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: 4765202)

  • 21. Double autosomal chromosomal aberration (3p trisomy/9p monosomy) and sex-reversal.
    Fryns JP; Kleczkowska A; Casaer P; van den Berghe H
    Ann Genet; 1986; 29(1):49-52. PubMed ID: 3487277
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Relationship between anomalies of phenotype and karyotype in human embryogenesis.
    Kuliev AM
    Sov Genet; 1974 Jul; 8(7):910-20. PubMed ID: 4424716
    [No Abstract]   [Full Text] [Related]  

  • 23. [Partial monosomy of a C group chromosome (Cp-)].
    Laurent C; Nivelon A; Hartman E; Guerrier G
    Ann Genet; 1968 Dec; 11(4):231-5. PubMed ID: 5306365
    [No Abstract]   [Full Text] [Related]  

  • 24. [Chromosome aberrations in abortions].
    Boué JG; Boué A; Lazar P
    Ann Genet; 1967 Dec; 10(4):179-87. PubMed ID: 5301690
    [No Abstract]   [Full Text] [Related]  

  • 25. [C-G translocation: karyotype 46, XY,t(Cq-; Gq+): parents 46, XX and 46, XY].
    Lambotte C; Carlier G; Frederic J; Keutgen J
    Acta Paediatr Belg; 1971; 25(2):119-26. PubMed ID: 5565831
    [No Abstract]   [Full Text] [Related]  

  • 26. Fetal chromosome analysis after transcervical placental biopsies during early pregnancy.
    Kullander S; Sandahl B
    Acta Obstet Gynecol Scand; 1973; 52(4):355-9. PubMed ID: 4766093
    [No Abstract]   [Full Text] [Related]  

  • 27. Deletion of the short arm of chromosome No. 10.
    Shokeir MH; Ray M; Hamerton JL; Bauder F; O'Brien H
    J Med Genet; 1975 Mar; 12(1):99-103. PubMed ID: 47396
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Trisomy/partial monosomy mosaicism of no. 13 pair [46, XX,--13, + rob(13q13q)/46, XX, r(13) (pllq34)].
    Oka S; Nakagome Y; Teramura F; Hosono F; Katumata M
    Jinrui Idengaku Zasshi; 1977 Sep; 22(2-3):73-8. PubMed ID: 604564
    [No Abstract]   [Full Text] [Related]  

  • 29. X chromatin and chromosome examination in aged women.
    Yen FF; Matsuyama SS; Jarvik LF
    Mech Ageing Dev; 1981 May; 16(1):55-60. PubMed ID: 7195966
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Congenital malformations associated with a ring 4 chromosome.
    Carter R; Baker E; Hayman D
    J Med Genet; 1969 Jun; 6(2):224-7. PubMed ID: 5801472
    [No Abstract]   [Full Text] [Related]  

  • 31. Monosomy of chromosome No. 22. A case report.
    DeCicco F; Steele MW; Pan S; Park SC
    J Pediatr; 1973 Nov; 83(5):836-8. PubMed ID: 4126387
    [No Abstract]   [Full Text] [Related]  

  • 32. "Pure" monosomy 21 pter leads to q21 in a girl born to a couple 46,XX,t(14;21)(p12;q22) and 46,XY,t(5;18)(q32;q22).
    Rivera H; Rivas F; Plascencia L; Cantú JM
    Ann Genet; 1983; 26(4):234-7. PubMed ID: 6607704
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Familial occurrence of congenital malformations and ring chromosome (46,XX,Cr).
    Gacs G; Schuler D; Sellyei M
    J Med Genet; 1970 Jun; 7(2):177-9. PubMed ID: 5534843
    [No Abstract]   [Full Text] [Related]  

  • 34. Fetal anomalies associated with an inversion duplication 13 chromosome.
    Rijhsinghani AG; Hruban RH; Stetten G
    Obstet Gynecol; 1988 Jun; 71(6 Pt 2):991-4. PubMed ID: 3287254
    [TBL] [Abstract][Full Text] [Related]  

  • 35. A 46,XX,t(Cp+;Cq-) translocation in a girl with multiple congenital anomalies and in her phenotypically normal father 46,XY,t(Cq+;Cq-).
    Bargman GJ; Neu RL; Powers HO; Gardner LI
    J Med Genet; 1970 Mar; 7(1):77-80. PubMed ID: 5480968
    [No Abstract]   [Full Text] [Related]  

  • 36. Ring chromosomes in two infants with congenital malformations.
    Varela MA; Sternberg WH
    J Med Genet; 1969 Sep; 6(3):334-41. PubMed ID: 5345107
    [No Abstract]   [Full Text] [Related]  

  • 37. [9p monosomy. About a new case. Clinical and cytogenetic study (author's transl)].
    Lajarrige C; Bouquier JJ; Ronayette D; Tchertoff C; Faugeras C; Barthe D; Laleu J
    Ann Pediatr (Paris); 1979 Nov; 26(9):631-6. PubMed ID: 555637
    [No Abstract]   [Full Text] [Related]  

  • 38. Fetoplacental cytogenetic discrepancy in a pregnancy with fetal mosaic tetrasomy 12p and Pallister-Killian syndrome detected by amniocentesis.
    Chen CP; Wang LK; Chern SR; Wu PS; Chen SW; Lai ST; Chuang TY; Chen LF; Wang W
    Taiwan J Obstet Gynecol; 2017 Dec; 56(6):852-856. PubMed ID: 29241934
    [TBL] [Abstract][Full Text] [Related]  

  • 39. [Trisomy of group C (47, XX, C+)].
    Emberger JM; Rey J; Rieu D; Dossa D; Bonnet H; Jean R
    Arch Fr Pediatr; 1970; 27(10):1081-8. PubMed ID: 5495708
    [No Abstract]   [Full Text] [Related]  

  • 40. A new case of the trisomy 9P syndrome. Report of a patient with unusual chromosome findings (46,XX/47,XX, + i (9p) and a peculiar congenital heart defect.
    Orye E; Verhaaren H; Van Egmond H; Devloo-Blancquaert A
    Clin Genet; 1975 Feb; 7(2):134-43. PubMed ID: 1132161
    [TBL] [Abstract][Full Text] [Related]  

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