The Chromosome 7 Annotation Project
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Chromosome 7 Clinical table -- Search Results

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# Unique IDKaryotypePhenotypeCytogenetic Break FromCytogenetic Break ToMolecular Breakpoint #1Molecular Breakpoint #2Pubmed IDPatient ID          Comments          
1 18496206 46,XY,t(6;7)(p11-p12;q22) autism, severe mental retardation, non-verbal, developmental delay, episodes of extremely violent behaviour, sleep disturbance, submucous cleft palate, wide-set eyes, long philtrum, bifid uvula, coarse facial features with prominent brow and mild synorphoris, long down slanting palpebral fissures, small ears, full lips, broad lateral palatine ridges, pigmented macular lesion on left cheek, occipital midline mass q22   RP11-157M10/G 248P87576C5   18496206 propositus father has same karyotype, affected with learning and behavioural problems, discussion of NPTX2 and TMEM130 as candidate genes Edit