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- Journal Article5,609
- Volume 161:Issue 1(2013:Jan.)45
- Volume 161:Issue 10(2013:Oct.)49
- Volume 161:Issue 11(2013:Nov.)35
- Volume 161:Issue 12(2013:Dec.)90
- Volume 161:Issue 2(2013:Feb.)32
- Volume 161:Issue 3(2013:Mar.)39
- Volume 161:Issue 4(2013:Apr.)54
- Volume 161:Issue 5(2013:May)53
- Volume 161:Issue 6(2013:Jun.)54
- Volume 161:Issue 7(2013:Jul.)54
- 616.14205 5,609
- Medical genetics -- Periodicals 5,609
- 14q11.2q13.1 triplication -- 14q11.2q13.1 tetrasomy -- SNP array -- UPD -- imprinted gene -- paternal origin 2
- 18q12.2 deletion -- array CGH -- autism -- CELF4 -- RNA‐binding proteins 2
- 1q21.3 -- developmental delay -- GATAD2B -- hypotonia -- microdeletion -- non‐homologous end joining -- SNP array -- TPM3 2
- AEC -- Bartsocas‐Papas syndrome -- CHAND syndrome -- ectodermal dysplasia -- RIPK4 2
- Al‐Raqad syndrome -- DCPS -- 11q24.2 -- genomic microarray -- CMA 2
- Angelman syndrome -- mosaic Angelman -- atypical Angelman -- imprinting center defect -- hyperphagia 2
- BBS9 -- BMP signaling -- BMP2 -- craniofacial development -- craniosynostosis -- enhancer 2
- CHARGE syndrome -- gastrointestinal -- reflux -- tube feeding 2