Background Chromosomal microarray analysis (CMA) may detect variants of uncertain
clinical significance (VUS) and susceptibility loci (SL) with incomplete penetrance for�…

Background Chromosomal‐microarray‐analysis (CMA) may reveal susceptibility‐loci (SL) of
varied penetrance for autism‐spectrum‐disorder (ASD) and other neurodevelopmental�…

Background Advanced prenatal genomic technologies can identify risks for adult‐onset (AO)
conditions in the fetus, challenging the traditional purpose of prenatal testing. Professional�…

The nucleus 156Gd was studied with (n, γ) and (n, e−) reactions at the Institut Laue-
Langevin (ILL) in Grenoble. The (d, t) and (d, p) reactions were investigated at the Munich�…

In line with the view that aneuploidy destabilizes the karyotype, initiating an autocatalytic
process that gives rise to further loss and/or gain of chromosomes, we examined whether a�…

Purpose BRCA1/2 founder pathogenic variants (PVs) occur in various populations, but data
on the mutational spectrum in Africans are limited. We examined BRCA1/2 PVs in breast�…

Although1921. lies close to the stability line, only little information on its structure was
hitherto known. This unusual situation is due to the experimental and theoretical difficulties�…

Transcription activity of genes is related to their replication timing, accordingly gene
activation is coupled with a shift from late replication to early replication and vice versa. The�…

Abstract Fragile X syndrome (Fra X) is the most common heritable disease accounting for
mental retardation and is caused by an expanded CGG repeat in the first exon of the�…

A two‐stage process for complete removal of nitrogen from domestic wastewater is
proposed in this paper. The two stages of this process are an aerobic stage using nitrifying�…