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本文引用的文献

1
Genome-wide mapping of global-to-local genetic effects on human facial shape.人类面部形状的全基因组范围的整体到局部遗传效应的图谱绘制。
Nat Genet. 2018 Mar;50(3):414-423. doi: 10.1038/s41588-018-0057-4. Epub 2018 Feb 19.
2
Guidelines for morpholino use in zebrafish.斑马鱼中吗啉代使用指南。
PLoS Genet. 2017 Oct 19;13(10):e1007000. doi: 10.1371/journal.pgen.1007000. eCollection 2017 Oct.
3
Zebrafish models of orofacial clefts.口腔颌面部裂隙的斑马鱼模型。
Dev Dyn. 2017 Nov;246(11):897-914. doi: 10.1002/dvdy.24566. Epub 2017 Sep 25.
4
Genetic compensation: A phenomenon in search of mechanisms.基因补偿：一种尚待探寻作用机制的现象。
PLoS Genet. 2017 Jul 13;13(7):e1006780. doi: 10.1371/journal.pgen.1006780. eCollection 2017 Jul.
5
Genome-wide association study of facial morphology reveals novel associations with FREM1 and PARK2.面部形态的全基因组关联研究揭示了与FREM1和PARK2的新关联。
PLoS One. 2017 Apr 25;12(4):e0176566. doi: 10.1371/journal.pone.0176566. eCollection 2017.
6
Heritability maps of human face morphology through large-scale automated three-dimensional phenotyping.通过大规模自动化三维表型分析绘制人类面部形态的遗传力图谱。
Sci Rep. 2017 Apr 19;7:45885. doi: 10.1038/srep45885.
7
Genome-wide analyses of non-syndromic cleft lip with palate identify 14 novel loci and genetic heterogeneity.全基因组分析非综合征性唇腭裂发现 14 个新位点和遗传异质性。
Nat Commun. 2017 Feb 24;8:14364. doi: 10.1038/ncomms14364.
8
High-Throughput Assays to Assess the Functional Impact of Genetic Variants: A Road Towards Genomic-Driven Medicine.评估基因变异功能影响的高通量检测方法：迈向基因组驱动医学之路。
Clin Transl Sci. 2017 Mar;10(2):67-77. doi: 10.1111/cts.12440. Epub 2017 Feb 18.
9
Imputation of orofacial clefting data identifies novel risk loci and sheds light on the genetic background of cleft lip ± cleft palate and cleft palate only.颌面裂数据的插补识别出新的风险位点，并揭示了唇裂±腭裂和单纯腭裂的遗传背景。
Hum Mol Genet. 2017 Feb 15;26(4):829-842. doi: 10.1093/hmg/ddx012.
10
Genome-wide meta-analyses of nonsyndromic orofacial clefts identify novel associations between FOXE1 and all orofacial clefts, and TP63 and cleft lip with or without cleft palate.非综合征性口面部裂隙的全基因组荟萃分析确定了FOXE1与所有口面部裂隙之间以及TP63与伴或不伴腭裂的唇裂之间的新关联。
Hum Genet. 2017 Mar;136(3):275-286. doi: 10.1007/s00439-016-1754-7. Epub 2017 Jan 4.

Craniofacial genetics: Where have we been and where are we going?

作者信息

Weinberg Seth M, Cornell Robert, Leslie Elizabeth J

机构信息

Department of Oral Biology, University of Pittsburgh, Pittsburgh, Pennsylvania, United States of America.

Department of Human Genetics, University of Pittsburgh, Pittsburgh, Pennsylvania, United States of America.

出版信息

PLoS Genet. 2018 Jun 21;14(6):e1007438. doi: 10.1371/journal.pgen.1007438. eCollection 2018 Jun.

DOI:10.1371/journal.pgen.1007438
PMID:29927928
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6013018/
Abstract
摘要