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References from Identification of the genetic basis of sporadic polydactyly in China by targeted sequencing. Local targets link to admitted publications; unresolved targets remain external evidence.
Polydactyly: phenotypes, genetics and classification
10.1111/cge.12276 · 2014 · External reference
Polydactyly: a genetic study in South America
1973 · External reference
Unresolved reference
External reference
Genetic Overview of Syndactyly and Polydactyly
10.1097/gox.0000000000001549 · 2017 · External reference
Clinical and descriptive genetic study of polydactyly: a Pakistani experience of 313 cases
10.1111/cge.12217 · 2014 · External reference
Mutational screening of GLI3, SHH, preZRS, and ZRS in 102 Chinese children with nonsyndromic polydactyly
10.1002/dvdy.24488 · 2017 · External reference
Clinical genetics of polydactyly: an updated review
10.3389/fgene.2018.00447 · 2018 · External reference
Review of literature: genes related to postaxial polydactyly
10.3389/fped.2015.00008 · 2015 · External reference
Variants in KIAA0825 underlie autosomal recessive postaxial polydactyly
10.1007/s00439-019-02000-0 · 2019 · External reference
10.1002/humu.23924
10.1002/humu.23924 · External reference
10.1136/jmg.2010.079392
10.1136/jmg.2010.079392 · External reference
Clinical exome sequencing identifies novel CREBBP variants in 18 Chinese Rubinstein-Taybi Syndrome kids with high frequency of polydactyly
2019 · External reference
Advances in the molecular genetics of non-syndromic polydactyly
10.1017/erm.2015.18 · 2015 · External reference
Whole exome sequencing identified a novel zinc-finger gene ZNF141 associated with autosomal recessive postaxial polydactyly type A
10.1136/jmedgenet-2012-101219 · 2013 · External reference
Exome sequencing revealed a splice site variant in the IQCE gene underlying post-axial polydactyly type A restricted to lower limb
10.1038/ejhg.2017.83 · 2017 · External reference
Exome sequencing identifies a mutation in OFD1 in a male with Joubert syndrome, orofaciodigital spectrum anomalies and complex polydactyly
10.1038/hgv.2015.69 · 2016 · External reference
Identification of novel mutations in preaxial polydactyly patients through whole-exome sequencing
10.1002/mgg3.690 · 2019 · External reference
10.1093/hmg/ddn411
10.1093/hmg/ddn411 · External reference
10.1038/ng.806
10.1038/ng.806 · External reference
10.1093/nar/gkq603
10.1093/nar/gkq603 · External reference
10.1186/s13073-020-00803-9
10.1186/s13073-020-00803-9 · External reference
10.1093/hmg/ddu733
10.1093/hmg/ddu733 · External reference
10.1038/gim.2015.30
10.1038/gim.2015.30 · External reference
10.1093/bioinformatics/btu684
10.1093/bioinformatics/btu684 · External reference
10.1101/gr.1239303
10.1101/gr.1239303 · External reference
10.1093/nar/gkw937
10.1093/nar/gkw937 · External reference
10.1093/bioinformatics/btp517
10.1093/bioinformatics/btp517 · External reference
An automated method for finding molecular complexes in large protein interaction networks
10.1186/1471-2105-4-2 · 2003 · External reference
10.3389/fcell.2017.00014
10.3389/fcell.2017.00014 · External reference
The molecular basis of human congenital limb malformations
10.1002/wdev.59 · 2012 · External reference
10.1016/j.ydbio.2007.01.019
10.1016/j.ydbio.2007.01.019 · External reference
GLI3-related polydactyly: a review
10.1111/cge.12952 · 2017 · External reference
Molecular analysis expands the spectrum of phenotypes associated with GLI3 mutations
10.1002/humu.21328 · 2010 · External reference
Germline mutations in SUFU cause Gorlin syndrome-associated childhood medulloblastoma and redefine the risk associated with PTCH1 mutations
10.1200/jco.2014.58.2569 · 2014 · External reference
A point mutation in the pre-ZRS disrupts sonic hedgehog expression in the limb bud and results in triphalangeal thumb-polysyndactyly syndrome
10.1038/gim.2018.18 · 2018 · External reference
