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Journal Abstract Search

129 related items for PubMed ID: 6803492

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  • 3. 46,XX gonadal dysgenesis with epibulbar dermoid.
    Quayle SA, Copeland KC.
    Am J Med Genet; 1991 Jul 01; 40(1):75-6. PubMed ID: 1909490
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  • 4. 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
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  • 6. Further evidence for differential regulation of follicle-stimulating hormone (FSH) and luteinizing hormone (LH): increased FSH and decreased LH levels in a patient with familial pure gonadal dysgenesis.
    Popovic V, Micic D, Damjanovic S, Calovic L, Rolovic Z, Mijovic A, Petakov M, Manojlovic D, Micic J.
    Postgrad Med J; 1992 Nov 15; 68(805):925-7. PubMed ID: 1494516
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  • 7. Familial 46,XX gonadal dysgenesis.
    Portuondo JA, Neyro JL, Benito JA, de los Rios A, Barral A.
    Int J Fertil; 1987 Nov 15; 32(1):56-8. PubMed ID: 2880817
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  • 8. [Comparison of hormonal levels of LH and FSH with cytogenetic findings in patients with gonadal dysgenesis].
    Santavý J, Fingerová H, Knopová V, Fargasová I, Zenísek L.
    Bratisl Lek Listy; 1985 May 15; 83(5):485-92. PubMed ID: 3928097
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  • 9. Pure XX gonadal dysgenesis in identical twins.
    Youlton R, Michelsen H, Be C, Cruz-Coke R.
    Clin Genet; 1982 Apr 15; 21(4):262-5. PubMed ID: 6809371
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  • 10. Absence of H-Y antigen in a case of sporadic pure gonadal dysgenesis.
    Boucekkine C, Benmiloud M, Himeur B, Chouiter A, Bachammar M.
    J Endocrinol Invest; 1984 Jun 15; 7(3):225-30. PubMed ID: 6432892
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  • 14. [Gonadal dysgenesis in own material].
    Gasińska-Drozdowska I, Goluda M, Hirowska-Tracz M, Roszyk-Rybińska A.
    Ginekol Pol; 1999 May 15; 70(5):363-6. PubMed ID: 10462982
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  • 16. 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
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  • 19. Mutation analysis of WNT4 gene in SRY negative 46,XX DSD patients with Mullerian agenesis and/or gonadal dysgenesis- An Indian study.
    Ragitha TS, Sunish KS, Gilvaz S, Daniel S, Varghese PR, Raj S, Francis J, Suresh Kumar R.
    Gene; 2023 Apr 20; 861():147236. PubMed ID: 36738897
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