Original Research
Published on 06 Jul 2023
Prevalence of geriatric syndromes in frail patients and mortality risks
in Geriatric Medicine
Frontiers in Medicine
doi 10.3389/fmed.2023.1165709
- 3,272 views
- 3 citations
143 articles related to "Diagnostic Center"
Articles
Original Research
Published on 08 May 2023
Safety of COVID-19 vaccine in patients with myasthenia gravis: a self-controlled case series study
in Autoimmune and Autoinflammatory Disorders : Autoimmune Disorders
Frontiers in Immunology
doi 10.3389/fimmu.2023.1141983
- 4,439 views
- 6 citations
Original Research
Published on 30 Nov 2020
Time Intervals Under the Lens at Sweden’s First Diagnostic Center for Primary Care Patients With Nonspecific Symptoms of Cancer. A Comparison With Matched Control Patients
in Cancer Epidemiology and Prevention
Frontiers in Oncology
doi 10.3389/fonc.2020.561379
- 3,458 views
- 3 citations
Original Research
Published on 14 Jan 2022
Clinical Utility of the Prenatal BACs-on-Beads™ Assay in Invasive Prenatal Diagnosis
in Human and Medical Genomics
Frontiers in Genetics
doi 10.3389/fgene.2021.789625
- 3,025 views
- 1 citation
Perspective
Published on 18 May 2022
Clinical Implementation of DPYD Pharmacogenetic Testing to Prevent Early-Onset Fluoropyrimidine-Related Toxicity in Cancer Patients in Switzerland
in Pharmacogenetics and Pharmacogenomics
Frontiers in Pharmacology
doi 10.3389/fphar.2022.885259
- 5,801 views
- 27 citations
Original Research
Published on 20 Dec 2013
Coverage of Cervical Cancer Screening in Catalonia for the Period 2008–2011 among Immigrants and Spanish-Born Women
in Cancer Epidemiology and Prevention
Frontiers in Oncology
doi 10.3389/fonc.2013.00297
- 5,470 views
- 20 citations
Original Research
Published on 07 Sep 2023
Exome sequencing improves genetic diagnosis of congenital orofacial clefts
in Genetics of Common and Rare Diseases
Frontiers in Genetics
doi 10.3389/fgene.2023.1252823
- 5,247 views
- 9 citations
Original Research
Published on 17 Jul 2023
Utilization of multiple genetic methods for prenatal diagnosis of rare thalassemia variants
in Applied Genetic Epidemiology
Frontiers in Genetics
doi 10.3389/fgene.2023.1208102
- 5,803 views
- 6 citations
Original Research
Published on 15 Aug 2025
A retrospective analysis of 38,652 amniotic fluid karyotype
in Human and Medical Genomics
Frontiers in Genetics
doi 10.3389/fgene.2025.1655290
- 2,382 views
- 2 citations
Original Research
Published on 09 May 2023
Genetic diagnosis of fetal microcephaly at a single tertiary center in China
in Genetics of Common and Rare Diseases
Frontiers in Genetics
doi 10.3389/fgene.2023.1112153
- 7,124 views
- 11 citations
Case Report
Published on 29 Apr 2022
Case Report: Two Novel L1CAM Mutations in Two Unrelated Chinese Families With X-Linked Hydrocephalus
in Genetics of Common and Rare Diseases
Frontiers in Genetics
doi 10.3389/fgene.2022.810853
- 3,990 views
- 3 citations
Original Research
Published on 29 Aug 2024
Prenatal diagnosis of the recurrent 1q21.1 microdeletions in fetuses with ultrasound anomalies and review of the literature
in Cytogenomics
Frontiers in Genetics
doi 10.3389/fgene.2024.1448341
- 3,694 views
- 2 citations
Original Research
Published on 12 Aug 2022
Role of preoperative prediction of microvascular invasion in hepatocellular carcinoma based on the texture of FDG PET image: A comparison of quantitative metabolic parameters and MRI
in Medical Physics and Imaging
Frontiers in Physiology
doi 10.3389/fphys.2022.928969
- 5,306 views
- 11 citations
Original Research
Published on 22 Dec 2023
Variant spectrum of F8 and F9 in hemophilia patients from southern China and 26 novel variants
in Human and Medical Genomics
Frontiers in Genetics
doi 10.3389/fgene.2023.1254265
- 4,342 views
- 3 citations
Original Research
Published on 15 Sep 2022
Prenatal diagnosis of 21 fetuses with balanced chromosomal abnormalities (BCAs) using whole-genome sequencing
in Human and Medical Genomics
Frontiers in Genetics
doi 10.3389/fgene.2022.951829
- 3,529 views
- 2 citations
Original Research
Published on 15 Oct 2024
Prenatal diagnosis and postnatal follow-up of 15 fetuses with 16p13.11 microduplication syndrome
in Cytogenomics
Frontiers in Genetics
doi 10.3389/fgene.2024.1486974
- 4,554 views
- 5 citations