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 *

114 related articles for article (PubMed ID: 613693)

  • 21. [Gonadal dysgenesis in a mother and her daughter (author's transl)].
    Riviere L; Serville F; Schmitt B; Roger P
    Ann Endocrinol (Paris); 1979; 40(4):427-8. PubMed ID: 518023
    [TBL] [Abstract][Full Text] [Related]  

  • 22. [Turner syndrome. Cytogenetic analysis of 165 patients with Turner syndrome. 1st report].
    Vignetti P; Brinchi V; Bruni L; Rizzuti A; Tarani L; Tozzi MC
    Minerva Pediatr; 1990; 42(1-2):25-7. PubMed ID: 2336052
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Seminoma in a postmenopausal woman with a Y;15 translocation in peripheral blood lymphocytes and a t(Y;15)/45,X Turner mosaic pattern in skin fibroblasts.
    Hoshi N; Fujita M; Mikuni M; Fujino T; Okuyama K; Handa Y; Yamada H; Sagawa T; Hareyama H; Nakahori Y; Fujieda K; Kant JA; Nagashima K; Fujimoto S
    J Med Genet; 1998 Oct; 35(10):852-6. PubMed ID: 9783712
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Familial Turner syndrome with an X;Y translocation mosaicism: implications for genetic counseling.
    Portnoï MF; Chantot-Bastaraud S; Christin-Maitre S; Carbonne B; Beaujard MP; Keren B; Lévy J; Dommergues M; Cabrol S; Hyon C; Siffroi JP
    Eur J Med Genet; 2012 Nov; 55(11):635-40. PubMed ID: 22809487
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Isodicentric X chromosome in a woman with characteristics of gonadal dysgenesis.
    Laća Z; Ivanović M; Dramusić V; Morić-Petrović S
    Hum Genet; 1979 Jun; 49(2):237-41. PubMed ID: 468255
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Prenatal diagnosis of 45,X and 45,X mosaicism: the need for thorough cytogenetic and clinical evaluations.
    Huang B; Thangavelu M; Bhatt S; J Sandlin C; Wang S
    Prenat Diagn; 2002 Feb; 22(2):105-10. PubMed ID: 11857613
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Detection of cryptic Y chromosome mosaicism by coamplification PCR with archived cytogenetic slides of suspected Turner syndrome.
    Kim JW; Cho EH; Kim YM; Kim JM; Han JY; Park SY
    Exp Mol Med; 2000 Mar; 32(1):38-41. PubMed ID: 10762060
    [TBL] [Abstract][Full Text] [Related]  

  • 28. [Cytogenetic studies in primary amenorrhea].
    Baron J; Warenik-Szymankiewicz A
    Zentralbl Gynakol; 1975; 97(11):649-55. PubMed ID: 1189755
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Turner syndrome with rare karyotypes.
    Boczkowski K; Mikkelsen M; Poulsen H
    Clin Genet; 1978 May; 13(5):409-14. PubMed ID: 657581
    [TBL] [Abstract][Full Text] [Related]  

  • 30. [45,X/46, XYnf/47, XYnfYnf/46, X, dic (Ynf) (q12) mosaicism in a female patient with gonadal dysgenesis and the stigmata of Turner's syndrome].
    Gil R; Galán F; López-Ginés C; Gregori-Romero M; Millet A; Pellín A; Llombart-Bosch A
    Rev Clin Esp; 1991 Jun; 189(1):23-5. PubMed ID: 1924922
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Multiple cytogenetic methods used to identify a new structural rearrangement of the human X chromosome.
    de la Chapelle A; Grönman P; Latt SA
    Cytogenet Cell Genet; 1978; 20(1-6):204-12. PubMed ID: 348409
    [TBL] [Abstract][Full Text] [Related]  

  • 32. 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]  

  • 33. Discordant phenotypes and 45,X/46,X,idic(Y).
    Kelly TE; Franko JB; Rogol A; Golden WL
    J Med Genet; 1998 Oct; 35(10):862-4. PubMed ID: 9783714
    [TBL] [Abstract][Full Text] [Related]  

  • 34. A Turner-like phenotype in a girl with an isodicentric fluorescent Y chromosome mosaicism.
    Bergendi E; Plöchl E; Vlasak I; Rittinger O; Muss W
    Klin Padiatr; 1997; 209(3):133-6. PubMed ID: 9183775
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Turner phenotype in mother and daughter.
    Muasher S; Baramki TA; Diggs ES
    Obstet Gynecol; 1980 Dec; 56(6):752-6. PubMed ID: 7443121
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Turner syndrome patients with a ring X chromosome.
    Berkovitz G; Stamberg J; Plotnick LP; Lanes R
    Clin Genet; 1983 Jun; 23(6):447-53. PubMed ID: 6883789
    [TBL] [Abstract][Full Text] [Related]  

  • 37. A study of 45,X/46,XX mosaicism in Turner syndrome females: a novel primer pair for the (CAG)n repeat within the androgen receptor gene.
    Leonova J; Hanson C
    Hereditas; 1999; 131(2):87-92. PubMed ID: 10680293
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Cytogenetic and molecular-cytogenetic studies of Rett syndrome (RTT): a retrospective analysis of a Russian cohort of RTT patients (the investigation of 57 girls and three boys).
    Vorsanova SG; Yurov YB; Ulas VY; Demidova IA; Sharonin VO; Kolotii AD; Gorbatchevskaia NL; Beresheva AK; Soloviev IV
    Brain Dev; 2001 Dec; 23 Suppl 1():S196-201. PubMed ID: 11738872
    [TBL] [Abstract][Full Text] [Related]  

  • 39. 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]  

  • 40. Mosaicism in 45,X Turner syndrome: does survival in early pregnancy depend on the presence of two sex chromosomes?
    Held KR; Kerber S; Kaminsky E; Singh S; Goetz P; Seemanova E; Goedde HW
    Hum Genet; 1992 Jan; 88(3):288-94. PubMed ID: 1733830
    [TBL] [Abstract][Full Text] [Related]  

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