Human Genome Epidemiology Literature Finder
Records 1 - 11 (of 11 Records) |
Query Trace: MID1[original query] |
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Duplication of the MID1 first exon in a patient with Opitz G/BBB syndrome. Human genetics 2003 1 112 (3): 249-54. Winter Jennifer, Lehmann Tanja, Suckow Vanessa, Kijas Zofia, Kulozik Andreas, Kalscheuer Vera, Hamel Ben, Devriendt Koen, Opitz John, Lenzner Steffen, Ropers Hans-Hilger, Schweiger Susa |
Genes causing clefting syndromes as candidates for non-syndromic cleft lip with or without cleft palate: a family-based association study. European journal of oral sciences 2008 Dec 116 (6): 507-11. Scapoli Luca, Martinelli Marcella, Arlotti Marzia, Palmieri Annalisa, Masiero Elena, Pezzetti Furio, Carinci Frances |
Hypospadias associated with hypertelorism, the mildest phenotype of Opitz syndrome. Journal of human genetics 2011 May 56 (5): 348-51. Zhang Xufeng, Chen Yougen, Zhao Shentiang, Markljung Ellen, Nordenskjöld Agne |
Human gene copy number spectra analysis in congenital heart malformations. Physiological genomics 2012 Feb . Tomita-Mitchell A, Mahnke DK, Struble CA, Tuffnell ME, Stamm KD, Hidestrand M, Harris SE, Goetsch MA, Simpson PM, Bick DP, Broeckel U, Pelech AN, Tweddell JS, Mitchell ME |
Contribution of polymorphisms in genes associated with craniofacial development to the risk of nonsyndromic cleft lip and/or palate in the Brazilian population. Medicina oral, patología oral y cirugía bucal 2013 May 18 (3): e414-20. Paranaíba Lívia-Máris-Ribeiro, de Aquino Sibele-Nascimento, Bufalino Andreia, Martelli-Júnior Hercílio, Graner Edgard, Brito Luciano-Abreu, e Passos-Bueno Maria-Rita dos Santos, Coletta Ricardo-D, Swerts Mário-Sérgio-Olivei |
Complex genomic rearrangements in the dystrophin gene due to replication-based mechanisms. Molecular genetics & genomic medicine 2014 Nov 2 (6): 539-47. Baskin Berivan, Stavropoulos Dimitri J, Rebeiro Paige A, Orr Jennifer, Li Martin, Steele Leslie, Marshall Christian R, Lemire Edmond G, Boycott Kym M, Gibson William, Ray Peter |
Targeted next?generation sequencing for research and diagnostics in congenital heart disease, and cleft lip and/or palate. Molecular medicine reports 2019 Mar . Bu Haisong, Liu Lin, Hu Shijun, Tan Zhiping, Zhao Tian |
A Genetics-First Approach Revealed Monogenic Disorders in Patients With ARM and VACTERL Anomalies. Frontiers in pediatrics 2020 7 8 310. van de Putte Romy, Dworschak Gabriel C, Brosens Erwin, Reutter Heiko M, Marcelis Carlo L M, Acuna-Hidalgo Rocio, Kurtas Nehir E, Steehouwer Marloes, Dunwoodie Sally L, Schmiedeke Eberhard, Märzheuser Stefanie, Schwarzer Nicole, Brooks Alice S, de Klein Annelies, Sloots Cornelius E J, Tibboel Dick, Brisighelli Giulia, Morandi Anna, Bedeschi Maria F, Bates Michael D, Levitt Marc A, Peña Alberto, de Blaauw Ivo, Roeleveld Nel, Brunner Han G, van Rooij Iris A L M, Hoischen Alexand |
Genetic tests aid in counseling of fetuses with cerebellar vermis defects. Prenatal diagnosis 2020 5 40 (10): 1228-1238. Li Lushan, Fu Fang, Li Ru, Xiao Weiqiang, Yu Qiuxia, Wang Dan, Jing Xiangyi, Zhang Yongning, Yang Xin, Pan Min, Liu Zequn, Liao C |
Foley catheter with noble metal alloy coating for preventing catheter-associated urinary tract infections: a large, multi-center clinical trial. Antimicrobial resistance and infection control 2021 3 10 (1): 40. Kai-Larsen Ylva, Grass Stefan, Mody Bhaumik, Upadhyay Swati, Trivedi Hargovind L, Pal Dilip K, Babu Santosh, Bawari Bikash, Singh Shrawan |
How Far Should We Explore Hypospadias? Next-generation Sequencing Applied to a Large Cohort of Hypospadiac Patients. European urology 2021 1 79 (4): 507-515. Ea Vuthy, Bergougnoux Anne, Philibert Pascal, Servant-Fauconnet Nadège, Faure Alice, Breaud Jean, Gaspari Laura, Sultan Charles, Paris Françoise, Kalfa Nicol |
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- Page last updated:Apr 29, 2024
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