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Lynne A. McInnes et al.
BMC PSYCHIATRY (2007)
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Francesco Timolati et al.
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Consuelo Walss-Bass et al.
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Neuregulin activates erbB2-dependent Src/FAK signaling and cytoskeletal remodeling in isolated adult rat cardiac myocytes
Yukio Kuramochi et al.
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RCP Go et al.
AMERICAN JOURNAL OF MEDICAL GENETICS PART B-NEUROPSYCHIATRIC GENETICS (2005)
Molecular characterization of del(8)(p23.1p23.1) in a case of congenital diaphragmatic hernia
O Shimokawa et al.
AMERICAN JOURNAL OF MEDICAL GENETICS PART A (2005)
Common arterial trunk associated with a homeodomain mutation of NKX2.6
K Heathcote et al.
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Neuregulin 1-erbB signaling and the molecular/cellular basis of schizophrenia
G Corfas et al.
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J Brownlees et al.
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M Tanaka et al.
MOLECULAR AND CELLULAR BIOLOGY (2001)
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JY Wang et al.
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