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Human Genome Epidemiology Literature Finder|Home|PHGKB

Human Genome Epidemiology Literature Finder


Last data update: Dec 2, 2023. (Total: 223599Documents)
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Records 1 - 2 (of 2 Records)

Query Trace: Recurrence and BMP2[original query]
De novo mutations in inhibitors of Wnt, BMP, and Ras/ERK signaling pathways in non-syndromic midline craniosynostosis.
Proceedings of the National Academy of Sciences of the United States of America 2017 8 114 (35): E7341-E7347.
Timberlake Andrew T, Furey Charuta G, Choi Jungmin, Nelson-Williams Carol, , Loring Erin, Galm Amy, Kahle Kristopher T, Steinbacher Derek M, Larysz Dawid, Persing John A, Lifton Richard
Co-occurrence of frameshift mutations in SMAD6 and TCF12 in a child with complex craniosynostosis.
Human genome variation 2018 7 5 14.
Timberlake Andrew T, Wu Robin, Nelson-Williams Carol, Furey Charuta G, Hildebrand Kristi I, Elton Scott W, Wood Jeyhan S, Persing John A, Lifton Richard
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