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Asphyxiating thoracic dystrophy 5 (sequence analysis of WDR19 gene)
+ info
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Asphyxiating thoracic dystrophy of the newborn type 3 (deletion/duplication in the DYNC2H1 gene)
+ info
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Ataxia telangiectasia (sequencing and CNV analyses of ATM gene)
+ info
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Ataxia telangiectasia like disorder (deletion/duplication analysis on MRE11A gene)
+ info
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Ataxia telangiectasia like disorder (sequence analysis of MRE11A gene)
+ info
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Ataxia with isolated vitamin E deficiency (sequence analysis of TTPA gene)
+ info
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Ataxia with oculomotor apraxia (sequence analysis of APTX gene)
+ info
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Ataxia, posterior column, with retinitis pigmentosa (sequence analysis of FLVCR1 gene)
+ info
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Ataxia-ocular apraxia 2 (AOA2, sequence analysis of SETX gene)
+ info
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Ataxia-oculomotor apraxia type 3 (sequence analysis of PIK3R5 gene)
+ info
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Ataxia-oculomotor apraxia type 4 (sequence analysis of PNKP gene)
+ info
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Ataxia-telangiectasia (deletion/duplication analysis on ATM gene)
+ info
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Athabaskan brainstem dysgenesis syndrome (sequence analysis of HOXA1 gene)
+ info
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Atrial fibrillation (NGS panel of 28 genes)
+ info
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Atrial fibrillation, familial 11 (sequence analysis of GJA5 gene)
+ info
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Atrial fibrillation, familial 6 (sequence analysis of NPPA gene)
+ info
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Atrial fibrillation, familial 7 (sequence analysis of KCNA5 gene)
+ info
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Atrial septal defect 3 (sequence analysis of MYH6 gene)
+ info
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Atrial septal defect 7, with or without AV conduction defects (sequence analysis of NKX2-5 gene)
+ info
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Atrial septal defect 9 (sequence analysis of GATA6 gene)
+ info
