• A De Novo Nonsense Mutation in MAGEL2 in a Patient Initially Diagnosed as Opitz-C: Similarities Between Schaaf-Yang and Opitz-C Syndromes
• A single-cell and spatial atlas of autopsy tissues reveals pathology and cellular targets of SARS-CoV-2
• Activity of Selected Nucleoside Analogue ProTides against Zika Virus in Human Neural Stem Cells
• Adams-Oliver Syndrome: Vestigial Tail and Genetics Update
• Alternative Dietary Patterns for Americans: Low-Carbohydrate Diets
• Alternative splicing of BUD13 determines the severity of a developmental disorder with lipodystrophy and progeroid features
• Association of Coronary Stenosis and Plaque Morphology With Fractional Flow Reserve and Outcomes
• Athletic Injuries of the Thoracic Cage
• Bacillus Calmette-Guerin (BCG) vaccination to treat endometriosis
• Beals syndrome with middle and inner ear dysplasia and encephalocele: A case report and review of imaging findings
• Beals-Hecht syndrome
• Beals-Hecht syndrome (congenital contractural arachnodactyly) with additional craniospinal abnormality: a case report
• Beals-Hecht syndrome and choroidal neovascularization
• Beals-Hecht Syndrome: report of a neonatal case
• Bilateral Coronoidectomy by Craniofacial Approach for Hecht Syndrome-Related Trismus
• Breastfeeding with HIV: An Evidence-Based Case for New Policy
• Building Effective Teams in the Real World From Traps to Triumph
• CAUTION ADVISED USING COMBINATION KETOCONAZOLE AND PD-1 INHIBITORS
• Caution in interpretation of disease causality for heterozygous loss-of-function variants in the MYH8 gene associated with autosomal dominant disorder
• Clinical Characteristics and Genetic Analysis of a Family With Birt-Hogg-Dubé Syndrome and Congenital Contractural Arachnodactyly
• Clinical outcomes of Ankoris toric intraocular lens implantation using a computer-assisted marker system
• Comprehensive clinical and molecular assessment of 32 probands with congenital contractural arachnodactyly: report of 14 novel mutations and review of the literature
• Congenital contractural arachnodactyly (Beals-Hecht syndrome) associated with Brown's syndrome
• Congenital contractural arachnodactyly (Beals-Hecht syndrome): a rare connective tissue disorder
• COVID-19 and thyroid function: What do we know so far?
• COVID-19 tissue atlases reveal SARS-CoV-2 pathology and cellular targets
• De Novo Mutations in SLC25A24 Cause a Craniosynostosis Syndrome with Hypertrichosis, Progeroid Appearance, and Mitochondrial Dysfunction
• Detection of Hantavirus during the COVID-19 Pandemic, Arizona, USA, 2020
• Diagnostic strategies and genotype-phenotype correlation in a large Indian cohort of osteogenesis imperfecta
• Discordant loss of mismatch repair proteins in advanced endometrial endometrioid carcinoma compared to paired primary uterine tumors
• DNA Methylation Variation Is Identified in Monozygotic Twins Discordant for Non-syndromic Cleft Lip and Palate
• Effect of Immediate vs Gradual Reduction in Nicotine Content of Cigarettes on Biomarkers of Smoke Exposure: A Randomized Clinical Trial
• Efficacy and safety of the ab interno gelatin stent in severe pseudoexfoliation glaucoma compared to non-pseudoexfoliation glaucoma at 6 months
• Epidemiology of healthcare-associated SARS-CoV-2 outbreaks in Germany between March 2020 and May 2022
• Epigenetic mechanism of FMR1 inactivation in Fragile X syndrome
• Facial analytics based on a coordinate extrapolation system (zFACE) for morphometric phenotyping of developing zebrafish
• Factors Influencing the Outcome of Head and Neck Cancer of Unknown Primary (HNCUP)
• Familial Duodenal Somatostatinomatosis Not Associated With a Known Genetic Syndrome
• Fetal Neuropathology in Zika Virus-Infected Pregnant Female Rhesus Monkeys
• FOXC1 variant in a family with anterior segment dysgenesis and normal-tension glaucoma
• Frailty status as a predictor of 3-month cognitive and functional recovery following spinal surgery: a prospective pilot study
• Genome-Wide Association Study of Non-syndromic Orofacial Clefts in a Multiethnic Sample of Families and Controls Identifies Novel Regions
• Genome-Wide Association Study Reveals Multiple Loci Influencing Normal Human Facial Morphology
• Genome-wide DNA methylation analysis pre- and post-lenalidomide treatment in patients with myelodysplastic syndrome with isolated deletion (5q)
• Genome-wide Enrichment of De Novo Coding Mutations in Orofacial Cleft Trios
• Genome-wide Interaction Study Implicates <em>VGLL2</em> and Alcohol Exposure and <em>PRL</em> and Smoking in Orofacial Cleft Risk
• Germline mosaicism for the c.2021G &gt; A (p.Arg674Gln) mutation in siblings with trismus pseudocamptodactyly
• Humanized three-dimensional scaffold xenotransplantation models for myelodysplastic syndromes
• Identification of a Novel Missense FBN2 Mutation in a Chinese Family with Congenital Contractural Arachnodactyly Using Exome Sequencing
• Immunologic resilience and COVID-19 survival advantage
