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Year | Number of Results |
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2018 | 2 |
2019 | 1 |
2025 | 0 |
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Haploinsufficiency of NCOR1 associated with autism spectrum disorder, scoliosis, and abnormal palatogenesis.
Am J Med Genet A. 2018 Nov;176(11):2466-2469. doi: 10.1002/ajmg.a.40354. Epub 2018 Oct 5.
Am J Med Genet A. 2018.
PMID: 30289594
SATB2-associated syndrome in patients from Japan: Linguistic profiles.
Yamada M, Uehara T, Suzuki H, Takenouchi T, Yoshihashi H, Suzumura H, Mizuno S, Kosaki K.
Yamada M, et al.
Am J Med Genet A. 2019 Jun;179(6):896-899. doi: 10.1002/ajmg.a.61114. Epub 2019 Mar 7.
Am J Med Genet A. 2019.
PMID: 30848049
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Ablepharon and craniosynostosis in a patient with a localized TWIST1 basic domain substitution.
Takenouchi T, Sakamoto Y, Sato H, Suzuki H, Uehara T, Ohsone Y, Kosaki K.
Takenouchi T, et al.
Am J Med Genet A. 2018 Dec;176(12):2777-2780. doi: 10.1002/ajmg.a.40525. Epub 2018 Nov 18.
Am J Med Genet A. 2018.
PMID: 30450715
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