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 *

92 related articles for article (PubMed ID: 6977302)

  • 1. A new family with a satellited Y.
    Shabtai F; Eilam N; Elian E; Halbrecht I
    Ann Genet; 1981; 24(4):223-5. PubMed ID: 6977302
    [No Abstract]   [Full Text] [Related]  

  • 2. [A satellited Y chromosome].
    Genest P
    Ann Genet; 1978 Dec; 21(4):237-8. PubMed ID: 314263
    [TBL] [Abstract][Full Text] [Related]  

  • 3. [Satellited Y chromosome (Yqs) and nucleolar organizer occurring de novo].
    Turleau C; Chavin-Colin F; Seger J; Sorin M; Salet D; de Grouchy J
    Ann Genet; 1978 Dec; 21(4):239-42. PubMed ID: 314264
    [TBL] [Abstract][Full Text] [Related]  

  • 4. [Remarks on a satellited Y chromosome (author's transl)].
    Genest P
    Sem Hop; 1979 Apr 18-25; 55(15-16):799-800. PubMed ID: 227075
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Evaluation of satellited Y chromosome (Yqs) detected during prenatal diagnosis.
    Haddad BR; Huang Y; Wyandt H; Milunsky A
    Acta Obstet Gynecol Scand; 1997 Mar; 76(3):281-3. PubMed ID: 9093147
    [No Abstract]   [Full Text] [Related]  

  • 6. [Numerical and structural aberrations of human Y chromosome].
    Parcheta B
    Pol Tyg Lek; 1980 Apr; 35(15):543-6. PubMed ID: 6995959
    [No Abstract]   [Full Text] [Related]  

  • 7. Loss of the Y chromosome PAR2 region and additional rearrangements in two familial cases of satellited Y chromosomes: cytogenetic and molecular analysis.
    Velissariou V; Sismani C; Christopoulou S; Kaminopetros P; Hatzaki A; Evangelidou P; Koumbaris G; Bartsocas CS; Stylianidou G; Skordis N; Diakoumakos A; Patsalis PC
    Eur J Med Genet; 2007; 50(4):291-300. PubMed ID: 17584536
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Elucidation of the cytogenetic abnormality in a 4p- "phenocopy".
    Curry CJ; Ying KL; O'Lague P; Tsai J
    Birth Defects Orig Artic Ser; 1982; 18(3B):275-86. PubMed ID: 7139110
    [No Abstract]   [Full Text] [Related]  

  • 9. Cytogenetic polymorphism or Y/15 translocation in a black male with ambiguous genitalia.
    Verma RS; Dosik H; Jhaveri RC; Warman J
    J Genet Hum; 1978 Dec; 26(4):405-9. PubMed ID: 752070
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Facial asymmetries: problems in genetic counselling.
    Dodinval P
    J Genet Hum; 1979 Oct; 27(3):189-203. PubMed ID: 536738
    [TBL] [Abstract][Full Text] [Related]  

  • 11. [Attenuated phenotype of trisomy 4p by translocation t(X;4)(p21.2;p13)].
    Morichon-Delvallez N; Couturier J; Frison B
    Ann Genet; 1982; 25(4):246-8. PubMed ID: 6985016
    [TBL] [Abstract][Full Text] [Related]  

  • 12. [Observation of 7 cases of rare autosomal pathology. Trisomy 9p; monosomy 18q; ring 21; trisomy 6p; trisomy 2q 1-21 translocation].
    Fioretti G; Pagano L; Renda S; Festa B; Rinaldi A; Celona A; Casullo C; Stabile M; Cavaliere ML; Ventruto V
    Minerva Pediatr; 1980 Jun; 32(12):807-14. PubMed ID: 7464734
    [No Abstract]   [Full Text] [Related]  

  • 13. [Phenotype anomalies in subjects with balanced chromosome translocation. Presentation of 4 cases].
    Ventruto V; Festa B; Renda S; Stabile M; Rinaldi A; Rinaldi MM; Cavaliere ML; Lonardo F; Garofalo S
    Pathologica; 1983; 75 Suppl():258-61. PubMed ID: 6680428
    [No Abstract]   [Full Text] [Related]  

  • 14. [Trisomy 10p as a result of familial 10/22 translocation].
    Zergollern L; Begovic D; Muzinić D
    Acta Med Iugosl; 1980; 34(2):113-22. PubMed ID: 7405617
    [No Abstract]   [Full Text] [Related]  

  • 15. [Phenotypic disorders in balanced reciprocal translocation: karyotype 46,XY,rcp(13; 21)(q22; q22)].
    Badalian LO; Malygina NA; Gozman TV; Petrukhin AS; Mutovin GR
    Tsitol Genet; 1982; 16(2):17-21. PubMed ID: 7101445
    [TBL] [Abstract][Full Text] [Related]  

  • 16. [Proximal and distal partial trisomy 13 in the same family].
    Zergollern L; Begovic D; Hitrec V
    Acta Med Iugosl; 1980; 34(2):123-35. PubMed ID: 7405618
    [No Abstract]   [Full Text] [Related]  

  • 17. [Y chromosome variation in man].
    Brogger A; Urdal T; Larsen FB; Lavik NJ
    Tidsskr Nor Laegeforen; 1977 Aug; 97(22):1087-9. PubMed ID: 905986
    [No Abstract]   [Full Text] [Related]  

  • 18. Phenotype/karyotype correlations of Y chromosome aneuploidy with emphasis on structural aberrations in postnatally diagnosed cases.
    Hsu LY
    Am J Med Genet; 1994 Nov; 53(2):108-40. PubMed ID: 7856637
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Prenatal diagnosis of inherited satellited non-acrocentric chromosomes.
    Chen CP; Devriendt K; Chern SR; Lee CC; Wang W; Lin SP
    Prenat Diagn; 2000 May; 20(5):384-9. PubMed ID: 10820405
    [TBL] [Abstract][Full Text] [Related]  

  • 20. [Hereditary transmission for 300 years of a satellited Y chromosome in a family].
    Genest P
    Ann Genet; 1973 Mar; 16(1):35-8. PubMed ID: 4541807
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 5.