BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

242 related articles for article (PubMed ID: 15755052)

  • 21. Molecular cytogenetic analysis of a ring-Y infertile male patient.
    Carvalho FM; Wolfgramm EV; Degasperi I; Verbeno BM; Vianna BA; Chagas FF; Perroni AM; Paula F; Louro ID
    Genet Mol Res; 2007 Mar; 6(1):59-66. PubMed ID: 17469055
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Mosaic tetrasomy 9p case with the phenotype mimicking Klinefelter syndrome and hyporesponse of gonadotropin-stimulated testosterone production.
    Ogino W; Takeshima Y; Nishiyama A; Yagi M; Oka N; Matsuo M
    Kobe J Med Sci; 2007; 53(4):143-50. PubMed ID: 17932453
    [TBL] [Abstract][Full Text] [Related]  

  • 23. [46,XX karyotype males, based on a specific case].
    Tar A; Rácz K; Dobos M; Barbaux S; McElreavey K; Fellous M
    Orv Hetil; 1996 May; 137(20):1085-7. PubMed ID: 8657421
    [TBL] [Abstract][Full Text] [Related]  

  • 24. An infertile male with apparent 45,X turned out to have 45,X,der(Y)t(Y;13)(q11.2;q12),-13: clinicopathologic and cytogenomic studies.
    Cui YX; Xia XY; Pan LJ; Wang YH; Yao B; Huang YF
    Fertil Steril; 2007 Dec; 88(6):1676.e7-11. PubMed ID: 17482602
    [TBL] [Abstract][Full Text] [Related]  

  • 25. [The value of cytogenetic investigations in the differential diagnosis of abnormalities in sex differentation (author's transl)].
    Von Gardó S; Papp Z
    Wien Klin Wochenschr; 1975 Jan; 87(2):44-7. PubMed ID: 1136506
    [TBL] [Abstract][Full Text] [Related]  

  • 26. [Rudimentary uterus in testicular feminization (author's transl)].
    Dapunt O; Platzer W; Gleispach H; Millonig-Ganner B
    Wien Klin Wochenschr; 1975 Sep; 87(16):498-506. PubMed ID: 1241635
    [TBL] [Abstract][Full Text] [Related]  

  • 27. X chromosomal abnormalities in Indian adolescent girls.
    Ganguly BB; Sahni S
    Teratog Carcinog Mutagen; 2003; Suppl 1():245-53. PubMed ID: 12616615
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Testicular feminization syndrome diagnosed in an elderly patient at surgery. A case report.
    Monaco A; La Brocca A; Verna C; Moncelli G; Berardengo E; Bollito E
    Panminerva Med; 1996 Sep; 38(3):193-8. PubMed ID: 9009687
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Extragonadal germ cell tumors are often associated with Klinefelter syndrome.
    Aguirre D; Nieto K; Lazos M; Peña YR; Palma I; Kofman-Alfaro S; Queipo G
    Hum Pathol; 2006 Apr; 37(4):477-80. PubMed ID: 16564924
    [TBL] [Abstract][Full Text] [Related]  

  • 30. [The results of cytogenetic and molecular genetic examinations in 35 couples with primary sterility].
    Pasińska M; Haus O; Skonieczka K; Slezak R; Midro AT; Stasiewicz-Jarocka B; Szczepaniak M; Adamczak R; Marcinkowska A; Bartusiak K
    Wiad Lek; 2006; 59(1-2):38-43. PubMed ID: 16646290
    [TBL] [Abstract][Full Text] [Related]  

  • 31. [A case of testicular feminization].
    Araki T; Hori N; Arima K; Sugimura Y; Tochigi H; Kawamura J
    Hinyokika Kiyo; 1988 Mar; 34(3):521-3. PubMed ID: 3133933
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Pseudodicentric 22;Y translocation transmitted through four generations of a large family without phenotypic repercussion.
    Morales C; Soler A; Bruguera J; Madrigal I; Alsius M; Obon M; Margarit E; Sánchez A
    Cytogenet Genome Res; 2007; 116(4):319-23. PubMed ID: 17431332
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Identification of a novel mutation in the SRY gene in a 46, XY female patient.
    Salehi LB; Scarciolla O; Vanni GF; Nardone AM; Frajese G; Novelli G; Stuppia L
    Eur J Med Genet; 2006; 49(6):494-8. PubMed ID: 16675314
    [TBL] [Abstract][Full Text] [Related]  

  • 34. A simple screening method for detection of Klinefelter syndrome and other X-chromosome aneuploidies based on copy number of the androgen receptor gene.
    Ottesen AM; Garn ID; Aksglaede L; Juul A; Rajpert-De Meyts E
    Mol Hum Reprod; 2007 Oct; 13(10):745-50. PubMed ID: 17720778
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Ontogeny and cellular localization of SRY transcripts in the human testes and its detection in spermatozoa.
    Modi D; Shah C; Sachdeva G; Gadkar S; Bhartiya D; Puri C
    Reproduction; 2005 Nov; 130(5):603-13. PubMed ID: 16264091
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Testicular feminization syndrome.
    Olson GP
    Nurse Pract; 1988 Feb; 13(2):27-32. PubMed ID: 3344095
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Clinical, hormonal and cytogenetic evaluation of 46,XX males and review of the literature.
    Ergun-Longmire B; Vinci G; Alonso L; Matthew S; Tansil S; Lin-Su K; McElreavey K; New MI
    J Pediatr Endocrinol Metab; 2005 Aug; 18(8):739-48. PubMed ID: 16200839
    [TBL] [Abstract][Full Text] [Related]  

  • 38. SRY-negative 46,XX male with normal genitals, complete masculinization and infertility.
    Rajender S; Rajani V; Gupta NJ; Chakravarty B; Singh L; Thangaraj K
    Mol Hum Reprod; 2006 May; 12(5):341-6. PubMed ID: 16556678
    [TBL] [Abstract][Full Text] [Related]  

  • 39. [Marker chromosome analysis in Chinese patients with Turner syndrome by fluorescence in situ hybridization].
    Liang Y; Luo XP
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2005 Aug; 22(4):435-7. PubMed ID: 16086285
    [TBL] [Abstract][Full Text] [Related]  

  • 40. [Fluorescence analysis of 46, XYq plus karyotype in a case of testicular feminization syndrome].
    Limon J; Sylwestrowicz W; Emerich J
    Endokrynol Pol; 1974; 25(1):1-7. PubMed ID: 4848780
    [No Abstract]   [Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 13.