A war of words : Dutch pro-Boer propaganda and the South African war (1899-1902) - Cover

In this review we highlight twelve genetic syndromes in which sufficient phenomenological data are available: Angelman Syndrome (AS), Cornelia de Lange Syndrome (CdLS),

The first clinical reports on SMC1A described that variants in this gene cause X-linked Cornelia de Lange syndrome or a mild variant of Cornelia de.. Lange

For Dutch participants with SMC1A variants we performed direct in-person assessments of cognition, autism, and added an interview and questionnaire on adaptive behaviour and

Alignment of the corresponding mutated NFIX proteins in Malan syndrome and Marshall-Smith syndrome predicts that despite the overlap in the genomic positions of variants, the

individuals with the classic Cornelia de Lange syndrome (CdLS) phenotype, the first- line molecular diagnostic approach should be next- generation sequencing (NGS)-based

Alex Levin Paediatric Ophthalmology and Ocular Genetics, Wills Eye Hospital, Thomas Jefferson University, Philadelphia, PA, USA Mary Levis Wicomico County Board of

The table explains: general study information (author, year, aim and study method), characteristics of study population (entity, acquisition, selection criteria, confirmation od

Experiments on the MSR-VTT validation set and the blind test on the test set support conclusions as follows. The proposed early embedding and late reranking solution can