Silva Costa, Michael T. Bethune
Publikováno v:
Ultrasound in Obstetrics & Gynecology. 56:215-224
OBJECTIVES: To perform individual record linkage of women undergoing screening with cell-free DNA (cfDNA), combined first-trimester screening (CFTS), second-trimester serum screening (STSS), and/or prenatal and postnatal cytogenetic testing with the
Akademický článek
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Autor:
L, Hui, A, Lindquist, A, Poulton, E, Kluckow, B, Hutchinson, L, Bonacquisto, M D, Pertile, L, Gugasyan, A, Kulkarni, J, Harraway, A, Howden, R, McCoy, F, da Silva Costa, R, Palma-Dias, D, Nisbet, N, Martin, M, Behune, Z, Poulakis, J, Halliday
Publikováno v:
Ultrasound in obstetricsgynecology : the official journal of the International Society of Ultrasound in Obstetrics and Gynecology. 54
Autor:
Ricardo Palma-Dias, J Harraway, Debbie Nisbet, Michael T. Bethune, E Kluckow, Mark D. Pertile, Fiona Norris, L Bonacquisto, Anthea Lindquist, B. Hutchinson, R. McCoy, Cecilia Pynaker, Melody Menezes, Fabricio da Silva Costa, A Poulton, Lisa Hui, L. Gugasyan, A Kulkarni, Jane Halliday, A Howden, Zeffie Poulakis, Nicole Martin
Publikováno v:
American Journal of Obstetrics and Gynecology. 225:527.e1-527.e12
The American College of Obstetricians and Gynecologists and the Society for Maternal-Fetal Medicine recently recommended offering genetic counseling and diagnostic testing for enlarged nuchal translucency at ≥3.0 mm, regardless of previous negative
Autor:
Jane Halliday, Melody Menezes, E Kluckow, Anthea Lindquist, A Howden, Ricardo Palma-Dias, J Harraway, R. McCoy, B. Hutchinson, Debbie Nisbet, Michael T. Bethune, Zeffie Poulakis, Nicole Martin, Fabricio da Silva Costa, Lisa Hui, Mark D. Pertile, L. Gugasyan, A Kulkarni, L Bonacquisto, A Poulton
Publikováno v:
Prenatal diagnosisREFERENCES. 39(13)
OBJECTIVES: To explore the association between timing of diagnosis of common autosomal trisomies, maternal age, and socio-economic status (SES). DESIGN: Retrospective study of cytogenetic diagnoses of trisomy 21 (T21), trisomy 18 (T18), and trisomy 1
Autor:
Lisa Hui, A Howden, Debbie Nisbet, J Harraway, Melody Menezes, B. Hutchinson, Michael T. Bethune, R. McCoy, L. Gugasyan, A Poulton, A Kulkarni, E Kluckow, Jane Halliday, Ricardo Palma-Dias, Anthea Lindquist, Zeffie Poulakis, Mark D. Pertile, L Bonacquisto, Fabricio da Silva Costa, Nicole Martin
Publikováno v:
Human reproduction (Oxford, England). 35(3)
STUDY QUESTION What is the frequency of major chromosome abnormalities in a population-based diagnostic data set of genomic tests performed on miscarriage, fetal and infant samples in a state with >73 000 annual births? SUMMARY ANSWER The overall fre
Autor:
Debbie Nisbet, Jane Halliday, F. da Silva Costa, A Howden, E Kluckow, Marcos Roberto de Menezes, Anthea Lindquist, Zeffie Poulakis, J Harraway, A Poulton, L Bonacquisto, Mark D. Pertile, Michael T. Bethune, Lisa Hui, L. Gugasyan, A Kulkarni, R. McCoy, B. Hutchinson, Ricardo Palma-Dias, Nicole Martin
Publikováno v:
Ultrasound in Obstetrics & Gynecology. 54:14-15
Autor:
J Harraway, Jane Halliday, F. da Silva Costa, M. Behune, A Howden, L Bonacquisto, Nicole Martin, R. McCoy, Debbie Nisbet, E Kluckow, A Poulton, Ricardo Palma-Dias, Anthea Lindquist, B. Hutchinson, Zeffie Poulakis, Mark D. Pertile, L. Gugasyan, A Kulkarni, Lisa Hui
Publikováno v:
Ultrasound in Obstetrics & Gynecology. 54:1-2
OBJECTIVES: Women's choices of prenatal screening and diagnostic pathways have increased in complexity since the introduction of cell-free DNA (cfDNA) screening and chromosomal microarrays. We performed individual record-linkage of women undergoing s
Akademický článek
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Publikováno v:
Ultrasound in Obstetrics & Gynecology. 50:207-207