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Cancer risk in individuals with polydactyly: a Swedish population-based cohort study

• Authors : Wachtmeister, A; Tettamanti, G; Nordgren, I

Subjects: Medicin och hälsovetenskap

• Source: British journal of cancer. 131(4):755-762

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Ectrodactyly with Polydactyly in a Dog—Case Description and Description of Surgical Therapy with Resection and Fusion Podoplasty.

• Authors : Wehrenpfennig, Paul¹ (AUTHOR) ; Schmierer, Philipp¹ (AUTHOR)

• Source: Animals (2076-2615). Jun2024, Vol. 14 Issue 11, p1647. 8p.

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A dominant missense variant within LMBR1 related to equine polydactyly.

• Authors : Luan Y; State Key Laboratory of Animal Biotech Breeding, National Engineering Laboratory for Animal Breeding, Laboratory of Animal Genetics, Breeding and Reproduction, Ministry of Agriculture and Rural Affairs, College of Animal Science and Technology, China Agricultural University, Beijing, China.; Zhong L

Subjects: Polydactyly*/Polydactyly*/Polydactyly*/genetics ; Polydactyly*/Polydactyly*/Polydactyly*/veterinary ; Mutation, Missense*

• Source: Communications biology [Commun Biol] 2024 Oct 31; Vol. 7 (1), pp. 1420. Date of Electronic Publication: 2024 Oct 31.Publisher: Nature Publishing Group UK Country of Publication: England NLM ID: 101719179 Publication Model: Electronic Cited Medium: Internet ISSN:

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Acromesomelic Dysplasia With Homozygosity for a Likely Pathogenic BMPR1B Variant: Postaxial Polydactyly as a Novel Clinical Finding.

• Authors : Abdelrazek IM; Department of Human Genetics, Medical Research Institute, Alexandria University, Alexandria, Egypt.; Knaus A

Subjects: Polydactyly*/Polydactyly*/Polydactyly*/genetics ; Polydactyly*/Polydactyly*/Polydactyly*/pathology ; Bone Morphogenetic Protein Receptors, Type I*/Bone Morphogenetic Protein Receptors, Type I*/Bone Morphogenetic Protein Receptors, Type I*/genetics Acromesomelic dysplasia; Polydactyly, Postaxial

• Source: Molecular genetics & genomic medicine [Mol Genet Genomic Med] 2024 Oct; Vol. 12 (10), pp. e70023.Publisher: John Wiley & Sons Country of Publication: United States NLM ID: 101603758 Publication Model: Print Cited Medium: Internet ISSN:

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Retinoblastoma and polydactyly in a child with 46, XY, 15pstk+ karyotype—A case report and literature review.

• Authors : Pi, Xiaohuan¹ (AUTHOR); Zhang, Qiming¹ (AUTHOR); Wang, Xinghua² (AUTHOR)

• Source: Molecular Genetics & Genomic Medicine. Mar2024, Vol. 12 Issue 3, p1-8. 8p.

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A novel missense variant located within the zinc finger domain of the GLI3 gene was identified in a Vietnamese pedigree with index finger polydactyly.

• Authors : Nguyen TN; Department of Life Sciences, University of Science and Technology of Hanoi, Vietnam Academy of Science and Technology, Hanoi, Vietnam.; Tran GS

Subjects: Mutation, Missense* ; Nerve Tissue Proteins*/Nerve Tissue Proteins*/Nerve Tissue Proteins*/genetics ; Pedigree*

• Source: Molecular genetics & genomic medicine [Mol Genet Genomic Med] 2024 Jun; Vol. 12 (6), pp. e2468.Publisher: John Wiley & Sons Country of Publication: United States NLM ID: 101603758 Publication Model: Print Cited Medium: Internet ISSN:

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Epidemiology of congenital polydactyly and syndactyly in Hunan Province, China.

• Authors : Zhou X; Hunan Provincial Maternal and Child Health Care Hospital, Changsha, Hunan Province, 410000, China.; Li T

Subjects: Polydactyly*/Polydactyly*/Polydactyly*/epidemiology ; Syndactyly*/Syndactyly*/Syndactyly*/epidemiology ; Congenital Abnormalities*/Congenital Abnormalities*/Congenital Abnormalities*/epidemiology

• Source: BMC pregnancy and childbirth [BMC Pregnancy Childbirth] 2024 Mar 23; Vol. 24 (1), pp. 216. Date of Electronic Publication: 2024 Mar 23.Publisher: BioMed Central Country of Publication: England NLM ID: 100967799 Publication Model: Electronic Cited Medium: Internet ISSN: 1471-2393

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Tetrapolydactyly: a rare presentation and review of the literature.

• Authors : Seo, Dongkyung^1,2 (AUTHOR) ; Ishii, Riku¹ (AUTHOR); Tada, Keisuke^1,2 (AUTHOR)

• Source: Archives of Hand & Microsurgery. Sep2024, Vol. 29 Issue 3, p187-190. 4p.

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Identification of truncated variants in GLI family zinc finger 3 (GLI3) associated with polydactyly

• Authors : Run-Yan Wang; Qin Xiong; Si-Hua Chang

Subjects: Polydactyly; GLI3; Truncated variant

• Source: Journal of Orthopaedic Surgery and Research, Vol 19, Iss 1, Pp 1-8 (2024)

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Caroli syndrome associated with atrial septal defect and polydactyly: a case report.

• Authors : Ghassa, Ali¹ (AUTHOR) ; Khouri, Lina² (AUTHOR)

• Source: Journal of Medical Case Reports. 5/23/2023, Vol. 17 Issue 1, p1-6. 6p.

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