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kw.\*:("46, XY DSD")

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5 α-Reductase Type 2 Deficiency: Response to Dihydrotestosterone GelVUPPUTURI, Madhavarao; KANDEPU, Madhurima; HARIKISHORE REDDY DEVIREDDY et al.Indian journal of pediatrics. 2014, Vol 81, Num 8, pp 821-823, issn 0019-5456, 3 p.Article

Mutations in the TSPYL1 gene associated with 46,XY disorder of sex development and male infertilityVINCI, Giovanna; BRAUNER, Raja; TAR, Attila et al.Fertility and sterility. 2009, Vol 92, Num 4, pp 1347-1350, issn 0015-0282, 4 p.Article

Molecular Analysis of the SRD5 A2 in 46,XY Subjects With Incomplete Virilization: The P212R Substitution of the Steroid 5α-Reductase 2 May Constitute an Ancestral Founder Mutation in Mexican PatientsVILCHIS, Felipe; RAMOS, Luis; MENDEZ, Juan Pablo et al.Journal of andrology. 2010, Vol 31, Num 4, pp 358-364, issn 0196-3635, 7 p.Article

Two siblings with 46,XY DSD, congenital adrenal hypoplasia, aniridia, craniofacial, and skeletal abnormalities and intrauterine growth retardation : A new syndrome?COMAN, David J; WHITE, Susan M; AMOR, David J et al.American journal of medical genetics. Part A. 2007, Vol 143, Num 18, pp 2085-2088, issn 1552-4825, 4 p.Article

46, XY gonadal dysgenesis: new SRY point mutation in two siblings with paternal germ line mosaicismSTOPPA-VAUCHER, S; AYABE, T; PAQUETTE, J et al.Clinical genetics. 2012, Vol 82, Num 6, pp 505-513, issn 0009-9163, 9 p.Article

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