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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1987 1
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1997 1
1998 1
2001 1
2002 1
2007 2
2008 1
2009 3
2010 2
2011 3
2012 4
2013 6
2014 7
2015 10
2016 4
2017 2
2018 5
2019 8
2020 9
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2023 8
2024 4

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88 results

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Page 1
Paramedian Orofacial Cleft.
Society for Maternal-Fetal Medicine; Benacerraf BR, Bromley B, Jelin AC. Society for Maternal-Fetal Medicine, et al. Am J Obstet Gynecol. 2019 Nov;221(5):B8-B12. doi: 10.1016/j.ajog.2019.08.050. Am J Obstet Gynecol. 2019. PMID: 31679595 No abstract available.
Mutations in Van Der Woude Families From Ethiopia.
Eshete M, Alade A, Abate F, Mossey PA, Awotoye WA, Busch T, Hailu A, Demissie Y, Butali A. Eshete M, et al. J Craniofac Surg. 2022 Mar-Apr 01;33(2):e138-e140. doi: 10.1097/SCS.0000000000008142. J Craniofac Surg. 2022. PMID: 34643600 Free PMC article.
The authors screened all 9 exons of IRF6 and found a novel missense variant in exon 4 (p. Gly65Glu). This variant was predicted to be deleterious/probably damaging by Sift and PolyPhen, respectively. ...
The authors screened all 9 exons of IRF6 and found a novel missense variant in exon 4 (p. Gly65Glu). This variant was predicted to be …
The Likelihood of Orthognathic Surgery After Orofacial Cleft Repair.
Choi KJ, Wlodarczyk JR, Nagengast ES, Wolfswinkel E, Munabi NCO, Yao C, Magee WP 3rd. Choi KJ, et al. J Craniofac Surg. 2021 May 1;32(3):902-906. doi: 10.1097/SCS.0000000000007262. J Craniofac Surg. 2021. PMID: 33235169
A complete understanding of the rate of orthognathic surgery across varying cleft phenotypes is a powerful tool for educating patients and families as to the treatment course that the patient will incur during their lifetime. Understanding the average rates of orthognathic …
A complete understanding of the rate of orthognathic surgery across varying cleft phenotypes is a powerful tool for educating patients and f …
Identification of rare loss-of-function variants in FAM3B associated with non-syndromic orofacial clefts.
Zhao H, He Q, Wu X, Liang X, Jiao Y, Zhang Y, Bao S, Xu L, Hou Y, Zhu X, Ding Y. Zhao H, et al. Genomics. 2023 May;115(3):110630. doi: 10.1016/j.ygeno.2023.110630. Epub 2023 Apr 25. Genomics. 2023. PMID: 37105387 Free article.
In this study, we identify two rare variants in FAM3B (p.Q61R and p.D128G) via target region sequencing of FAM3B on 144 unrelated sporadic patients with non-syndromic OFCs (NSOFCs). Bioinformatic analysis predict that these two variants are likely to be damaging and bioche …
In this study, we identify two rare variants in FAM3B (p.Q61R and p.D128G) via target region sequencing of FAM3B on 144 unrelated sporadic p …
Imaging Factors Affecting Prenatal Counseling in Orofacial Clefts.
Hermann AL, Soupre V, Vande Perre S, Guilbaud L, Quenum-Miraillet G, Blondiaux E, Picard A, Jouannic JM, Dhombres F, Garel C. Hermann AL, et al. Fetal Diagn Ther. 2023;50(2):70-83. doi: 10.1159/000529821. Epub 2023 Feb 28. Fetal Diagn Ther. 2023. PMID: 36854283
INTRODUCTION: We aim to correlate pre- and postnatal data regarding the cleft type and surgical prognostic factors associated to orofacial clefts. METHODS: Retrospective study concerning all cases of orofacial cleft evaluated prenatally (US+/-MRI) between 2015 and 2020 wit …
INTRODUCTION: We aim to correlate pre- and postnatal data regarding the cleft type and surgical prognostic factors associated to orof …
88 results