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Journal articles on the topic 'Aphally'

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1

Doums, Claudie, Rabiou Labbo, and Philippe Jarne. "Stability and genetic basis of variability of phally polymorphism in natural populations of the self-fertile freshwater snailBulinus truncatus." Genetical Research 68, no. 1 (1996): 23–33. http://dx.doi.org/10.1017/s0016672300033851.

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SummaryWe investigated the genetic variability for phally polymorphism within and between natural populations of the hermaphrodite self-fertile freshwater snailBulinus truncatus. Phally polymorphism is characterized by the co-occurrence in natural populations of regular hermaphrodite individuals (euphallic) and individuals deprived of the male copulatory organ (aphallic). The two morphs can both self-fertilize and outcross. However, aphallic individuals cannot outcross as males. We examined the variation of the aphally ratio in 22 natural populations from Niger over two successive years. Durin
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2

Doums, Claudie, Philippe Bremond, Bernard Delay, and Philippe Jarne. "The Genetical and Environmental Determination of Phally Polymorphism in the Freshwater Snail Bulinus truncatus." Genetics 142, no. 1 (1996): 217–25. http://dx.doi.org/10.1093/genetics/142.1.217.

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In some species of self-fertile pulmonate snails, two sexual morphs co-occur in natural populations: regular individuals and aphallic individuals that cannot transmit sperm to other snails. Purely aphallic populations therefore reproduce obligatorily by selfing. Understanding the evolution of aphally and selfing in these snails requires a precise knowledge of phally determination. In this paper, we investigate the genetic and environmental determination of aphally in Bulinus truncatus by a survey of the family (offspring) aphally ratio of 233 individuals originating from seven natural populati
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3

Huet, M., N. Le Goïc, and P. E. Gibbs. "Appearance of a genetically-based pollution resistance in a marine gastropod, Nucella lapillus, in south-west Brittany: a new case of Dumpton syndrome." Journal of the Marine Biological Association of the United Kingdom 88, no. 7 (2008): 1475–79. http://dx.doi.org/10.1017/s0025315408002038.

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Most neogastropod species exhibit masculinization of the female when subject to tributyltin (TBT) pollution (a process known as ‘imposex’). To date, the dog-whelk Nucella lapillus is seemingly unique in having a genetic deficiency (termed Dumpton syndrome or DS) that disrupts the development of normal male sex organs, its presence being readily recognizable by the underdevelopment, or non-development (aphally), of the penis, and incomplete formation (non-closure) of the vas deferens, causing a split prostate. In highly contaminated conditions, female carriers of DS can be identified by a lesse
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4

Pokryszko, Beata M. "On the Aphally in the Vertiginidae (Gastropoda: Pulmonata: Orthurethra)." Journal of Conchology 32, no. 6 (1987): 365–75. https://doi.org/10.5962/p.407914.

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5

Gibbs, P. E. "Male genital defect (Dumpton Syndrome) in the dog-whelk Nucella lapillus (Neogastropoda): Mendelian inheritance inferred, based on laboratory breeding experiments." Journal of the Marine Biological Association of the United Kingdom 85, no. 1 (2005): 143–50. http://dx.doi.org/10.1017/s0025315405010969h.

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Laboratory breeding of the dog-whelk, Nucella lapillus, has established that the male-sterilizing Dumpton Syndrome (DS)—underdevelopment, or non-development (aphally), of the penis, incomplete formation (non-closure) of the vas deferens, resulting in a split prostate—can be readily observed in male F1 progeny. Cultivated under high ambient concentrations of the antifouling agent tributyltin (TBT), DS-carrying females can be recognized by their lesser degree of masculinization (imposex): sterilization is thereby avoided. When Dumpton females are crossed, under high ambient TBT, with individuals
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6

Köhler, Frank, and Guilherme Burg Mayer. "Aphally in the stylommatophoran land snail Phaedusa (Clausiliidae: Phaedusinae) in Timor and its systematic implications." Molluscan Research 36, no. 4 (2016): 239–46. http://dx.doi.org/10.1080/13235818.2016.1150771.

