Clinical Findings and Follow-Up of 46,XY and 45,X/46,XY Testicular Dysgenesis-Reference-Cited by-同舟云学术

Clinical Findings and Follow-Up of 46,XY and 45,X/46,XY Testicular Dysgenesis

Published:2019 Issue:4 Volume:13 Page:171-177
ISSN:1661-5425
Container-title:Sexual Development
language:en
Short-container-title:Sex Dev

Author:

Andrade Juliana G.R.,Fabbri-Scallet Helena,dos Santos Ana P.,Cools Martine,Werner Ralf,Hiort Olaf,de Mello Maricilda P.,Guerra-Júnior Gil,Maciel-Guerra Andrea T.

Publisher

S. Karger AG

Subject

Developmental Biology,Embryology,Endocrinology, Diabetes and Metabolism

Reference36 articles.

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3. Arora R, Datta S, Thukral A, Chakraborty P, Ghosh S, et al: A rare case report of 46XY mixed gonadal dysgenesis. Indian J Endocrinol Metab 17(Suppl1):268-270 (2013).

4. Baetens D, Mladenov W, Delle Chiaie B, Menten B, Desloovere A, et al: Extensive clinical, hormonal and genetic screening in a large consecutive series of 46,XY neonates and infants with atypical sexual development. Orphanet J Rare Dis 9:209 (2014).

5. Bergada C, Cleveland WW, Jones HW, Wilkins L: Gonadal histology in patients with male pseudohermaphroditism and atypical gonadal dysgenesis: relation to theories of sex differentiation. Acta Endocrinol (Copenh) 40:493-520 (1962).

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