BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

169 related articles for article (PubMed ID: 18555994)

  • 41. Uniform testicular maturation arrest: a unique subset of men with nonobstructive azoospermia.
    Hung AJ; King P; Schlegel PN
    J Urol; 2007 Aug; 178(2):608-12; discussion 612. PubMed ID: 17570432
    [TBL] [Abstract][Full Text] [Related]  

  • 42. Clinical characterization of 42 oligospermic or azoospermic men with microdeletion of the AZFc region of the Y chromosome, and of 18 children conceived via ICSI.
    Oates RD; Silber S; Brown LG; Page DC
    Hum Reprod; 2002 Nov; 17(11):2813-24. PubMed ID: 12407032
    [TBL] [Abstract][Full Text] [Related]  

  • 43. A case of agonadism associated with y-chromosome rearrangement: cytogenetic and molecular studies.
    Cui YX; Shi YC; Liu Q; Xia XY; Lu HY; Shao HF; Jia L; Yao B; Ge YF; Li XJ; Huang YF
    J Androl; 2009; 30(6):650-4. PubMed ID: 19617372
    [TBL] [Abstract][Full Text] [Related]  

  • 44. 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; 31(7):611-5. PubMed ID: 3091820
    [TBL] [Abstract][Full Text] [Related]  

  • 45. Cytogenetic and molecular analysis of male infertility: Y chromosome deletion during nonobstructive azoospermia and severe oligozoospermia.
    Dada R; Gupta NP; Kucheria K
    Cell Biochem Biophys; 2006; 44(1):171-7. PubMed ID: 16456245
    [TBL] [Abstract][Full Text] [Related]  

  • 46. Intracytoplasmic sperm injection (ICSI) with transmission of a ring(Y) chromosome and ovotesticular disorder of sex development in offspring.
    Spinner NB; Saitta SC; Delaney DP; Colliton R; Zderic SA; Ruchelli E; Zackai E; Kolon TF
    Am J Med Genet A; 2008 Jul; 146A(14):1828-31. PubMed ID: 18553511
    [TBL] [Abstract][Full Text] [Related]  

  • 47. Sex determination and sex reversal: genotype, phenotype, dogma and semantics.
    Mittwoch U
    Hum Genet; 1992 Jul; 89(5):467-79. PubMed ID: 1634224
    [TBL] [Abstract][Full Text] [Related]  

  • 48. A Mixed Gonadal Dysgenesis in an 19 Year Old Girl with Ambigous Genitalia: A Case Report.
    Hardigaloeh AT; Tarigan TJE; Yunir E; Sumapradja K; Agiananda F; Ariani Y; Marzuki NS; Wahyudi I; Lisnawati L
    Acta Med Indones; 2023 Oct; 55(4):460-464. PubMed ID: 38213048
    [TBL] [Abstract][Full Text] [Related]  

  • 49. The spectrum of 45,X/46,XY mosaicism in Taiwanese children: The experience of a single center.
    Huang YC; Lee CT; Wu MZ; Liu SY; Tung YC; Ho HN; Tsai WY
    J Formos Med Assoc; 2019 Jan; 118(1 Pt 3):450-456. PubMed ID: 30017534
    [TBL] [Abstract][Full Text] [Related]  

  • 50. Multicenter study of genetic abnormalities associated with severe oligospermia and non-obstructive azoospermia.
    Xie C; Chen X; Liu Y; Wu Z; Ping P
    J Int Med Res; 2018 Jan; 46(1):107-114. PubMed ID: 28730893
    [TBL] [Abstract][Full Text] [Related]  

  • 51. Testicular gene expression in cryptorchid boys at risk of azoospermia.
    Hadziselimovic F; Hadziselimovic NO; Demougin P; Oakeley EJ
    Sex Dev; 2011; 5(2):49-59. PubMed ID: 21412036
    [TBL] [Abstract][Full Text] [Related]  

  • 52. Clinical but Not Histological Outcomes in Males With 45,X/46,XY Mosaicism Vary Depending on Reason for Diagnosis.
    Ljubicic ML; Jørgensen A; Acerini C; Andrade J; Balsamo A; Bertelloni S; Cools M; Cuccaro RT; Darendeliler F; Flück CE; Grinspon RP; Maciel-Guerra A; Guran T; Hannema SE; Lucas-Herald AK; Hiort O; Holterhus PM; Lichiardopol C; Looijenga LHJ; Ortolano R; Riedl S; Ahmed SF; Juul A
    J Clin Endocrinol Metab; 2019 Oct; 104(10):4366-4381. PubMed ID: 31127831
    [TBL] [Abstract][Full Text] [Related]  

  • 53. [Y chromosome microdeletions, chromosome karyotypes and reproductive hormones in patients with azoospermia and severe oligozoospermia].
    Liu CL; Wu XY; Qiu HQ; Shao SS; Zhu YR; Li XR
    Zhonghua Nan Ke Xue; 2013 Oct; 19(10):890-5. PubMed ID: 24218941
    [TBL] [Abstract][Full Text] [Related]  

  • 54. Genetic mutations and somatic anomalies in association with 46,XY gonadal dysgenesis.
    Bastian C; Muller JB; Lortat-Jacob S; Nihoul-Fékété C; Bignon-Topalovic J; McElreavey K; Bashamboo A; Brauner R
    Fertil Steril; 2015 May; 103(5):1297-304. PubMed ID: 25813279
    [TBL] [Abstract][Full Text] [Related]  

  • 55. Correlation of genetic results with testicular histology, hormones and sperm retrieval in nonobstructive azoospermia patients with testis biopsy.
    Liu W; Gao X; Ma G; Yan L; Chen T; Li T; Yu RM; Ma JL
    Andrologia; 2017 Sep; 49(7):. PubMed ID: 27921326
    [TBL] [Abstract][Full Text] [Related]  

  • 56. [A molecular analysis of females with 46,XY or 47, XYY karyotype].
    Shan X
    Zhongguo Yi Xue Ke Xue Yuan Xue Bao; 1992 Feb; 14(1):27-32. PubMed ID: 1534280
    [TBL] [Abstract][Full Text] [Related]  

  • 57. [Mixed gonadal dysgenesis combined with gonadoblastoma].
    Batashki I; Delev P; Pancheva S; Markova D; Milchev N
    Akush Ginekol (Sofiia); 2009; 48(3):51-3. PubMed ID: 20198767
    [TBL] [Abstract][Full Text] [Related]  

  • 58. [Y chromosome structural abnormalities and Turner's syndrome].
    Ravel C; Siffroi JP
    Gynecol Obstet Fertil; 2009 Jun; 37(6):511-8. PubMed ID: 19464936
    [TBL] [Abstract][Full Text] [Related]  

  • 59. 46,XX males: a case series based on clinical and genetics evaluation.
    Mohammadpour Lashkari F; Totonchi M; Zamanian MR; Mansouri Z; Sadighi Gilani MA; Sabbaghian M; Mohseni Meybodi A
    Andrologia; 2017 Sep; 49(7):. PubMed ID: 27882599
    [TBL] [Abstract][Full Text] [Related]  

  • 60. Mixed gonadal dysgenesis in a child with isodicentric Y chromosome: Does the relative proportion of the 45,X line really matter?
    Shinawi M; Cain MP; Vanderbrink BA; Grignon DJ; Mensing D; Cooper ML; Bader P; Cheung SW
    Am J Med Genet A; 2010 Jul; 152A(7):1832-7. PubMed ID: 20583182
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 9.