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 *

120 related articles for article (PubMed ID: 10910537)

  • 1. Study of human Y chromosome polymorphism in Taiwan.
    Hou JW; Wang TR
    Acta Paediatr Taiwan; 1999; 40(5):302-4. PubMed ID: 10910537
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Chromosomal polymorphisms of 1, 9, 16, and Y in 4 major ethnic groups: a large prenatal study.
    Hsu LY; Benn PA; Tannenbaum HL; Perlis TE; Carlson AD
    Am J Med Genet; 1987 Jan; 26(1):95-101. PubMed ID: 3812584
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Chromosomal variants in mentally retarded and normal men.
    Soudek D; Sroka H
    Clin Genet; 1979 Aug; 16(2):109-16. PubMed ID: 477019
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Molecular characterisation of a mosaicism with a complex chromosome rearrangement: evidence for coincident chromosome healing by telomere capture and neo-telomere formation.
    Chabchoub E; Rodríguez L; Galán E; Mansilla E; Martínez-Fernandez ML; Martínez-Frías ML; Fryns JP; Vermeesch JR
    J Med Genet; 2007 Apr; 44(4):250-6. PubMed ID: 17172463
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Three cases with rare interstitial rearrangements of chromosome 1 characterized by multicolor banding.
    Polityko A; Starke H; Rumyantseva N; Claussen U; Liehr T; Raskin S
    Cytogenet Genome Res; 2005; 111(2):171-4. PubMed ID: 16103660
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Heterogeneity of pericentric inversions of the human y chromosome.
    Knebel S; Pasantes JJ; Thi DA; Schaller F; Schempp W
    Cytogenet Genome Res; 2011; 132(4):219-26. PubMed ID: 21307635
    [TBL] [Abstract][Full Text] [Related]  

  • 7. A dysmorphic newborn with 45,X,der(1)inv(1)(p13;qter)t(Y;1)(pter-->q11;p13),-Y de novo karyotype.
    Tatar A; Oztas S; Yakut T; Ors R
    Genet Couns; 2005; 16(2):173-7. PubMed ID: 16080298
    [TBL] [Abstract][Full Text] [Related]  

  • 8. [Frequency of chromosome variants in human populations].
    Kuleshov NP; Kulieva LM
    Genetika; 1979; 15(3):745-51. PubMed ID: 160358
    [TBL] [Abstract][Full Text] [Related]  

  • 9. [Characterization of marker chromosomes using molecular cytogenetic methods in patients with mental retardation and congenital malformations].
    Bocian E; Nowakowska B; Obersztyn E; Borg K; Chudoba I; Kostyk E; Kruczek A; Pietrzyk J; Mazurczak T
    Med Wieku Rozwoj; 2006; 10(1 Pt 2):211-25. PubMed ID: 17028390
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Fifty probands with extra structurally abnormal chromosomes characterized by fluorescence in situ hybridization.
    Blennow E; Nielsen KB; Telenius H; Carter NP; Kristoffersson U; Holmberg E; Gillberg C; Nordenskjöld M
    Am J Med Genet; 1995 Jan; 55(1):85-94. PubMed ID: 7702104
    [TBL] [Abstract][Full Text] [Related]  

  • 11. [Sperm-fluorescence in situ hybridization analysis in patients with pericentric inversions of Y chromosome].
    Luo YQ; Qian YL; Lu HM; Xu CM; Jin F
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2009 Feb; 26(1):54-6. PubMed ID: 19199252
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Functional disomy of Xp22-pter in three males carrying a portion of Xp translocated to Yq.
    Bardoni B; Floridia G; Guioli S; Peverali G; Anichini C; Cisternino M; Casalone R; Danesino C; Fraccaro M; Zuffardi O
    Hum Genet; 1993 May; 91(4):333-8. PubMed ID: 8099057
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Reproductive failure in a carrier of inv dupl l(q21.4----q12).
    Toncheva D; Genkova P; Tzoneva M; Lozanova T; Angelova E; Mitreva B
    Acta Paediatr Hung; 1986; 27(1):61-6. PubMed ID: 3730184
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Variability of DA/DAPI and C heterochromatic regions: a population study.
    Tofanelli S; Stanyon R; Agostini M; Franceschi MG; Paoli G
    Hum Biol; 1993 Aug; 65(4):635-46. PubMed ID: 7802857
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Array-CGH characterization of a de novo t(X;Y)(p22;q11) in a female with short stature and mental retardation.
    Palka-Bayard-de-Volo C; De Marco S; Chiavaroli V; Alfonsi M; Calabrese G; Chiarelli F; Mohn A
    Gene; 2012 Aug; 504(1):107-10. PubMed ID: 22583828
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Coexistence of inverted Y, chromosome 15p+ and abnormal phenotype.
    Acar H; Cora T; Erkul I
    Genet Couns; 1999; 10(2):163-70. PubMed ID: 10422010
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Structural chromosomal abnormalities in patients with mental retardation and/or multiple congenital anomalies: a new series of 24 patients.
    Tos T; Karaman A; Aksoy A; Tukun A
    Genet Couns; 2012; 23(2):289-96. PubMed ID: 22876589
    [TBL] [Abstract][Full Text] [Related]  

  • 18. [Molecular cytogenetic studies of 25 males with azoospermia].
    Ge YS; Zhou YL; Wu HN
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2008 Apr; 25(2):190-4. PubMed ID: 18393244
    [TBL] [Abstract][Full Text] [Related]  

  • 19. [Structural abnormalities of the Y chromosome. Observations in ten cases].
    Mattei JF; Mattei MG; Lucas C; Giraud F
    J Genet Hum; 1979 Mar; 27(1):53-66. PubMed ID: 479854
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Characterisation of a satellited non-fluorescent Y chromosome (Y[nfqs]) by FISH.
    Verma RS; Gogineni SK; Kleyman SM; Conte RA
    J Med Genet; 1997 Oct; 34(10):817-8. PubMed ID: 9350813
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 6.