Background Fetal structural anomalies, which are detected by ultrasonography, have a
range of genetic causes, including chromosomal aneuploidy, copy number variations (CNVs; …

This volume is the fourth in a series related to a project to create a Regional University Network
on Governance and Management of Higher Education in South East Europe. It is both an …

… Carolyn Campbell … On behalf of the steering group it is my pleasure to extend our
thanks to Carolyn Campbell and Marijk van der Wende who undertook to make this report. …

The purpose of this study was to quantify the sagittal angular displacement of the head (cranio-cervical
flexion) for the five incremental stages of the cranio-cervical flexion test (CCFT). …

Purpose Increasing numbers of genes are being implicated in Mendelian disorders and
incorporated into clinical test panels. However, lack of evidence supporting the gene-disease …

Background The 15q11.2 deletion is frequently identified in the neurodevelopmental clinic.
Case–control studies have associated the 15q11.2 deletion with neurodevelopmental …

Recognizing the complexities of critical social work the authors use a metaphor of a traffic
circle to survey the fundamental values, assumptions, theories, concepts, principles, and …

Background: The common intronic deletion, MYBPC3 Δ25 , detected in 4% to 8% of South
Asian populations, is reported to be associated with cardiomyopathy, with ≈7-fold increased …

Study Objective: To determine the efficacy of a short course of prednisone followed by
recombinant interferon treatment in patients with chronic type B hepatitis. Design: Randomized, …

Background Noninvasive ventilation (NIV) is the first-line treatment of adult patients with
exacerbations of cystic fibrosis (CF). High-flow nasal oxygen therapy (HFNT) might benefit …