Citation: Molecular and Cellular Pediatrics 2014 1(Suppl 1):A28
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Molecular and Cellular Pediatrics
No abstract.
Citation: Molecular and Cellular Pediatrics 2014 1:4
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Monogenic forms of childhood obesity due to mutations in the leptin gene
Congenital leptin deficiency is a rare autosomal recessive monogenic obesity syndrome caused by mutations in the leptin gene. This review describes the molecular and cellular characteristics of the eight disti...
Citation: Molecular and Cellular Pediatrics 2014 1:3
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Perinatal programming - myths, fact, and future of research
Perinatal programming, i.e., the (epigenetic) modification of (genetic) functions throughout lifetime, suffers from the notion of premature theories and difficult and extensive research strategies.
Citation: Molecular and Cellular Pediatrics 2014 1:2
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The quest for fragile X biomarkers
Fragile X is the most common form of inherited intellectual disability and the leading known genetic cause of autism. There is currently no cure or approved medication for fragile X although various drugs targ...
Citation: Molecular and Cellular Pediatrics 2014 1:1
- ISSN: 2194-7791 (electronic)