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7

Jarne, Philippe, Luc Finot, Christian Bellec, and Bernard Delay. "Aphally Versus Euphally in Self-Fertile Hermaphrodite Snails from the Species Bulinus truncatus (Pulmonata: Planorbidae)." American Naturalist 139, no. 2 (1992): 424–32. http://dx.doi.org/10.1086/285335.

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8

Barreiro, R., M. Quintela, and JM Ruiz. "Aphally and imposex in Nucella lapillus from Galicia (NW Spain):incidence, geographical distribution and consequences for the biomonitoring of TBT contamination." Marine Ecology Progress Series 185 (1999): 229–38. http://dx.doi.org/10.3354/meps185229.

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9

Upreti, Sheetal, Md Fahim Ahmad, Muneer Abas Malik, and Shivani Dogra. "Aphallia with Anal Stenosis and Congenital Cyanotic Heart Disease: A Rare Case Report." Journal of Clinical Neonatology 13, no. 3 (2024): 124–26. http://dx.doi.org/10.4103/jcn.jcn_34_24.

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Aphallia, an extremely rare urogenital anomaly, presents complex challenges in diagnosis and management. This anomaly, often accompanied by other congenital malformations, necessitates multidisciplinary care, and careful consideration of treatment priorities. We describe a case of a neonate diagnosed with aphallia along with anal stenosis, bilateral hydroureteronephrosis, and tetralogy of Fallot. Despite prompt intervention plans, the neonate’s condition deteriorated rapidly, highlighting the urgency and complexity of managing aphallia-associated complications. While embryological insights off
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10

Inkhavilay, Khamla, Thanit Siriboon, Chirasak Sutcharit, Ben Rowson, and Somsak Panha. "The first revision of the carnivorous land snail family Streptaxidae in Laos, with description of three new species (Pulmonata, Stylommatophora, Streptaxidae)." ZooKeys 589 (May 16, 2016): 23–53. https://doi.org/10.3897/zookeys.589.7933.

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The family Streptaxidae in Laos is revised. Twelve species are known, mainly from limestone areas, in the genera Discartemon Pfeiffer, 1856, Perrottetia Kobelt, 1905, Haploptychius Möllendorff, 1906, and Indoartemon Forcart, 1946. Three new species, P. unidentata sp. n. and P. megadentata sp. n. from northern and central Laos, and I. diodonta sp. n. from central Laos, are described. All eight species of these three genera previously recorded from Laos are revised and discussed based on examined material from Laos, Cambodia, Vietnam and Thailand. Type material was examined and lectotypes are de
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11

El Qadiry, R., A. Lalaoui, H. Nassih, A. Bourrahouat, and I. Ait Sab. "A New Presentation: Aphallia, Vesicoureteral Reflux, Rectovesical Fistula, and Adrenal Insufficiency." Case Reports in Pediatrics 2020 (November 23, 2020): 1–3. http://dx.doi.org/10.1155/2020/8826520.

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Aphallia or penile agenesis is a rare congenital malformation with an estimated incidence rate of 1 in 10 to 30 million births. More than half of aphallia cases have associated anomalies including caudal axis, cardiovascular, genitourinary, and gastrointestinal anomalies. The penile agenesis associated with adrenal insufficiency has never been reported in an infant. We report a rare case of a newborn that was diagnosed as a case of aphallia with vesicorectal fistula and vesicoureteral reflux, complicated by adrenal insufficiency with salt-wasting crisis.
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12

Kagantsov, I. M., V. I. Dubrov, V. V. Sizonov, V. G. Bairov, and A. A. Sukhotskaya. "Penile agenesis (afallia) in pueros." Russian Journal of Pediatric Surgery 25, no. 4 (2021): 260–66. http://dx.doi.org/10.18821/1560-9510-2021-25-4-260-266.

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Introduction. Penile agenesis (aphallia) is an extremely rare congenital defect characterized by the complete absence of the penis in a child with a male karyotype 46XY.Material. The analysis of the literature on keywords in the Pubmed and Medline databases was carried out.Results. The incidence of aphallia is estimated 1 out of 10-40 million newborn boys. Aphallia, in spite of its rarity, is a congenital defect which is thoroughly described in the medical literature. The combination of agenesis of the penis with other congenital anomalies often leads to death in such children. Currently, it i
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13

Coquet-Reinier, Benjamin, Thierry Merrot, Kathia Chaumoître, and Pierre Alessandrini. "Atypical aphallia." Pediatric Surgery International 23, no. 11 (2007): 1131–33. http://dx.doi.org/10.1007/s00383-007-1912-z.

