Re-evaluation of MRX36 family after discovery of an ARX gene mutation reveals mild neurological features of Partington syndrome
- PMID: 12376949
- DOI: 10.1002/ajmg.10628
Re-evaluation of MRX36 family after discovery of an ARX gene mutation reveals mild neurological features of Partington syndrome
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Linkage analysis in three families with nonspecific X-linked mental retardation.Am J Med Genet. 1996 Jul 12;64(1):137-46. doi: 10.1002/(SICI)1096-8628(19960712)64:1<137::AID-AJMG24>3.0.CO;2-N. Am J Med Genet. 1996. PMID: 8826464
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