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Genetic heterogeneity has made the identification of genes related to hearing impairment a challenge. In the absence of a clear phenotypic aetiology, recurrence risk estimates are often based on family segregation and may be imprecise. We profiled by oligonucleotide array‐CGH patients presenting non‐syndromic hearing loss with presumptive autosomal recessive (n = 50) or autosomal dominant (n = 50)...
The psychological research literature on children born with disorders of sex development (DSDs) has largely focused on their psychosexual development, with less attention given to other aspects of their psychosocial well-being, including the presence of clinical range behaviour problems. Children with DSDs may be at risk for behaviour problems for several reasons: (1) the chronic nature of their medical...
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