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AMERICAN JOURNAL OF MEDICAL GENETICS PART A
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publication venue for
Recurrent agnathia-Otocephaly caused by DNA replication slippage in PRRX1
. 161A:803-808.
2013
The 3q29 Microdeletion Syndrome: Report of Three New Unrelated Patients and In Silico "RNA Binding'' Analysis of the 3q29 Region
. 155A:1654-1660.
2011
Compound heterozygous mutations in fibulin-4 causing neonatal lethal pulmonary artery occlusion, aortic aneurysm, arachnodactyly, and mild cutis laxa
. 143A:2635-2641.
2007
A 9-year-old male with a duplication of chromosome 3p25.3p26.2: Clinical report and gene expression analysis
. 140A:573-579.
2006
Is it a new syndrome or a clinical variability in cerebro-oculo-nasal syndrome?
. 120A:253-255.
2003
Identity
International Standard Serial Number (ISSN)
1552-4825
Electronic International Standard Serial Number (EISSN)
1552-4833
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journal abbreviation
AM J MED GENET A