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 *

108 related articles for article (PubMed ID: 2641076)

  • 21. Familial pericentric inversion of chromosome 8.
    Sujansky E; Smith AC; Peakman DC; McConnell TS; Baca P; Robinson A
    Am J Med Genet; 1981; 10(3):229-35. PubMed ID: 6171164
    [TBL] [Abstract][Full Text] [Related]  

  • 22. 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]  

  • 23. De novo 13q paracentric inversion in a boy with cleft palate and mental retardation.
    Riccardi VM; Holmquist GP
    Hum Genet; 1979 Nov; 52(2):211-5. PubMed ID: 511176
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Interstitial 3p deletion in a child due to paternal paracentric inserted inversion.
    Wyandt HE; Kasprzak R; Ennis J; Willson K; Koch V; Schnatterly P; Wilson W; Kelly TE
    Am J Hum Genet; 1980 Sep; 32(5):731-5. PubMed ID: 7424912
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Updating advances in cytogenetics. Applications of the new chromosome banding methods.
    Breg WR
    Birth Defects Orig Artic Ser; 1974; 10(8):7-18. PubMed ID: 4142402
    [No Abstract]   [Full Text] [Related]  

  • 26. Ectopic posterior pituitary tissue and paracentric inversion of the short arm of chromosome 1 in twins.
    Siegel SF; Ahdab-Barmada M; Arslanian S; Foley TP
    Eur J Endocrinol; 1995 Jul; 133(1):87-92. PubMed ID: 7627343
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Sperm chromosome analysis in two cases of paracentric inversion.
    Vialard F; Delanete A; Clement P; Simon-Bouy B; Aubriot FX; Selva J
    Fertil Steril; 2007 Feb; 87(2):418.e1-5. PubMed ID: 17126336
    [TBL] [Abstract][Full Text] [Related]  

  • 28. A familial paracentric inv(1)(q42q44) resulting in a child with a del(1)(q42) karyotype.
    Speevak M; Hunter AG; Hughes H; Cox DM
    Ann Genet; 1985; 28(3):177-80. PubMed ID: 3879153
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Short rib-polydactyly syndrome and pericentric inversion of chromosome 4.
    Urioste M; Martínez-Frías ML; Bermejo E; Jiménez N; Romero D; Nieto C; Villa A
    Am J Med Genet; 1994 Jan; 49(1):94-7. PubMed ID: 7909650
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Stable dicentric duplication-deficiency chromosome 14 resulting from crossing-over within a maternal paracentric inversion.
    Lefort G; Blanchet P; Belgrade N; Rivier F; Chaze AM; Sarda P; Demaille J; Pellestor F
    Am J Med Genet; 2002 Dec; 113(4):333-8. PubMed ID: 12457404
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Human chromosome analysis: methodology and applications.
    Larson L
    Am J Med Technol; 1983 Oct; 49(10):687-98. PubMed ID: 6228140
    [TBL] [Abstract][Full Text] [Related]  

  • 32. A MELAS phenotype and a paternal inherited inversion of chromosome 10 in a female patient.
    Lorda-Sanchez I; Garcia-Ruiz PJ; Rodriguez de Alba M; Montoya J; Playan A; Sarasa JL; Trujillo MJ; Sanz R; Ramos C; Ayuso C
    Genet Couns; 2000; 11(3):261-5. PubMed ID: 11043434
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Characterization of complex chromosomal abnormalities in uveal melanoma by fluorescence in situ hybridization, spectral karyotyping, and comparative genomic hybridization.
    Naus NC; van Drunen E; de Klein A; Luyten GP; Paridaens DA; Alers JC; Ksander BR; Beverloo HB; Slater RM
    Genes Chromosomes Cancer; 2001 Mar; 30(3):267-73. PubMed ID: 11170284
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Vertical transmission of the Ohdo blepharophimosis syndrome.
    Mhanni AA; Dawson AJ; Chudley AE
    Am J Med Genet; 1998 May; 77(2):144-8. PubMed ID: 9605288
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Tetrasomy 18p: a distinctive syndrome.
    Rivera H; Möller M; Hernández A; Enríquez-Guerra MA; Arreola R; Cantú JM
    Ann Genet; 1984; 27(3):187-9. PubMed ID: 6334486
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Prenatal detection of de novo paracentric inversion 46, XX inv (14) (q22q32.1) in a normal child: report and review of the literature.
    Hales HA; Peterson CM; Carey J; Hecht BK; Hecht F
    Am J Med Genet; 1993 Nov; 47(6):848-51. PubMed ID: 8279482
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Paracentric inversions do not normally generate monocentric recombinant chromosomes.
    Sutherland GR; Callen DF; Gardner RJ
    Am J Med Genet; 1995 Nov; 59(3):390-2. PubMed ID: 8599369
    [No Abstract]   [Full Text] [Related]  

  • 38. [Trisomy 5p: a report of 2 cases].
    Alvarez-Coca J; García-Alix A; Delicado A; González M; Escribá R; López Pajares I; Morena V; Peralta A
    An Esp Pediatr; 1985 Mar; 22(4):288-92. PubMed ID: 4003955
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Protelomeric sequences are deleted in cases of short arm inverted duplication of chromosome 8.
    Barber JC; James RS; Patch C; Temple IK
    Am J Med Genet; 1994 Apr; 50(3):296-9. PubMed ID: 8042676
    [TBL] [Abstract][Full Text] [Related]  

  • 40. [Chromosome anomalies in human azoospermia].
    Sozanskiĭ OA; Guleniuk NL; Akopian GR; Zabrodskiĭ BT
    Genetika; 1988 Jul; 24(7):1299-303. PubMed ID: 3181753
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 6.