BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

168 related articles for article (PubMed ID: 1237118)

  • 1. [Triploidy in the child. I. Study of phenotype. An observation of triploidy with mosaicism 46, XX/69, XXY].
    David M; Chambon A; Laurent C; Plauchu H; Lindner D; Rouchon A; de Peretti E; Genoud J; Jeune M
    Pediatrie; 1975; 30(3):281-98. PubMed ID: 1237118
    [No Abstract]   [Full Text] [Related]  

  • 2. [Triploidy (69,XXY) in a live born child].
    Keutel J; Dollmann A; Münster W
    Z Kinderheilkd; 1970; 109(2):104-17. PubMed ID: 5494203
    [No Abstract]   [Full Text] [Related]  

  • 3. [Complete triploidy in a liveborn premature (author's transl)].
    Rico S; Skinner C; Lechuga JL; Fernández E; Serrano J; Casanova M; Argemí J; López A; Castro JM
    An Esp Pediatr; 1980 Jan; 13(1):71-80. PubMed ID: 7189392
    [TBL] [Abstract][Full Text] [Related]  

  • 4. [Ring chromosomes in mosaicism 46, XY, Cr-46, XY].
    Ferrier S; Freund M; Grétillat A
    Arch Genet (Zur); 1973; 46(1):1-14. PubMed ID: 4731928
    [No Abstract]   [Full Text] [Related]  

  • 5. X-XY mosaicism with short y.
    Berger R; Relier JP; Salmon C; Minkowski A
    Clin Genet; 1974; 5(3):211-7. PubMed ID: 4134782
    [No Abstract]   [Full Text] [Related]  

  • 6. [Male pseudohermaphroditism. Management of etiological diagnosis. 1st part].
    Vague J; Guidon J
    Sem Hop; 1977 Oct; 53(36):1915-20. PubMed ID: 208157
    [No Abstract]   [Full Text] [Related]  

  • 7. Accuracy of perinatal diagnosis of 45,X/46,XY mosaicism and electronic consultation of affected parents.
    Kibar Y; Frimberger D; Kropp BP; Reiner W
    J Pediatr Urol; 2009 Aug; 5(4):274-8. PubMed ID: 19329364
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Multiple congenital defects associated with 45,XO-46,XYg- mosaicism.
    Surana RB; Hunt TM; Conen PE
    Am J Dis Child; 1973 Jul; 126(1):75-7. PubMed ID: 4723173
    [No Abstract]   [Full Text] [Related]  

  • 9. XO-XY gonadal dysgenesis and gonadoblastoma in childhood.
    Shabrov AV
    Obstet Gynecol; 1973 Apr; 41(4):536-41. PubMed ID: 4696971
    [No Abstract]   [Full Text] [Related]  

  • 10. [XX-XXX chromosomal mosaicism in an newborn with multiple malformations (author's transl)].
    Rosenkranz W; Kaloud H; Holzer S
    Padiatr Padol; 1971; 6(3):313-8. PubMed ID: 5164146
    [No Abstract]   [Full Text] [Related]  

  • 11. Presumptive 46,XX-46,XY-47,XXY mosaicism in a hermaphrodite.
    Chaudhuri A; Chatterjee SK; Sarkar S
    J Med Genet; 1971 Mar; 8(1):117-22. PubMed ID: 5098067
    [No Abstract]   [Full Text] [Related]  

  • 12. [A case of complete triploidy (69,XXY) in a premature infant. Presence of a clinical syndrome characteristic of this chromosome abnormality].
    Castel Y; Rivière D; Toudic L; Alix D; Leroy JP
    Ann Pediatr (Paris); 1976 Oct; 23(10):639-45. PubMed ID: 16106892
    [No Abstract]   [Full Text] [Related]  

  • 13. Autosomal/heterosomal mixoploids: a report on two patients, a female with a 45, Z/47,XX plus 21 and a male with A 45,X/47,XY, plus 21 chromosome constitution.
    Hustinx TW; Haar BG; Scheres JM; Rutten FJ
    Ann Genet; 1974 Dec; 17(4):225-34. PubMed ID: 4281287
    [No Abstract]   [Full Text] [Related]  

  • 14. Paucity of 47,XXX and 46,XX/47,XXX among routine diagnostic cytogenetic referrals.
    Bell J; Pearn J
    Med J Aust; 1983 Nov; 2(11):535-6. PubMed ID: 6633377
    [No Abstract]   [Full Text] [Related]  

  • 15. Kabuki syndrome in son and low grade mosaic 45,X/46,XX in mother.
    Van Hagen JM; Kwee ML; Madan K; Nieuwint AW; Pals G; ten Kate LP
    Genet Couns; 1996; 7(3):201-6. PubMed ID: 8897041
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Fetal gender: antenatal discrepancy between phenotype and genotype.
    Bretelle F; Salomon L; Senat MV; Vialard F; Albert M; Roume J; Ville Y
    Ultrasound Obstet Gynecol; 2002 Sep; 20(3):286-9. PubMed ID: 12230454
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Structural rearrangement of chromosome 1 and 46, XY-47, XXY mosaicism in a child with a disorder of sex differentiation.
    Zhukovskii MA; Dzenis IG
    Sov Genet; 1974 Jul; 8(7):932-6. PubMed ID: 4472605
    [No Abstract]   [Full Text] [Related]  

  • 18. A child with multiple congenital malformations and a 46,XX,t(Bq+;Dq-)-45,XX,-B,-D,+der(B),t(Bq+;Dq-) karyotype.
    Carnevale A; De los Cobos L
    J Med Genet; 1973 Dec; 10(4):376-9. PubMed ID: 4359604
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Triploid mosaicism in a 45,X/69,XXY infant.
    Quigley DI; McDonald MT; Krishnamuthy V; Kishnani PS; Lee MM; Haqq AM; Goodman BK
    Am J Med Genet A; 2005 Oct; 138A(2):171-4. PubMed ID: 16152633
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Mixed gonadal dysgenesis.
    Davidoff F; Federman DD
    Pediatrics; 1973 Nov; 52(5):725-42. PubMed ID: 4147604
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 9.