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 *

151 related articles for article (PubMed ID: 6604491)

  • 1. [Unusual chromosomal rearrangement. An autosomal telomeric translocation on a multicentury satellited Y (Yqs) chromosome].
    Genest P; Genest FB; Gagnon-Blais D
    Ann Genet; 1983; 26(2):86-90. PubMed ID: 6604491
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Origin and structure of a satellited Y chromosome.
    Martin Lucas MA; Pérez Castillo A; Abrisqueta JA
    Ann Genet; 1984; 27(3):184-6. PubMed ID: 6334485
    [TBL] [Abstract][Full Text] [Related]  

  • 3. E trisomy phenotype associated with small metacentric chromosome and a familial Y-22 translocation.
    Dumars KW; Fialko G; Larson E
    Birth Defects Orig Artic Ser; 1976; 12(5):97-104. PubMed ID: 953249
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Satellited Y chromosomes: structure, origin, and clinical significance.
    Schmid M; Haaf T; Solleder E; Schempp W; Leipoldt M; Heilbronner H
    Hum Genet; 1984; 67(1):72-85. PubMed ID: 6745929
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Prenatal diagnosis of two rare de novo structural aberrations of the Y chromosome: cytogenetic and molecular analysis.
    Velissariou V; Antoniadi T; Patsalis P; Christopoulou S; Hatzipouliou A; Donoghue J; Bakou K; Kaminopetros P; Athanassiou V; Petersen MB
    Prenat Diagn; 2001 Jun; 21(6):484-7. PubMed ID: 11438955
    [TBL] [Abstract][Full Text] [Related]  

  • 6. [Rare structural rearrangement of the Y chromosome (Yq-,S) in the family of a boy with a sex differentiation disorder].
    Verlinskaia DK; Kovaleva NV; Prozorova MV; Khitrikova LE
    Tsitologiia; 1983 Feb; 25(2):204-6. PubMed ID: 6134363
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Loss of the Y chromosomal PAR2-region in four familial cases of satellited Y chromosomes (Yqs).
    Kühl H; Röttger S; Heilbronner H; Enders H; Schempp W
    Chromosome Res; 2001; 9(3):215-22. PubMed ID: 11330396
    [TBL] [Abstract][Full Text] [Related]  

  • 8. [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]  

  • 9. Report of a family case of satellited Y chromosome associated with a severe oligoasthenoteratospermia. A review of the literature.
    Couturier-Turpin MH; Ingster O; Salat-Baroux J; Feldmann G
    Ann Genet; 1994; 37(4):200-6. PubMed ID: 7710256
    [TBL] [Abstract][Full Text] [Related]  

  • 10. 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]  

  • 11. Molecular cytogenetic characterization of three familial cases of satellited Y chromosomes.
    Wilkinson TA; Crolla JA
    Hum Genet; 1993 May; 91(4):389-91. PubMed ID: 8500794
    [TBL] [Abstract][Full Text] [Related]  

  • 12. De novo X;Y translocation associated with imperforate anus and retinal pigmentary abnormalities.
    Johnston K; Schonberg S; Littman V; Gregory T; Gelbart S; O'Donnell J; Cox DR
    Am J Med Genet; 1987 Jul; 27(3):603-11. PubMed ID: 3631132
    [TBL] [Abstract][Full Text] [Related]  

  • 13. A case of nondisjunction of chromosome 21 (47,X,Yqs,+21) in an Indian family with Yqs.
    Reddy KS; Thomas IM; Narayanan HS
    Ann Genet; 1984; 27(3):194-6. PubMed ID: 6334487
    [TBL] [Abstract][Full Text] [Related]  

  • 14. A cascade of chromosomal aberrations in three generations: a fragile 16q, an extra fragment and a rearranged 20.
    Côté GB; Papadakou-Lagoyanni S; Pantelakis S
    Ann Genet; 1978 Dec; 21(4):209-14. PubMed ID: 314256
    [TBL] [Abstract][Full Text] [Related]  

  • 15. [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]  

  • 16. Partial monosomy 22pter leads to q11 in a newborn with the clinical features of trisomy 13 syndrome.
    Back E; Stier R; Böhm N; Adlung A; Hameister H
    Ann Genet; 1980; 23(4):244-8. PubMed ID: 6971606
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Detection of t(X;Y) in 2 XX males using fluorescent in situ hybridization.
    Taiar N; Qumsiyeh MB; Croteau S; Rollet J; Benkhalifa M
    Ann Genet; 1995; 38(2):102-5. PubMed ID: 7486824
    [TBL] [Abstract][Full Text] [Related]  

  • 18. [Familial translocation 22/Y and partial autosomal trisomy in a young girl].
    Kessel E; Pfeiffer RA; Welling P
    J Genet Hum; 1979 Mar; 27(1):45-51. PubMed ID: 573310
    [TBL] [Abstract][Full Text] [Related]  

  • 19. A phenotypical male infant with 46,X,der(Y)t(X;Y)(?;p11) de novo.
    Govaerts LC; Draaisma JM; vd Blij-Philipsen M; Smeets DF
    Ann Genet; 1997; 40(1):41-4. PubMed ID: 9150849
    [No Abstract]   [Full Text] [Related]  

  • 20. Tandem Y/6 translocation with partial deletion 6 (p23----pter).
    Kelly PC; Blake WW; Davis JR
    Clin Genet; 1989 Sep; 36(3):204-7. PubMed ID: 2791334
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 8.