Detalhe da pesquisa
1.
Targeted long-read sequencing identifies missing disease-causing variation.
Am J Hum Genet
; 108(8): 1436-1449, 2021 08 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-34216551
2.
Deletion rescue resulting in segmental homozygosity: A mechanism underlying discordant NIPT results.
Am J Med Genet A
; 182(11): 2666-2670, 2020 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-32798301
3.
Caring for Patients With Serious Mental Illness: Guide for the Oncology Clinician.
Oncology (Williston Park)
; 36(7): 450-459, 2022 07 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-35849778
4.
Changing Face of Invasive Diagnostic Testing in the Era of Cell-Free DNA.
Am J Perinatol
; 34(11): 1142-1147, 2017 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-28718180
5.
The Strategies for Quantitative and Qualitative Remote Data Collection: Lessons From the COVID-19 Pandemic.
JMIR Form Res
; 6(4): e30055, 2022 Apr 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-35394441
6.
Study protocol for a randomized trial of bridge: Person-centered collaborative care for serious mental illness and cancer.
Contemp Clin Trials
; 123: 106975, 2022 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-36307008
7.
Cerebrofacial vascular metameric syndrome is caused by somatic pathogenic variants in PIK3CA.
Cold Spring Harb Mol Case Stud
; 7(6)2021 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-34887309
8.
Computational fluid dynamics modeling aiding surgical planning in a toddler with Parkes Weber syndrome.
J Pediatr Surg Case Rep
; 662021 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-33747785
9.
Maternal Parvovirus B19 Infection Causing First-Trimester Increased Nuchal Translucency and Fetal Hydrops.
Case Rep Obstet Gynecol
; 2019: 3259760, 2019.
Artigo
em Inglês
| MEDLINE | ID: mdl-31360565