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Interneuron deficits in patients with the Miller-Dieker syndrome

✍ Scribed by MacLean Pancoast; William Dobyns; Jeffrey A. Golden


Publisher
Springer-Verlag
Year
2005
Tongue
English
Weight
329 KB
Volume
109
Category
Article
ISSN
0001-6322

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We report on a patient prenatally diagnosed with omphalocele, mild cerebral ventriculomegaly, nuchal fold thickening, and cystic changes in the umbilical cord who was found postnatally to have lissencephaly type I. Prenatal chromosome analysis showed a normal male karyotype; however, postnatal high