Small terminal deletion of 1p and duplication of 1q: cytogenetics, FISH studies, and clinical observations at newborn and at age 16 years
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Maternal pericentric inversion in the origin of an abnormal child due to a recombinant chromosome 1: implications for genetic counseling
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Micropituitarism and cortical dysplasia: an unknown association of two uncommon CNS disorders
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A developmental and genetic classification for malformations of cortical development
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Pachygyria and polymicrogyria in 22q11 deletion syndrome
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A study of 220 patients with polymicrogyria delineates distinct phenotypes and reveals genetic loci on chromosomes 1p, 2p, 6q, 21q and 22q
[Abstract]
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