BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

70 related articles for article (PubMed ID: 15905641)

  • 1. Inherited pericentric inversion (X)(p11.4q11.2) associated with delayed puberty and obesity in two brothers.
    Talaban R; Sellick GS; Spendlove HE; Howell R; King C; Reckless J; Newbury-Ecob R; Houlston RS
    Cytogenet Genome Res; 2005; 109(4):480-4. PubMed ID: 15905641
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Molecular cytogenetic characterization of a familial pericentric inversion 3 associated with short stature.
    Dutta UR; Hansmann I; Schlote D
    Eur J Med Genet; 2015 Mar; 58(3):154-9. PubMed ID: 25595572
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Breakpoint analysis of the pericentric inversion between chimpanzee chromosome 10 and the homologous chromosome 12 in humans.
    Kehrer-Sawatzki H; Sandig CA; Goidts V; Hameister H
    Cytogenet Genome Res; 2005; 108(1-3):91-7. PubMed ID: 15545720
    [TBL] [Abstract][Full Text] [Related]  

  • 4. A pericentric inversion of chromosome X disrupting
    Xin Y; Zhou J; Ding Q; Chen C; Wu X; Wang X; Wang H; Jiang X
    J Clin Pathol; 2017 Aug; 70(8):656-661. PubMed ID: 28073995
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Breakpoint analysis of the pericentric inversion distinguishing human chromosome 4 from the homologous chromosome in the chimpanzee (Pan troglodytes).
    Kehrer-Sawatzki H; Sandig C; Chuzhanova N; Goidts V; Szamalek JM; Tänzer S; Müller S; Platzer M; Cooper DN; Hameister H
    Hum Mutat; 2005 Jan; 25(1):45-55. PubMed ID: 15580561
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Molecular characterization of the pericentric inversion of chimpanzee chromosome 11 homologous to human chromosome 9.
    Kehrer-Sawatzki H; Szamalek JM; Tänzer S; Platzer M; Hameister H
    Genomics; 2005 May; 85(5):542-50. PubMed ID: 15820305
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Cloning of the breakpoints of a de novo inversion of chromosome 8, inv (8)(p11.2q23.1) in a patient with Ambras syndrome.
    Tadin-Strapps M; Warburton D; Baumeister FA; Fischer SG; Yonan J; Gilliam TC; Christiano AM
    Cytogenet Genome Res; 2004; 107(1-2):68-76. PubMed ID: 15305058
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Positional cloning strategies for idiopathic scoliosis.
    Bashiardes S; Veile R; Wise CA; Szappanos L; Lovett M
    Stud Health Technol Inform; 2002; 91():86-9. PubMed ID: 15457700
    [TBL] [Abstract][Full Text] [Related]  

  • 9. 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]  

  • 10. Pericentric inversion inv(7)(p11q21.1): report on two cases and genotype-phenotype correlations.
    Vorsanova SG; Iourov IY; Demidova IA; Kolotii AD; Soloviev IV; Yurov YB
    Tsitol Genet; 2006; 40(3):45-8. PubMed ID: 16933852
    [TBL] [Abstract][Full Text] [Related]  

  • 11. The evolutionary history of human chromosome 7.
    Müller S; Finelli P; Neusser M; Wienberg J
    Genomics; 2004 Sep; 84(3):458-67. PubMed ID: 15498453
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Beckwith-Wiedemann syndrome due to 11p15.5 paternal duplication associated with Klinefelter syndrome and a "de novo" pericentric inversion of chromosome Y.
    Delicado A; Lapunzina P; Palomares M; Molina MA; Galán E; López Pajares I
    Eur J Med Genet; 2005; 48(2):159-66. PubMed ID: 16053907
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Meiotic segregation analysis in spermatozoa of pericentric inversion carriers using fluorescence in-situ hybridization.
    Morel F; Laudier B; Guérif F; Couet ML; Royère D; Roux C; Bresson JL; Amice V; De Braekeleer M; Douet-Guilbert N
    Hum Reprod; 2007 Jan; 22(1):136-41. PubMed ID: 16917123
    [TBL] [Abstract][Full Text] [Related]  

  • 14. X-linked ichthyosis with hypogonadism: not always Kallmann's syndrome.
    Quinton R; Schofield JK; Duke VM; Bouloux PM; Buchanan CR; Leigh IM; Wood DF
    Clin Exp Dermatol; 1997 Jul; 22(4):201-4. PubMed ID: 9499614
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Inversion (X)(p11.4q22) associated with Norrie disease in a four generation family.
    Pettenati MJ; Rao PN; Weaver RG; Thomas IT; McMahan MR
    Am J Med Genet; 1993 Mar; 45(5):577-80. PubMed ID: 8456827
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Analysis of balanced rearrangements of chromosome 6 in acute leukemia: clustered breakpoints in q22-q23 and possible involvement of c-MYB in a new recurrent translocation, t(6;7)(q23;q32 through 36).
    Sinclair P; Harrison CJ; Jarosová M; Foroni L
    Haematologica; 2005 May; 90(5):602-11. PubMed ID: 15921375
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Genetic counselling in carriers of reciprocal chromosomal translocations involving short arm of chromosome X.
    Panasiuk B; Usinskiené R; Kostyk E; Rybałko A; Stasiewicz-Jarocka B; Krzykwa B; Pieńkowska-Grela B; Kucinskas V; Michalova K; Midro AT
    Ann Genet; 2004; 47(1):11-28. PubMed ID: 15050871
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Rare interstitial deletion (2)(p11.2p13) in a child with pericentric inversion (2)(p11.2q13) of paternal origin.
    Lacbawan FL; White BJ; Anguiano A; Rigdon DT; Ball KD; Bromage GB; Yang X; DiFazio MP; Levin SW
    Am J Med Genet; 1999 Nov; 87(2):139-42. PubMed ID: 10533028
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Monosomy 19pter and trisomy 19q13-qter in two siblings arising from a maternal pericentric inversion: clinical data and molecular characterization.
    Schluth-Bolard C; Till M; Rafat A; Labalme A; Le Lorc'h M; Banquart E; Angei C; Cordier MP; Romana SP; Edery P; Sanlaville D
    Eur J Med Genet; 2008; 51(6):622-30. PubMed ID: 18674648
    [TBL] [Abstract][Full Text] [Related]  

  • 20. [Cytogenetic study of a case of Fanconi's syndrome with a familial pericentric inversion].
    Crippa L; Ferrier S
    J Genet Hum; 1975 Mar; 23(1):7-16. PubMed ID: 1165481
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 4.