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Familial Miller-Dieker syndrome associated with pericentric inversion of chromosome 17.
Oculocerebrocutaneous syndrome: the brain malformation defines a core phenotype.
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Familial Miller-Dieker syndrome associated with pericentric inversion of chromosome 17.
Familial Miller-Dieker syndrome associated with pericentric inversion of chromosome 17. Am J Med Genet. 1986 Apr; 23(4):853-9.
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PubMed
subject areas
Abnormalities, Multiple
Brain
Chromosome Aberrations
Chromosome Banding
Chromosomes, Human, 16-18
Face
Humans
Infant, Newborn
Male
Syndrome
authors with profiles
William B. Dobyns