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Journal Abstract Search
134 related items for PubMed ID: 11223846
1. 46,XX gonadal dysgenesis, short stature, and recurrent metabolic acidosis in two sisters. Hisama FM, Zemel S, Cherniske EM, Vladutiu GD, Pober BR. Am J Med Genet; 2001 Jan 15; 98(2):121-4. PubMed ID: 11223846 [Abstract] [Full Text] [Related]
3. 46,XX gonadal absence: a variant of the XX pure gonadal dysgenesis? Medina M, Kofman-Alfaro S, Pérez-Palacios G. Acta Endocrinol (Copenh); 1982 Apr 15; 99(4):585-7. PubMed ID: 6803492 [Abstract] [Full Text] [Related]
4. Familial ovarian dysgenesis in 46,XX females. Vesely DL, Bower RH, Kohler PO, Char F. Am J Med Sci; 1980 Apr 15; 280(3):157-66. PubMed ID: 6779629 [Abstract] [Full Text] [Related]
9. End-stage renal disease and primary hypogonadism associated with a 46,XX karyotype. Bailey WA, Zwingman TA, Reznik VM, Griswold WR, Mendoza SA, Jones KL, Freidenberg GR. Am J Dis Child; 1992 Oct 15; 146(10):1218-23. PubMed ID: 1329488 [Abstract] [Full Text] [Related]
10. Management of phenotypic female patients with an XY karyotype. Portuondo JA, Neyro JL, Barral A, Gonzalez-Gorospe F, Benito JA. J Reprod Med; 1986 Jul 15; 31(7):611-5. PubMed ID: 3091820 [Abstract] [Full Text] [Related]
15. Premature ovarian failure and ovarian dysgenesis associated with balanced and unbalanced X-6 translocations, respectively: implications for the investigation of ovarian failure. Center JR, McElduff A, Roberts CG. Aust N Z J Obstet Gynaecol; 1994 May 15; 34(2):185-8. PubMed ID: 7980310 [Abstract] [Full Text] [Related]