All individuals with variants in gene MIR542

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00050635 - PubMed: DDDS 2015, Journal: DDDS 2015 family, 1 affected F - United Kingdom (Great Britain) - - - Decipher - ? global developmental delay, joint hypermobility, sparse scalp hair, sparse lateral eyebrow, highly arched eyebrow, strabismus, edema, spontaneous neonatal pneumothorax, umbilical hernia, hypopigmentation of the skin, 3-4 toe syndactyly, sandal gap, ventriculomegaly, generalized neonatal hypotonia, nocturnal hypoventilation, hip dysplasia, unilateral ptosis, upslanted palpebral fissure, inverted nipples 1 1 Johan den Dunnen
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