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De novo variants predicting haploinsufficiency for DIP2C are associated with expressive speech delay.
Am J Med Genet A. 2024 Feb 29:e63559. doi: 10.1002/ajmg.a.63559. Online ahead of print.
Am J Med Genet A. 2024.
PMID: 38421105
Free article.
Further characterization of Borjeson-Forssman-Lehmann syndrome in females due to de novo variants in PHF6.
Gerber CB, Fliedner A, Bartsch O, Berland S, Dewenter M, Haug M, Hayes I, Marin-Reina P, Mark PR, Martinez-Castellano F, Maystadt I, Karadurmus D, Steindl K, Wiesener A, Zweier M, Sticht H, Zweier C.
Gerber CB, et al.
Clin Genet. 2022 Sep;102(3):182-190. doi: 10.1111/cge.14173. Epub 2022 Jun 14.
Clin Genet. 2022.
PMID: 35662002
Free PMC article.
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Language and thought.
Gerber CB, Snyder DF.
Gerber CB, et al.
Perspect Psychiatr Care. 1970 Sep-Oct;8(5):230-3 passim.
Perspect Psychiatr Care. 1970.
PMID: 5203357
No abstract available.
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