All individuals with variants in gene CXCL16

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00204332 58431 PubMed: Rivière 2012 2-generation family, 1 affected, unaffected heterozygous carrier parents M - - - - - - - BRWS see paper;..., no short stature, no microcephaly postnatal; hearing loss, seizures; trigonocephaly, hypertelorism, high-arched eyebrows, congenital ptosis; no coloboma; pachygyria only anterior greater than posterior lissencephaly 1 1 SIB - Livia Famiglietti
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