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Nucleic acids research, ISSN 0305-1048, 12/2018, Volume 46, Issue 22, pp. 11659 - 11670
N-6-methyldeoxyadenosine (6mA) is a wel-lcharacterized DNA modification in prokaryotes but reports on its presence and function in mammals have been... 
PROTEIN | DNA METHYLATION | N-6-METHYLADENINE | N-6-ADENINE | ALKBH1 | BIOCHEMISTRY & MOLECULAR BIOLOGY | GENE-EXPRESSION | RETROTRANSPOSONS | ADENINE
Journal Article
Pediatric Neurology, ISSN 0887-8994, 05/2019, Volume 94, pp. 64 - 69
Arrest of fetal brain development and the fetal brain disruption sequence describe a severe phenotype involving microcephaly, occipital bone prominence, and... 
Fetal brain disruption sequence | Congenital microcephaly | Congenital disorder of glycosylation | Fetal magnetic resonance imaging | DIAGNOSIS | PEDIATRICS | CONGENITAL DISORDER | SERUM | ZIKA VIRUS-INFECTION | CLINICAL NEUROLOGY | Brain | Brain research | Genetic disorders | Genomics | Physiological aspects | Lipids | Genetic screening
Journal Article
Nature Reviews Genetics, ISSN 1471-0056, 11/2011, Volume 12, Issue 11, pp. 745 - 755
Journal Article
Pediatric neurology, 12/2018
Arrest of fetal brain development and the fetal brain disruption sequence describe a severe phenotype involving microcephaly, occipital bone prominence, and... 
Journal Article
Human Molecular Genetics, ISSN 0964-6906, 10/2010, Volume 19, Issue 2, pp. R119 - R124
Massively parallel sequencing has enabled the rapid, systematic identification of variants on a large scale. This has, in turn, accelerated the pace of gene... 
GENE | DATABASE | GENOMES | DNA | BIOCHEMISTRY & MOLECULAR BIOLOGY | GENETICS & HEREDITY | ENRICHMENT | MUTATIONS | INHERITANCE | CONSTRAINT | TRAITS | CAPTURE | Rare Diseases - genetics | High-Throughput Nucleotide Sequencing | Humans | Genome, Human - genetics
Journal Article