Abstract The relativistic Hartree-Bogoliubov (RHB) model is extended to include density-
dependent meson-nucleon couplings. The effective Lagrangian is characterized by a …

Advances in genomic analyses based on next‐generation sequencing and integrated omics
approaches, have accelerated in an unprecedented way the discovery of causative genes of …

Smith-Magenis syndrome (SMS) is a complex genetic disorder characterized by distinctive
physical features, developmental delay, cognitive impairment, and a typical behavioral …

We describe a 6-year-old boy carrying a de novo 5Mb interstitial deletion of chromosome
8p23. 1 identified by means of oligonucleotide array comparative genomic hybridisation …

Allergic bronchopulmonary aspergillosis (ABPA) is caused by a dominant Th2 immune
response to antigens derived from the opportunistic mold Aspergillus, most commonly …

Of 2,800 patients admitted to hospital with a diagnosis of seizure, 1.1%(30/2,800) sustained
fracture. Of these, 0.5%(15/2,800) had fracture due to direct trauma, 0.3%(7/2,800) had …

Sex chromosome abnormalities have been advocated to be involved in the striking female
prevalence of primary biliary cirrhosis (PBC) and women with PBC manifest an increased X …

Background: Chromosome 13q deletion is associated with varying phenotypes, which seem
to depend on the location of the deleted segment. Although various attempts have been …

Rubinstein‐Taybi syndrome (RSTS) is a rare congenital neurodevelopmental disorder
characterized by postnatal growth deficiency, skeletal abnormalities, dysmorphic features …

The human genome contains a large number of sequences related to the cDNA for High
Mobility Group 1 protein (HMG1), which so far has hampered the cloning and mapping of the …