P018-SHOX
Idiopathic growth retardation
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P183-EDA
Ectodermal dysplasia, x-linked (XLHED)
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P184-JAG1
Alagille Syndrome (AGS)
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P147-1p36
1p36 deletion syndrome
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P128-CYP450
Cytochrome P-450
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P244-AIP-MEN1
Multiple endocrine neoplasia (MEN)
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P163-GJB-WFS1
Hearing loss
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P016-VHL
Von Hippel-Lindau Syndrome
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P070-Telomere-5
Broad subtelomeric screening
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P051-Parkinson mix 1
Parkinson disease, familial
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P054-FOXL2-TWIST1
Ophthalmogenetic anomalies
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