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14

Chen, Joanna, Catherine H. Bautista, Ashraf Patel, et al. "Penile Reconstruction in Aphallia: Modification of the De Castro Technique With Large Tissue Expander." Plastic and Reconstructive Surgery - Global Open 13, no. 1 (2025): e6412. https://doi.org/10.1097/gox.0000000000006412.

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Summary: Aphallia is an exceedingly rare congenital malformation. The condition is the result of a sporadic anatomic anomaly during fetal development in a 46, XY male patient with otherwise normal functioning testes and male sexual hormone metabolism. Neophallus reconstruction using the De Castro phalloplasty technique is currently the most accepted treatment modality for this condition. However, most case reports in the literature do not use tissue expansion. To achieve a larger neophallus and possibly decrease the need for secondary phalloplasty postpuberty, tissue expansion should be a stan
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15

Hagelschuer, P., B. Mack-Detlefsen, E. Korsch, A. Ekamp, and T. M. Boemers. "Aphallie – zwei Fallbeispiele." Der Urologe 59, no. 7 (2020): 825–28. http://dx.doi.org/10.1007/s00120-020-01244-3.

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16

Kagantsov, Ilia M., Vitalii I. Dubrov, and Roberto De Castro. "De Castro falloplasty of the with penile agenesis." Russian Journal of Pediatric Surgery, Anesthesia and Intensive Care 10, no. 2 (2021): 183–91. http://dx.doi.org/10.17816/psaic659.

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Introduction. Penile agenesis (aphallia) is an extremely rare congenital disorder. At present, about 100 cases of the anomaly have been described around the world. The incidence of this congenital anomaly is estimated to be one case per 2030 million births. One of the most commonly used reconstructive procedures today is the technique proposed by Roberto De Castro in 2007. In this article, we present a clinical case of aphallia in a boy who underwent phalloplasty.
 Materials and methods. A newborn boy presented with aphallia, combined with abnormal development of both kidneys. At birth, t
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17

Paul Ekka, NishithM, Shital Malua, Pankaj Bodra, and RohitKumar Jha. "Aphallia in an adult." Archives of International Surgery 5, no. 3 (2015): 181. http://dx.doi.org/10.4103/2278-9596.167517.

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18

M, Sasirekha, and Ashok Kumar A. "A CASE REPORT OF APHALLIA." Journal of Evolution of Medical and Dental Sciences 3, no. 12 (2014): 3087–89. http://dx.doi.org/10.14260/jemds/2014/2248.

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19

Skoog, Steven J., and A. Barry Belman. "Aphallia: Its Classification and Management." Journal of Urology 141, no. 3 Part 1 (1989): 589–92. http://dx.doi.org/10.1016/s0022-5347(17)40903-7.

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20

Threatt, Chris B., and John S. Wiener. "Aphallia with congenital urethrorectal fistula." Urology 61, no. 2 (2003): 458–59. http://dx.doi.org/10.1016/s0090-4295(02)02278-1.

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21

Rattan, Kamal N., Pradeep Kajal, Manish Pathak, Yoginder S. Kadian, and Ruchi Gupta. "Aphallia: experience with 3 cases." Journal of Pediatric Surgery 45, no. 1 (2010): e13-e16. http://dx.doi.org/10.1016/j.jpedsurg.2009.10.057.

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22

Holcomb, G. W. "Aphallia: Its classification and management." Journal of Pediatric Surgery 24, no. 11 (1989): 1206–7. http://dx.doi.org/10.1016/s0022-3468(89)80153-8.

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23

Qiang, Shuai, Feng Yong Li, Yu Zhou, Ye Yuan, and Qiang Li. "Congenital absence of the penis (aphallia)." Medicine 98, no. 15 (2019): e15129. http://dx.doi.org/10.1097/md.0000000000015129.

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24

Bizic, M., B. Stojanovic, M. Bencic, V. Kojovic, and M. L. Djordjevic. "Phalloplasty in three cases with aphallia." European Urology Supplements 18, no. 2 (2019): e2356. http://dx.doi.org/10.1016/s1569-9056(19)32055-x.

