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 *

616 related articles for article (PubMed ID: 4281287)

  • 1. 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]  

  • 2. [Double aneuploidy: 46,XX-45,XO-47,XX,G+. Case report].
    Grosse KP; Hopfengärtner F; Schwanitz G
    Humangenetik; 1971; 13(4):333-7. PubMed ID: 4257570
    [No Abstract]   [Full Text] [Related]  

  • 3. [Indications for chromosome analysis from the pediatric viewpoint].
    Steinbicker V; Braun HS; Hemke G; Euchler HB
    Kinderarztl Prax; 1973 Feb; 41(2):91-8. PubMed ID: 4267824
    [No Abstract]   [Full Text] [Related]  

  • 4. [Dermatoglyphics in medicine].
    Sharets IuD
    Vestn Akad Med Nauk SSSR; 1973; 28(7):61-9. PubMed ID: 4274403
    [No Abstract]   [Full Text] [Related]  

  • 5. [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]  

  • 6. 46,XY-47,XY,C+ mosaicism in a male infant with multiple anomalies.
    Oikawa K; Kajii T; Shimba H; Sasaki M
    Ann Genet; 1969 Jun; 12(2):102-6. PubMed ID: 5308379
    [No Abstract]   [Full Text] [Related]  

  • 7. Cytogenetic abnormalities in orthopedic patients.
    Cowell HR; Clark CE
    Clin Orthop Relat Res; 1978 Sep; (135):4-14. PubMed ID: 152176
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Sex chromosome mosaicism of X/XY or X/XY/XYY.
    Wilson MG; Ebbin AJ; Shinno NW; Towner JW
    Birth Defects Orig Artic Ser; 1975; 11(5):255-66. PubMed ID: 1218222
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Double aneuploidy in three Egyptian patients: Down-Turner and Down-Klinefelter syndromes.
    Zaki MS; Kamel AA; El-Ruby M
    Genet Couns; 2005; 16(4):393-402. PubMed ID: 16440882
    [TBL] [Abstract][Full Text] [Related]  

  • 10. [Cytogenetic study of 257 mentally deficient patients in psychiatric hospitals].
    Bourgeois M; Bénézech M; Tournier-Zerbid N; Constant-Boy M; Benazet-Rissou J
    Ann Med Psychol (Paris); 1975 Nov; 2(4):756-82. PubMed ID: 135524
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Human chromosome analysis.
    Centerwall WR; Murdoch JL
    Am Fam Physician; 1975 Apr; 11(4):76-89. PubMed ID: 123406
    [No Abstract]   [Full Text] [Related]  

  • 12. Partial trisomy 15 in a male with severe psychomotor retardation (48, XY, + 15q -, + mar(15)).
    Voss R; Lerer I; Maftzir G; Sheinis M; Cohen MM
    Am J Med Genet; 1982 Jun; 12(2):131-9. PubMed ID: 7102721
    [TBL] [Abstract][Full Text] [Related]  

  • 13. [Cytogenetic survey in 105 psychiatric hospital patients].
    Bourgeois M; Benezech M; Limousin G
    Ann Med Psychol (Paris); 1974 Dec; 2(5):734-43. PubMed ID: 4458595
    [No Abstract]   [Full Text] [Related]  

  • 14. Double monosomy mosaicism (45,X-45, XX,21-) in a retarded child with multiple congenital malformations.
    Weber FM; Sparkes RS; Muller H
    Cytogenetics; 1971; 10(6):404-12. PubMed ID: 5146417
    [No Abstract]   [Full Text] [Related]  

  • 15. Monosomy 21: a possible stepwise evolution of the karyotype.
    Abeliovich D; Carmi R; Karplus M; Bar-Ziv J; Cohen MM
    Am J Med Genet; 1979; 4(3):279-86. PubMed ID: 574719
    [TBL] [Abstract][Full Text] [Related]  

  • 16. [Monosomy 21 with mosaicism 45,XX,21--46,XX,21 pi].
    Emberger JM; Rey J; Rieu D; Dossa D; Bonnet H; Jean R
    Arch Fr Pediatr; 1970; 27(10):1069-79. PubMed ID: 5495707
    [No Abstract]   [Full Text] [Related]  

  • 17. [Clinical chromosome studies].
    Ganner E
    Wien Klin Wochenschr; 1968 Oct; 80(41):755-7 passim. PubMed ID: 4236317
    [No Abstract]   [Full Text] [Related]  

  • 18. [Familial translocation t(4;22) (p11;p12) and trisomy 4p in 2 sisters].
    Giovannelli G; Forabosco A; Dutrillaux B
    Ann Genet; 1974 Jun; 17(2):119-24. PubMed ID: 4547939
    [No Abstract]   [Full Text] [Related]  

  • 19. Autosomal chromosome aberrations in ophthalmology.
    Francois J
    Int Ophthalmol Clin; 1968; 8(4):839-910. PubMed ID: 4244691
    [No Abstract]   [Full Text] [Related]  

  • 20. [Partial 7q trisomy].
    Serville F; Broustet A; Sandler B; Bourdeau MJ; Leloup M
    Ann Genet; 1975 Mar; 18(1):67-70. PubMed ID: 1080040
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 31.