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Date: 2005
Language: eng
Resource Type: journal article
Identifier: uon:574
Description: Opitz syndrome (OS; MIM 1454 10 and MIM 300000) is a congenital midline malformation syndrome characterized by hypertelorism, hypospadias, cleft lip/palate, laryngotracheoesophageal (LTE) abnormalitie... More
Reviewed: Reviewed
Date: 2005
Language: eng
Resource Type: journal article
Identifier: uon:276
Description: In families with nonsyndromic X-linked mental retardation (NS-XLMR), >30% of mutations seem to cluster on proximal Xp and in the pericentric region. In a systematic screen of brain-expressed genes fro... More
Reviewed: Reviewed
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