Human Genome Epidemiology Literature Finder
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Records 1 - 5 (of 5 Records) |
| Query Trace: Abnormalities and PAX2[original query] |
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| PAX2 in 192 Chinese women with Müllerian duct abnormalities: mutation analysis. Reproductive biomedicine online 2012 Aug 25 (2): 219-22. Wang Peng, Zhao Han, Sun Mei, Li Yuan, Chen Zi-Jia |
| Severe prenatal renal anomalies associated with mutations in HNF1B or PAX2 genes. Clinical journal of the American Society of Nephrology : CJASN 2013 Jul 8 (7): 1179-87. Madariaga Leire, Morinière Vincent, Jeanpierre Cécile, Bouvier Raymonde, Loget Philippe, Martinovic Jelena, Dechelotte Pierre, Leporrier Nathalie, Thauvin-Robinet Christel, Jensen Uffe Birk, Gaillard Dominique, Mathieu Michele, Turlin Bruno, Attie-Bitach Tania, Salomon Rémi, Gübler Marie-Claire, Antignac Corinne, Heidet Lauren |
| PAX2 polymorphisms and congenital abnormalities of the kidney and urinary tract in a Brazilian pediatric population: evidence for a role in vesicoureteral reflux. Molecular diagnosis & therapy 2014 Aug 18 (4): 451-7. de Miranda Débora Marques, Dos Santos Júnior Augusto César Soares, Dos Reis Geisilaine Soares, Freitas Izabella Silva, Carvalho Thiago Guimarães Rosa, de Marco Luiz Armando Cunha, Oliveira Eduardo Araújo, Simões E Silva Ana Cristi |
| Clinical Phenotypes Associated to Engrailed 2 Gene Alterations in a Series of Neuropediatric Patients. Frontiers in neuroanatomy 2018 8 12 61. Carratala-Marco Francisco, Andreo-Lillo Patricia, Martinez-Morga Marta, Escamez-Martínez Teresa, Botella-López Arancha, Bueno Carlos, Martinez Salvad |
| Molecular Screening of PAX2 Gene Polymorphism in Primary Vesicoureteral Reflux Patients in Taif Governorate, KSA. Pakistan journal of biological sciences : PJBS 2021 9 24 (4): 492-499. I El-Hallous Ehab, Alharthi Abdulla A, Gaber Ahmed, M Hassan Moham |
- Page last reviewed:Feb 1, 2023
- Page last updated:Sep 25, 2023
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