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25

Gabler, Tarryn, Robyn Charlton, Jerome Loveland, and Ellen Mapunda. "Aphallia: a review to standardize management." Pediatric Surgery International 34, no. 8 (2018): 813–21. http://dx.doi.org/10.1007/s00383-018-4271-z.

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26

Ngom, G., DM Alumeti, AD Kane, and O. Ndour. "Aphallia: A case report and literature review." African Journal of Paediatric Surgery 8, no. 3 (2011): 324. http://dx.doi.org/10.4103/0189-6725.91675.

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27

Sisca, Eni Maria, Eni Maria Sisca, Eni Maria Sisca, et al. "Adult Patients with Aphallia: Were they Fertile?" OnLine Journal of Biological Sciences 22, no. 2 (2022): 214–22. http://dx.doi.org/10.3844/ojbsci.2022.214.222.

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28

Luo, Si-Si, Zhe Yang, Ning Ma, et al. "Congenital aphallia associated with congenital urethrorectal fistula." Medicine 101, no. 7 (2022): e28878. http://dx.doi.org/10.1097/md.0000000000028878.

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29

Bluebond-Langner, Rachel, and Richard Redett. "Phalloplasty in Complete Aphallia and Ambiguous Genitalia." Seminars in Plastic Surgery 25, no. 03 (2011): 196–205. http://dx.doi.org/10.1055/s-0031-1281489.

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30

Rybchenok, V. V., S. L. Kovarsky, K. A. Struyansky, S. P. Blokh, and L. Ya Idris. "De Castro phalloplasty in a child with partial amputation of the penis after electrical burn of the external sex organs." Andrology and Genital Surgery 23, no. 1 (2022): 82–88. http://dx.doi.org/10.17650/1726-9784-2022-23-1-82-88.

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The article describes a method of surgical formation of a neophallus in a child with burned penis and presents a literature review on treatment techniques and patient management tactics for this pathology. De Castro phalloplasty is actively used in children with aphallia and male karyotype 46,ХY, micropenis, and exstrophy–epispadias complex. Uniqueness of the presented clinical demonstration lies in the fact that it is the first time in Russia De Castro phalloplasty was performed in a child with partial amputation of the penis.
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31

Talebpour Amiri, Fereshteh, Davood Nasiry Zarrin Ghabaee, Ramezan Ali Naeimi, Seyed Javad Seyedi, and Seyed Abdollah Mousavi. "Aphallia: Report of three cases and literature review." International Journal of Reproductive BioMedicine 14, no. 4 (2016): 279–84. http://dx.doi.org/10.29252/ijrm.14.4.279.

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32

Gérard-Blanluet, Marion, Véronique Lambert, Suonavy Khung-Savatovsky, et al. "Aphallia, Lung Agenesis and Multiple Defects of Blastogenesis." Fetal and Pediatric Pathology 30, no. 1 (2011): 22–26. http://dx.doi.org/10.3109/15513815.2010.494698.

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33

Faiz, Nameer, and Amarendra Kumar. "Aphallia: Case report and review of the literature." Saudi Surgical Journal 3, no. 1 (2015): 13. http://dx.doi.org/10.4103/2320-3846.153801.

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34

Oliveira, Diego Estevam Gomes, Marcela Leal da Cruz, Riberto Liguori, et al. "Neophalloplasty in boys with aphallia: A systematic review." Journal of Pediatric Urology 12, no. 1 (2016): 19–24. http://dx.doi.org/10.1016/j.jpurol.2015.10.003.

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35

Descamps, M. J. L., P. M. Hayes, and Don A. Hudson. "Phalloplasty in complete aphallia: pedicled anterolateral thigh flap." Journal of Plastic, Reconstructive & Aesthetic Surgery 62, no. 3 (2009): e51-e54. http://dx.doi.org/10.1016/j.bjps.2007.04.014.

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36

Biswal, Sasmita. "Congenital Aphalia associated with Thoracic Hemivertebrae -A Case Report." International Journal of Contemporary Surgery 1, no. 1 (2013): 46. http://dx.doi.org/10.5958/j.2321-1024.1.1.006.

