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A study of ring 20 chromosome karyotype with epilepsy

✍ Scribed by HIROSHI YAMADERA; KEIKO KOBAYASHI; KENJI SUGAI; HAJIME SUDA; SUNAO KANEKO

Book ID
108961576
Publisher
John Wiley and Sons
Year
1998
Tongue
English
Weight
386 KB
Volume
52
Category
Article
ISSN
1323-1316

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## To the Editor: The Opitz or BBBG syndrome is an autosomal dominant disorder characterized by facial anomalies and multiple congenital abnormalities. Recent evidence would suggest that the Opitz and BBB syndromes form a spectrum of the same condition Verloes et al., 19891 and it has been sugges