Below are the most recent publications written about "Urogenital Abnormalities" by people in Profiles.
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Verscaj CP, Velez-Bartolomei F, Bodle E, Chan K, Lyons MJ, Thorson W, Tan WH, Rodig N, Graham JM, Peron A, Quintero-Rivera F, Zackai EH, Thomas MA, Stevens CA, Adam MP, Bird LM, Jones MC, Matalon DR. Characterization of the prenatal renal phenotype associated with 17q12, HNF1B, microdeletions. Prenat Diagn. 2024 02; 44(2):237-246.
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M?nch J, Engesser M, Sch?nauer R, Hamm JA, Hartig C, Hantmann E, Akay G, Pehlivan D, Mitani T, Coban Akdemir Z, T?ys?z B, Shirakawa T, Dateki S, Claus LR, van Eerde AM, Smol T, Devisme L, Franquet H, Atti?-Bitach T, Wagner T, Bergmann C, H?hn AK, Shril S, Pollack A, Wenger T, Scott AA, Paolucci S, Buchan J, Gabriel GC, Posey JE, Lupski JR, Petit F, McCarthy AA, Pazour GJ, Lo CW, Popp B, Halbritter J. Biallelic pathogenic variants in roundabout guidance receptor 1 associate with syndromic congenital anomalies of the kidney and urinary tract. Kidney Int. 2022 05; 101(5):1039-1053.
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Nezhat CH, Hincapie M, Gojayev A, Katz A. Suburethral Endometriosis as Clinical Finding of Extensive Disease. CRSLS. 2022 Jan-Mar; 9(1).
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Connaughton DM, Dai R, Owen DJ, Marquez J, Mann N, Graham-Paquin AL, Nakayama M, Coyaud E, Laurent EMN, St-Germain JR, Blok LS, Vino A, Kl?mbt V, Deutsch K, Wu CW, Kolvenbach CM, Kause F, Ottlewski I, Schneider R, Kitzler TM, Majmundar AJ, Buerger F, Onuchic-Whitford AC, Youying M, Kolb A, Salmanullah D, Chen E, van der Ven AT, Rao J, Ityel H, Seltzsam S, Rieke JM, Chen J, Vivante A, Hwang DY, Kohl S, Dworschak GC, Hermle T, Alders M, Bartolomaeus T, Bauer SB, Baum MA, Brilstra EH, Challman TD, Zyskind J, Costin CE, Dipple KM, Duijkers FA, Ferguson M, Fitzpatrick DR, Fick R, Glass IA, Hulick PJ, Kline AD, Krey I, Kumar S, Lu W, Marco EJ, Wentzensen IM, Mefford HC, Platzer K, Povolotskaya IS, Savatt JM, Shcherbakova NV, Senguttuvan P, Squire AE, Stein DR, Thiffault I, Voinova VY, Somers MJG, Ferguson MA, Traum AZ, Daouk GH, Daga A, Rodig NM, Terhal PA, van Binsbergen E, Eid LA, Tasic V, Rasouly HM, Lim TY, Ahram DF, Gharavi AG, Reutter HM, Rehm HL, MacArthur DG, Lek M, Laricchia KM, Lifton RP, Xu H, Mane SM, Sanna-Cherchi S, Sharrocks AD, Raught B, Fisher SE, Bouchard M, Khokha MK, Shril S, Hildebrandt F. Mutations of the Transcriptional Corepressor ZMYM2 Cause Syndromic Urinary Tract Malformations. Am J Hum Genet. 2020 10 01; 107(4):727-742.
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Cassling C, Shay R, Strassle PD, Voltzke K, Schiff L, Louie M, Carey E. Use of Historic Surgical Times to Predict Duration of Hysterectomy: Stratifying by Uterine Weight. J Minim Invasive Gynecol. 2019 Nov - Dec; 26(7):1327-1333.
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San Agustin JT, Klena N, Granath K, Panigrahy A, Stewart E, Devine W, Strittmatter L, Jonassen JA, Liu X, Lo CW, Pazour GJ. Genetic link between renal birth defects and congenital heart disease. Nat Commun. 2016 Mar 22; 7:11103.
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Dean SJ, Holden KR, Dwivedi A, Dupont BR, Lyons MJ. Acquired microcephaly in blepharophimosis-ptosis-epicanthus inversus syndrome because of an interstitial 3q22.3q23 deletion. Pediatr Neurol. 2014 Jun; 50(6):636-9.
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Clements MB, Chalmers DJ, Meyers ML, Vemulakonda VM. Prenatal diagnosis of cloacal exstrophy: a case report and review of the literature. Urology. 2014 May; 83(5):1162-4.
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Di Renzo D, Aguiar L, Cascini V, Di Nicola M, McCarten KM, Ellsworth PI, Chiesa PL, Caldamone AA. Long-term followup of primary nonrefluxing megaureter. J Urol. 2013 Sep; 190(3):1021-6.
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Dy GW, Rust M, Ellsworth P. Detection and management of pediatric conditions that may affect male fertility. Urol Nurs. 2012 Sep-Oct; 32(5):237-48; quiz 249.