Human Genome Epidemiology Literature Finder
Records 1 - 11 (of 11 Records) |
Query Trace: HOXD13[original query] |
---|
[Analysis of association between 5' HOXD gene and idiopathic congenital talipes equinovarus]. Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics 2005 Dec 22 (6): 653-6. Wang Li-li, Jin Chun-lian, Liu Li-ying, Zhang Xuan, Ji Shi-jun, Sun Kai-l |
Allelic variants in HOX genes in cryptorchidism. Birth defects research. Part A, Clinical and molecular teratology 2007 Apr 79 (4): 269-75. Wang Yanping, Barthold Julia, Kanetsky Peter A, Casalunovo Tracy, Pearson Erin, Manson Jean |
Study of HOXD genes in autism particularly regarding the ratio of second to fourth digit length. Brain & development 2009 Jun . Sugie Y, Sugie H, Fukuda T, Osawa J |
Hypospadias and genes related to genital tubercle and early urethral development. The Journal of urology 2013 Nov 190 (5): 1884-92. Carmichael Suzan L, Ma Chen, Choudhry Shweta, Lammer Edward J, Witte John S, Shaw Gary |
Mutation screening and array comparative genomic hybridization using a 180K oligonucleotide array in VACTERL association. PloS one 2014 9 (1): e85313. Winberg Johanna, Gustavsson Peter, Papadogiannakis Nikos, Sahlin Ellika, Bradley Frideborg, Nordenskjöld Edvard, Svensson Pär-Johan, Annerén Göran, Iwarsson Erik, Nordgren Ann, Nordenskjöld Agne |
Targeted Resequencing of 29 Candidate Genes and Mouse Expression Studies Implicate ZIC3 and FOXF1 in Human VATER/VACTERL Association. Human mutation 2015 Aug . Hilger Alina C, Halbritter Jan, Pennimpede Tracie, van der Ven Amelie, Sarma Georgia, Braun Daniela A, Porath Jonathan D, Kohl Stefan, Hwang Daw-Yang, Dworschak Gabriel C, Hermann Bernhard G, Pavlova Anna, El-Maarri Osman, Nöthen Markus M, Ludwig Michael, Reutter Heiko, Hildebrandt Friedhe |
[Analysis of HOXD13 gene in polydactyly in dispersion type]. Zhonghua zheng xing wai ke za zhi = Zhonghua zhengxing waike zazhi = Chinese journal of plastic surgery 2015 Jul 31 (4): 255-8. Zhaoliang Liu, Biao Wang, Xiuying Shan, Qicai Liu, Meishui Wang, Houbing Zhe |
A novel microdeletion upstream of HOXD13 in a Chinese family with synpolydactyly. American journal of medical genetics. Part A 2021 9 188 (1): 31-36. Jia Weimin, Zhou Xiaopei, Guo Naiqiang, Zhang Dazhi, Hou Meiqi, Luo Yalin, Peng Xuejie, Yang Xue, Zhang Xianq |
Genome sequencing in families with congenital limb malformations. Human genetics 2021 6 140 (8): 1229-1239. Elsner Jonas, Mensah Martin A, Holtgrewe Manuel, Hertzberg Jakob, Bigoni Stefania, Busche Andreas, Coutelier Marie, de Silva Deepthi C, Elçioglu Nursel, Filges Isabel, Gerkes Erica, Girisha Katta M, Graul-Neumann Luitgard, Jamsheer Aleksander, Krawitz Peter, Kurth Ingo, Markus Susanne, Megarbane Andre, Reis André, Reuter Miriam S, Svoboda Daniel, Teller Christopher, Tuysuz Beyhan, Türkmen Seval, Wilson Meredith, Woitschach Rixa, Vater Inga, Caliebe Almuth, Hülsemann Wiebke, Horn Denise, Mundlos Stefan, Spielmann Mal |
Alpha synuclein (SNCA) rs7684318 variant contributes to Parkinson's disease risk by altering transcription factor binding related with Notch and Wnt signaling. Neuroscience letters 2021 04 750 135802. Naushad Shaik Mohammad, Hussain Tajamul, Alrokayan Salman, Kutala Vijay Kum |
Variants Identified in the HOXC13 and HOXD13 Genes Suggest Association with Cervical Cancer in a Cohort of Mexican Women. Genes 2023 2 14 (2): . Juárez-Rendón Karina Janett, Castro-García Manuel Alejandro, Prada-Ortega Diddier Giovanni, Rivera Gildardo, Ruíz-Godoy Luz María, Enríquez-Cárcamo Virginia Isabel, Reyes-Lopez Miguel Ang |
- Page last reviewed:Feb 1, 2024
- Page last updated:Apr 22, 2024
- Content source: