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A 2.0 Mb microdeletion in proximal chromosome 14q12, involving regulatory elements of FOXG1, with the coding region of FOXG1 being unaffected, results in severe developmental delay, microcephaly, and hypoplasia of the corpus callosum

✍ Scribed by Takagi, Masaki; Sasaki, Goro; Mitsui, Toshikatsu; Honda, Misa; Tanaka, Yoko; Hasegawa, Tomonobu


Book ID
120980770
Publisher
Elsevier Science
Year
2013
Tongue
English
Weight
763 KB
Volume
56
Category
Article
ISSN
1769-7212

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