These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
26. [Molecular and cytogenetic study on 5 cases with gonadal dysgenesis: clinical applications of fluorescence in situ hybridization(FISH) and BAC-FISH]. Wu Q; Li J; Wu H; Zhou D; Cai M; Shen Y; Yang C; Ge Y; Kong H; Huang X Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2008 Oct; 25(5):570-2. PubMed ID: 18841574 [TBL] [Abstract][Full Text] [Related]
27. Pure gonadal dysgenesis; clinical and genetic studies. Boczkowski K Mater Med Pol; 1973; 5(3):197-202. PubMed ID: 4749978 [No Abstract] [Full Text] [Related]
28. XYY karyotype in a case of familial hypogonadism. Balodimos MC; Lisco H; Irwin I; Merrill W; Dingman JF J Clin Endocrinol Metab; 1966 Apr; 26(4):443-52. PubMed ID: 5929630 [No Abstract] [Full Text] [Related]
29. [Clinical, biological, histological and genetic studies of De Morsier's syndrome (hypogonadotrophic hypogonadism with anosmia). 7 cases]. de Gennes JL; Turpin G; de Grouchy J; Pialoux P Ann Endocrinol (Paris); 1970; 31(2):234-6. PubMed ID: 5421287 [No Abstract] [Full Text] [Related]
32. A new and simplified method for concealing the hypertrophied clitoris. Ansell JS; Rajfer J J Pediatr Surg; 1981 Oct; 16(5):681-4. PubMed ID: 7310599 [TBL] [Abstract][Full Text] [Related]
33. Pure gonadal dysgenesis (Swyer syndrome) due to microdeletion in the SRY gene: a case report. Mutlu GY; Kırmızıbekmez H; Aydın H; Çetiner H; Moralıoğlu S; Celayir AC J Pediatr Endocrinol Metab; 2015 Jan; 28(1-2):207-10. PubMed ID: 25153220 [TBL] [Abstract][Full Text] [Related]
34. The role of SRY mutations in the etiology of gonadal dysgenesis in patients with 45,X/46,XY disorder of sex development and variants. Nishi MY; Costa EM; Oliveira SB; Mendonca BB; Domenice S Horm Res Paediatr; 2011; 75(1):26-31. PubMed ID: 20699606 [TBL] [Abstract][Full Text] [Related]
35. [Disorders of ossification in gonadal dysgenesis. (Preliminary note)]. Sopeña Ibáñez A; Clavero Núñez JA Acta Ginecol (Madr); 1965 Sep; 16(9):557-68. PubMed ID: 5847890 [No Abstract] [Full Text] [Related]
36. [A case of pure gonadal agenesis of female phenotype and XY karyotype]. Klotz HP; Nathan-Khan J; Jouin D; Bernard S; de Grouchy J Ann Endocrinol (Paris); 1965; 26(5):572-82. PubMed ID: 5853811 [No Abstract] [Full Text] [Related]
37. [Structure and karyotype in male gonadal pathology. (Review and personal contribution)]. Frajese G; Savioli M Folia Endocrinol; 1970 Feb; 23(1):46-59. PubMed ID: 5537052 [No Abstract] [Full Text] [Related]
38. Etiological diagnosis of undervirilized male/XY disorder of sex development. Atta I; Ibrahim M; Parkash A; Lone SW; Khan YN; Raza J J Coll Physicians Surg Pak; 2014 Oct; 24(10):714-8. PubMed ID: 25327912 [TBL] [Abstract][Full Text] [Related]
39. [The male Turner syndrome. Observations on 3 personal cases, including one with a brother with "mixed testicular dysgenesis"]. Matteini M; Maiello M; Salti F Rass Neurol Veg; 1967 Dec; 21(6):402-51. PubMed ID: 5608555 [No Abstract] [Full Text] [Related]