PubMed · 2013 · 10 citations · 15 references
Life SciencesGeneticsMolecular GeneticsHuman GeneticsMedical GeneticsPediatric GeneticsCongenital Craniofacial AnomaliesCraniofacial Developmental GeneticsGenetic DisordersLip DevelopmentPalate GeneticsSingle-gene Craniofacial DisordersCleft Lip SyndromesCleft Palate SyndromesCongenital Craniofacial Anomalies GeneticsCraniofacial Developmental AnomaliesGene Deletion SyndromesMicroarray AnalysisMicrodeletion SyndromesSyndromic Craniofacial Disorders
, are described in relationship to the very few cases of 20q13 deletion reported in the literature. Deletion of this region may play an important role in neurodevelopment and function and in causing specific craniofacial features.
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Common genetic variants on 5p14.1 associate with autism spectrum disorders
Kai Wang, Haitao Zhang, Deqiong Ma et al. · Nature · 2009 · 973 citations · Full text
The imprinted signaling protein XLαs is required for postnatal adaptation to feeding
Antonius Plagge, Emma Gordon, Wendy Dean et al. · Nature Genetics · 2004 · 268 citations
Jo Peters, Stephanie F. Wroe, Christine A. Wells et al. · Proceedings of the National Academy of Sciences · 1999 · 241 citations · Full text