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1.
Impact of early preeclampsia prediction on medication adherence and behavior change: a survey of pregnant and recently-delivered individuals.
BMC Pregnancy Childbirth
; 24(1): 196, 2024 Mar 13.
Artículo
en Inglés
| MEDLINE | ID: mdl-38481154
2.
Predictive RNA profiles for early and very early spontaneous preterm birth.
Am J Obstet Gynecol
; 227(1): 72.e1-72.e16, 2022 07.
Artículo
en Inglés
| MEDLINE | ID: mdl-35398029
3.
Results of the Genetic Counselor SARS-CoV-2 Impact Survey from the National Society of Genetic Counselors: Progress and penalty during the COVID-19 pandemic.
J Genet Couns
; 30(4): 989-998, 2021 08.
Artículo
en Inglés
| MEDLINE | ID: mdl-34308554
4.
Noninvasive prenatal screening for patients with high body mass index: Evaluating the impact of a customized whole genome sequencing workflow on sensitivity and residual risk.
Prenat Diagn
; 40(3): 333-341, 2020 02.
Artículo
en Inglés
| MEDLINE | ID: mdl-31697845
5.
Technology-Driven Noninvasive Prenatal Screening Results Disclosure and Management.
Telemed J E Health
; 26(1): 8-17, 2020 01.
Artículo
en Inglés
| MEDLINE | ID: mdl-30807262
6.
Correction: Inaccuracies and shortcomings in "Adherence of cell-free DNA noninvasive prenatal screens to ACMG recommendations".
Genet Med
; 21(11): 2663, 2019 11.
Artículo
en Inglés
| MEDLINE | ID: mdl-31217591
7.
Noninvasive prenatal screening at low fetal fraction: comparing whole-genome sequencing and single-nucleotide polymorphism methods.
Prenat Diagn
; 37(5): 482-490, 2017 May.
Artículo
en Inglés
| MEDLINE | ID: mdl-28317136
8.
Inaccuracies and shortcomings in "Adherence of cell-free DNA noninvasive prenatal screens to ACMG recommendations".
Genet Med
; 21(11): 2658-2659, 2019 11.
Artículo
en Inglés
| MEDLINE | ID: mdl-31155613
9.
Response to "Noninvasive prenatal screening at low fetal fraction: comparing whole-genome sequencing and single-nucleotide polymorphism methods".
Prenat Diagn
; 37(7): 727-728, 2017 07.
Artículo
en Inglés
| MEDLINE | ID: mdl-28675624
10.
Strategies to minimize false positives and interpret novel microdeletions based on maternal copy-number variants in 87,000 noninvasive prenatal screens.
BMC Med Genomics
; 11(1): 90, 2018 Oct 19.
Artículo
en Inglés
| MEDLINE | ID: mdl-30340588
11.
Case records of the Massachusetts General Hospital. Weekly clinicopathological exercises. Case 28-2004. Newborn twins with thrombocytopenia, coagulation defects, and hepatosplenomegaly.
N Engl J Med
; 351(11): 1120-30, 2004 Sep 09.
Artículo
en Inglés
| MEDLINE | ID: mdl-15356310
12.
47,XXX associated with malformations.
Am J Med Genet A
; 125A(1): 108-11; author reply 112, 2004 Feb 15.
Artículo
en Inglés
| MEDLINE | ID: mdl-14755479
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