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.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

105 related articles for article (PubMed ID: 1745840)

  • 21. A novel Arg615Ser mutation of androgen receptor DNA-binding domain in three 46,XY sisters with complete androgen insensitivity syndrome and bilateral inguinal hernia.
    Sharma V; Singh R; Thangaraj K; Jyothy A
    Fertil Steril; 2011 Feb; 95(2):804.e19-21. PubMed ID: 20888558
    [TBL] [Abstract][Full Text] [Related]  

  • 22. A novel mutation (c.2735_2736delTC) in the androgen receptor gene in 46,XY females with complete androgen insensitivity syndrome in an Egyptian family.
    Mazen I; Soliman H; El-Gammal M; Torky A; Mekkawy M; Abdel-Hamid MS; Essawi M
    Horm Res Paediatr; 2014; 82(6):411-4. PubMed ID: 25034089
    [TBL] [Abstract][Full Text] [Related]  

  • 23. A seminoma case which occurred in a patient with familial testicular feminization syndrome.
    Kocak M; Yalvac S; Pata O; Turan H; Haberal A
    Acta Obstet Gynecol Scand; 2000 Oct; 79(10):890-1. PubMed ID: 11304976
    [No Abstract]   [Full Text] [Related]  

  • 24. [Swyer syndrome. Apropos of a new case of pure gonadal dysgenesis with Karyotype 46 XY].
    Cossard F; Saurel J; Berger-Pauquet M; Brun G
    J Gynecol Obstet Biol Reprod (Paris); 1984; 13(2):151-6. PubMed ID: 6736590
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Clinical and pathologic spectrum of 46,XY gonadal dysgenesis: its relevance to the understanding of sex differentiation.
    Berkovitz GD; Fechner PY; Zacur HW; Rock JA; Snyder HM; Migeon CJ; Perlman EJ
    Medicine (Baltimore); 1991 Nov; 70(6):375-83. PubMed ID: 1956279
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Genetic forms of hypogonadism in the male.
    Summitt RL
    Prog Med Genet; 1979; 3():1-72. PubMed ID: 392597
    [No Abstract]   [Full Text] [Related]  

  • 27. [Diagnosis and management of 46,XY mixed gonadal dysgenesis and disorder of sexual differentiation].
    Verkauskas G; Macianskyte D; Janciauskas D; Preiksa RT; Verkauskiene R; Jaubert F
    Medicina (Kaunas); 2009; 45(5):357-64. PubMed ID: 19535881
    [TBL] [Abstract][Full Text] [Related]  

  • 28. [XY type gonadal dysgenesis, trisomy X and variants].
    Kikuchi I; Takeuchi H; Kinoshita K
    Nihon Rinsho; 2004 Feb; 62(2):309-12. PubMed ID: 14968537
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Description and molecular analysis of SRY and AR genes in a patient with 46,XY pure gonadal dysgenesis (Swyer syndrome).
    Iliopoulos D; Volakakis N; Tsiga A; Rousso I; Voyiatzis N
    Ann Genet; 2004; 47(2):185-90. PubMed ID: 15183752
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Genetics of H-Y antigen and its gonad-specific receptor.
    Müller U
    Bibl Anat; 1983; 24():111-8. PubMed ID: 6342602
    [No Abstract]   [Full Text] [Related]  

  • 31. 46, XY female--a case report.
    Leow MK; Loh KC
    Ann Acad Med Singap; 2001 Jan; 30(1):71-5. PubMed ID: 11242631
    [TBL] [Abstract][Full Text] [Related]  

  • 32. [A Case of 46,XY pure gonadal dysgenesis with loss of the sex-determining region of Y chromosome].
    Yoon KH; Lee YJ
    Korean J Lab Med; 2008 Apr; 28(2):151-4. PubMed ID: 18458512
    [TBL] [Abstract][Full Text] [Related]  

  • 33. A mutation c.C2812T in the androgen receptor gene resulting in Pro817Leu substitution may affect dimerization of the androgen receptor and result in androgen insensitivity syndrome.
    Turek-Plewa J; Eckersdorf-Mastalerz A; Kaluzewski B; Helszer Z; Trzeciak WH
    Fertil Steril; 2006 Jun; 85(6):1822.e1-4. PubMed ID: 16759930
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Care of women with XY karyotype: a clinical practice guideline.
    Jorgensen PB; Kjartansdóttir KR; Fedder J
    Fertil Steril; 2010 Jun; 94(1):105-13. PubMed ID: 19361791
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Increased risk of gonadal malignancy and prophylactic gonadectomy: a study of 102 phenotypic female patients with Y chromosome or Y-derived sequences.
    Liu AX; Shi HY; Cai ZJ; Liu A; Zhang D; Huang HF; Jin HM
    Hum Reprod; 2014 Jul; 29(7):1413-9. PubMed ID: 24826988
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Mutations of androgen receptor gene in androgen insensitivity syndromes.
    Sultan C; Lumbroso S; Poujol N; Belon C; Boudon C; Lobaccaro JM
    J Steroid Biochem Mol Biol; 1993 Nov; 46(5):519-30. PubMed ID: 8240973
    [TBL] [Abstract][Full Text] [Related]  

  • 37. A frame shift mutation in the DNA-binding domain of the androgen receptor gene associated with complete androgen insensitivity, persistent müllerian structures, and germ cell tumors in dysgenetic gonads.
    Chen CP; Chen SR; Wang TY; Wang W; Hwu YM
    Fertil Steril; 1999 Jul; 72(1):170-3. PubMed ID: 10428170
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Report of a kindred with X-linked (or autosomal dominant sex-limited) 46,XY partial gonadal dysgenesis.
    Fechner PY; Marcantonio SM; Ogata T; Rosales TO; Smith KD; Goodfellow PN; Migeon CJ; Berkovitz GD
    J Clin Endocrinol Metab; 1993 May; 76(5):1248-53. PubMed ID: 8496317
    [TBL] [Abstract][Full Text] [Related]  

  • 39. A new familial syndrome of 46,XY gonadal dysgenesis with anomalies of ectodermal and mesodermal structures.
    Brosnan PG; Lewandowski RC; Toguri AG; Payer AF; Meyer WJ
    J Pediatr; 1980 Oct; 97(4):586-90. PubMed ID: 6158563
    [TBL] [Abstract][Full Text] [Related]  

  • 40. AN XY FEMALE WITH ABSENT GONADS AND VESTIGIAL PELVIC ORGANS.
    DEWHURST CJ; PAINE CG; BLANK CE
    J Obstet Gynaecol Br Commonw; 1963 Aug; 70():675-80. PubMed ID: 14078046
    [No Abstract]   [Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 6.