HuGE Literature Finder
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Association of MAMLD1 single-nucleotide polymorphisms with hypospadias in Chinese Han population. Frontiers in bioscience (Landmark edition) 2017 Mar 22 1173-1176. Liu Yidong, Ye Weijing, Wu Ming, Huang Yir |
Polymorphism of 3' UTR of MAMLD1 gene is also associated with increased risk of isolated hypospadias in Indian children: a preliminary report. Pediatric surgery international 2016 Jan . Ratan Simmi K, Sharma Anju, Kapoor Seema, Polipalli Sunil K, Dubey Divya, Mishra Tarun K, Sinha Shandip K, Agarwal Satish |
Is Hypospadias Associated with Prenatal Exposure to Endocrine Disruptors? A French Collaborative Controlled Study of a Cohort of 300 Consecutive Children Without Genetic Defect. European urology 2015 May . Kalfa Nicolas, Paris Françoise, Philibert Pascal, Orsini Mattea, Broussous Sylvie, Fauconnet-Servant Nadège, Audran Françoise, Gaspari Laura, Lehors Hélène, Haddad Myriam, Guys Jean-Michel, Reynaud Rachel, Alessandrini Pierre, Merrot Thierry, Wagner Kathy, Kurzenne Jean-Yves, Bastiani Florence, Bréaud Jean, Valla Jean-Stéphane, Lacombe Gérard Morisson, Dobremez Eric, Zahhaf Amel, Daures Jean-Pierre, Sultan Charl |
[Single-nucleotide polymorphisms of MAMLD1 and hypospadias in Chinese]. Zhonghua nan ke xue = National journal of andrology 2012 Aug 18 (8): 8. Zhuang LK, Fu QH, Wang J, Sun J |
Screening of MAMLD1 mutations in 70 children with 46,XY DSD: identification and functional analysis of two new mutations. PloS one 2012 7 (3): e32505. Kalfa Nicolas, Fukami Maki, Philibert Pascal, Audran Francoise, Pienkowski Catherine, Weill Jacques, Pinto Graziella, Manouvrier Sylvie, Polak Michel, Ogata Totsumo, Sultan Charl |
Polymorphisms of MAMLD1 gene in hypospadias. Journal of pediatric urology 2011 Dec 7 (6): 585-91. Kalfa N, Cassorla F, Audran F, Oulad Abdennabi I, Philibert P, Béroud C, Guys J M, Reynaud R, Alessandrini P, Wagner K, Bréaud J, Valla J S, Morisson Lacombe G, Daures J P, Baskin L, Fukami M, Ogata T, Sultan |
Mutational study of the MAMLD1-gene in hypospadias. European journal of medical genetics 0 53 (3): 122-6. Chen Yougen, Thai Hanh T T, Lundin Johanna, Lagerstedt-Robinson Kristina, Zhao Shengtian, Markljung Ellen, Nordenskjöld Agne |
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