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37

Patil, Prashant Sadashiv, Abhaya Gupta, Gursev Sandlas, et al. "Aphallia (Penile agenesis): A preliminary report of three cases." Pediatric Urology Case Reports 4, no. 1 (2017): 243. http://dx.doi.org/10.14534/pucr.2017124185.

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38

Nappo, Simona, Roberto De Castro, and Paolo Caione. "Early one-stage total phalloplasty in infants with aphallia." Journal of Pediatric Urology 3 (April 2007): S84—S85. http://dx.doi.org/10.1016/j.jpurol.2007.01.157.

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39

Joshi, Aditya, Jody Gross, and James Vincent Thomalla. "Congenital Aphallia: Review of Pathogenesis and Current Treatment Guidelines." Urology 86, no. 2 (2015): 384–87. http://dx.doi.org/10.1016/j.urology.2015.04.031.

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40

Wang, Hongliang, Kaimin Guo, Jiping Wang, Lingyun Liu, and Fubiao Li. "Aphallia in an adult male with 46,XY karyotype." International Journal of Urology 18, no. 7 (2011): 540–42. http://dx.doi.org/10.1111/j.1442-2042.2011.02785.x.

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41

Carter, Lauren, and Caitlin Bozick. "P140: Aphallia: A complex case of a rare anomaly." Genetics in Medicine Open 1, no. 1 (2023): 100169. http://dx.doi.org/10.1016/j.gimo.2023.100169.

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42

Ajaj, Omar. "A case of Aphallia associated with neonatal intestinal obstruction." Journal of Neonatal Surgery 12 (January 6, 2023): 6. http://dx.doi.org/10.47338/jns.v12.1119.

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43

Pan, Pradyumna. "Aphallia: An Extremely Rare Congenital Anomaly. Report of Two Cases." Acta Scientific Paediatrics 2, no. 9 (2019): 67–69. http://dx.doi.org/10.31080/aspe.2019.02.0133.

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44

Shilpa, Kalane, Joshi Rajan, and Rajhans Arati. "A rare case report of aphallia with Horse-shoe kidney." Journal of Clinical Neonatology 5, no. 1 (2016): 55. http://dx.doi.org/10.4103/2249-4847.173277.

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45

Doums, Claudie, Mireille-Ange Perdieu, and Philippe Jarne. "RESOURCE ALLOCATION AND STRESSFUL CONDITIONS IN THE APHALLIC SNAILBULINUS TRUNCATUS." Ecology 79, no. 2 (1998): 720–33. http://dx.doi.org/10.1890/0012-9658(1998)079[0720:raasci]2.0.co;2.

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46

Bhandari, Mahendra, Rahul Janak Sinha, and Vishwajeet Singh. "Urethral Reconstruction in Patients Suffering from Aphallia: A Reconstructive Challenge." Urologia Internationalis 87, no. 4 (2011): 475–80. http://dx.doi.org/10.1159/000330941.

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47

Reiner, W. G. "Commentary to ‘Neophalloplasty in boys with aphallia: A systematic review’." Journal of Pediatric Urology 12, no. 1 (2016): 25. http://dx.doi.org/10.1016/j.jpurol.2015.10.001.

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48

Friedman, Ariella A., Paul F. Zelkovic, Edward F. Reda, Israel Franco, and Lane S. Palmer. "Male and female aphallia associated with severe urinary tract dysplasia." Journal of Pediatric Urology 12, no. 4 (2016): 268.e1–268.e7. http://dx.doi.org/10.1016/j.jpurol.2016.04.040.

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49

Singh, Vishwajeet, Deepak Sharanappa Nagathan, Rahul Janak Sinha, and Dheeraj Kumar Gupta. "Tricholithobezoar: An Unusual Late Complication of Neourethral Reconstruction in Aphallia." Korean Journal of Urology 54, no. 5 (2013): 345. http://dx.doi.org/10.4111/kju.2013.54.5.345.

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50

Laranjeiro, Filipe, Paula Sánchez-Marín, Ana Barros, et al. "Triphenyltin induces imposex in Nucella lapillus through an aphallic route." Aquatic Toxicology 175 (June 2016): 127–31. http://dx.doi.org/10.1016/j.aquatox.2016.03.005.

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