• Impact of a Mindfulness-Based Weight-Loss Intervention on Sleep Quality Among Adults with Obesity: Data from the SHINE Randomized Controlled Trial
• Impact of low-frequency coding variants on human facial shape
• Impfen bei Immundefizienz : Anwendungshinweise zu den von der Ständigen Impfkommission empfohlenen Impfungen(I) Grundlagenpapier
• Improving the Efficiency of the HIV/AIDS Policy Response: A Guide to Resource Allocation Modeling
• Individuals with nonsyndromic orofacial clefts have increased asymmetry of fingerprint patterns
• It's in the Field of View! Coronary Artery Analysis on Chest Computed Tomographic Angiography
• Lessening Organ Dysfunction With Vitamin C (LOVIT) Trial: Statistical Analysis Plan
• Long-Term Follow-up of Pseudotumor Cerebri Syndrome in Prepubertal Children, Adolescents, and Adults
• MR Angiography Series: Abdominal and Pelvic MR Angiography
• Multiethnic GWAS Reveals Polygenic Architecture of Earlobe Attachment
• Newly diagnosed AIDS with neurosyphilis, Kaposi sarcoma, pancytopenia, oropharyngeal candidiasis, and pseudomonal pneumonia: We shouldn't be seeing this anymore
• Open wide: Anesthetic management of a child with Hecht-Beals syndrome
• Oral microbiome in down syndrome and its implications on oral health
• Peer Support for Post Intensive Care Syndrome Self-Management (PS-PICS): Study protocol for peer mentor training
• PhenX: Host: Biobehavioral measures for tobacco regulatory research
• Polygenic risk impacts PDGFRA mutation penetrance in non-syndromic cleft lip and palate
• Post laser-assisted <em>in-situ</em> keratomileusis dry eye disease and temporary punctal plugs
• Prenatal ultrasound findings in a fetus with congenital contractural arachnodactyly
• Preoperative atropine and non-steroidal anti-inflammatory drugs for the prevention of intraoperative floppy iris syndrome
• Preoperative ocular characteristics predicting the development of intraoperative floppy iris syndrome regardless of alpha-antagonist exposure status
• Psychosocial and behavioral pathways of metabolic syndrome in cancer caregivers
• Rare pancreatic tumors
• Relevance of the time interval between surgery and adjuvant radio (chemo) therapy in HPV-negative and advanced head and neck carcinoma of unknown primary (CUP)
• Responsibility in the Current Epidemic of Language Deprivation (1990-Present)
• Risk Factors for Failure After Surgery in Patients With Diabetic Foot Syndrome
• Rubella Seropositivity in Pregnant Women After Vaccination Campaign in Brazil's Federal District
• Severe congenital contractural arachnodactyly caused by biallelic pathogenic variants in FBN2
• Strategy for the Conservative Treatment of Type-III Camptodactyly in Children with Beals-Hecht Syndrome
• Surgical correction of trismus in a child with Hecht syndrome
• Systematic review and meta-analysis of aortic valve-sparing surgery versus replacement surgery in ascending aortic aneurysms and dissection in patients with Marfan syndrome and other genetic connective tissue disorders
• TCF-1 regulates HIV-specific CD8+ T cell expansion capacity
• The effect of thermo-mechanical device (Tixel) treatment on evaporative dry eye disease - A pilot prospective clinical trial
• The evolutionary neuroscience of domestication
• The expanding phenotype of RNU4ATAC pathogenic variants to Lowry Wood syndrome
• The Female Athlete Triad
• The first reported case of Loeys-Dietz syndrome in a patient with biallelic SMAD3 variants
• The Intersection of the Genetic Architectures of Orofacial Clefts and Normal Facial Variation
• The pathogenicity of SLC38A8 in five families with foveal hypoplasia and congenital nystagmus
• The Positive Rhinovirus/Enterovirus Detection and SARS-CoV-2 Persistence beyond the Acute Infection Phase: An Intra-Household Surveillance Study
• The Use of Inhaled Epoprostenol for Acute Respiratory Distress Syndrome Secondary Due To COVID-19: a Case Series
• Thyroid Hormone Levels During Hospital Admission Inform Disease Severity and Mortality in COVID-19 Patients
• Tooth Agenesis Patterns in Orofacial Clefting Using Tooth Agenesis Code: A Meta-Analysis
• Tracheal intubation in a child with trismus pseudocamptodactyly (Hecht) syndrome
• Trajectory of PaO₂/FiO₂ Ratio in Shock After Angiotensin II
• Trismus-pseudocamptodactyly syndrome: a 20 year follow-up
• Trismus-pseudocamptodctyly syndrome: report of one case
• Verification and diagnostic evaluation of the RealStar^® Middle East respiratory syndrome coronavirus (N gene) reverse transcription-PCR kit 1.0
• Very Severe Differentiation Syndrome in Low Risk Acute Promyelocytic Leukemia - A Peril of Differentiating Therapy
• Whole Exome Sequencing in Individuals with Idiopathic Clubfoot Reveals a Recurrent Filamin B (FLNB) Deletion
• Whole genome sequencing of orofacial cleft trios from the Gabriella Miller Kids First Pediatric Research Consortium identifies a new locus on chromosome 21