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 *

104 related articles for article (PubMed ID: 8066046)

  • 1. Euchromatic heteromorphism or duplication without phenotypic effect?
    Barber JC
    Prenat Diagn; 1994 Apr; 14(4):323-4. PubMed ID: 8066046
    [No Abstract]   [Full Text] [Related]  

  • 2. A rare inherited euchromatic heteromorphism on chromosome 1.
    Zaslav AL; Blumenthal D; Fox JE; Thomson KA; Segraves R; Weinstein ME
    Prenat Diagn; 1993 Jul; 13(7):569-73. PubMed ID: 8415421
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Euchromatic 9q + heteromorphism in a family.
    Jalal SM; Kukolich MK; Garcia M; Day DW
    Am J Med Genet; 1990 Sep; 37(1):155-6. PubMed ID: 2240035
    [No Abstract]   [Full Text] [Related]  

  • 4. Rare chromosome 20 variants encountered during prenatal diagnosis.
    Petersen MB
    Prenat Diagn; 1986; 6(5):363-7. PubMed ID: 3774765
    [TBL] [Abstract][Full Text] [Related]  

  • 5. [Heteromorphism of chromosome 1, 9 and 16 homologs in persons living in regions differing in the level of longevity].
    Kuznetsova SM; Zaritskaia MIu; Berdyshev GD
    Tsitol Genet; 1988; 22(4):27-32. PubMed ID: 2973673
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Euchromatic 16p+ heteromorphism: first report in North America.
    Jalal SM; Schneider NR; Kukolich MK; Wilson GN
    Am J Med Genet; 1990 Dec; 37(4):548-50. PubMed ID: 2260607
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Two extra euchromatic bands in the qh region of chromosome 9.
    Ozkinay F; Ercal D; Ozkinay C; Onay H; Bora E; Erler A
    Genet Couns; 2005; 16(1):45-8. PubMed ID: 15844778
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Chromosome imbalance, normal phenotype, and imprinting.
    Bortotto L; Piovan E; Furlan R; Rivera H; Zuffardi O
    J Med Genet; 1990 Sep; 27(9):582-7. PubMed ID: 2231652
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Extra euchromatic band in the qh region of chromosome 9.
    von Beust G; Bink K
    Fetal Diagn Ther; 1999; 14(1):35-7. PubMed ID: 10072648
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Prenatal detection of de novo inversion of chromosome 9 with duplicated heterochromatic region and postnatal follow-up.
    Kim JJ; Rhee HS; Chung YT; Park SY; Choi SK
    Exp Mol Med; 1999 Sep; 31(3):134-6. PubMed ID: 10551261
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Prenatal diagnosis of a large centromeric heteromorphism of chromosome 12: implications for genetic counseling.
    Chantot-Bastaraud S; Siffroi JP; Berkane N; Heim N; Herve F; Uzan S; Vendrely E
    Fetal Diagn Ther; 2003; 18(2):111-3. PubMed ID: 12576746
    [TBL] [Abstract][Full Text] [Related]  

  • 12. [Cytogenetic study of a family with 15p+ chromosomal plymorphism].
    Manzanal Martínez AI; Robledo Batanero M; Ramos Corrales C; Ayuso García C; Sánchez Cascos A
    An Esp Pediatr; 1992 Apr; 36(4):269-71. PubMed ID: 1605408
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Euchromatic variant 16p+. Implications in prenatal diagnosis.
    López Pajares I; Villa O; Salido M; Mori MA; Gonzalez A; Lapunzina P; De Torres ML; Vallcorba I; Palomares M; Fernández L; Delicado A
    Prenat Diagn; 2006 Jun; 26(6):535-8. PubMed ID: 16634122
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Interstitial deletions without phenotypic effect: prenatal diagnosis of a new family and brief review.
    Barber JC; Mahl H; Portch J; Crawfurd MD
    Prenat Diagn; 1991 Jun; 11(6):411-6. PubMed ID: 1924182
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Familial occurrence of cancer and heteromorphism of the heterochromatic segment of chromosome 1.
    Köpf I; Islam MQ; Friberg LG; Levan G
    Hereditas; 1989; 110(1):79-83. PubMed ID: 2777631
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Duplication of 8p23.1: a cytogenetic anomaly with no established clinical significance.
    Barber JC; Joyce CA; Collinson MN; Nicholson JC; Willatt LR; Dyson HM; Bateman MS; Green AJ; Yates JR; Dennis NR
    J Med Genet; 1998 Jun; 35(6):491-6. PubMed ID: 9643291
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Minute chromosomal rearrangements detected prenatally by fluorescence in situ hybridization.
    Suzumori K; Tanemura M; Oya N; Suzumori N; Kim KC; Ohashi H; Fukushima Y
    Prenat Diagn; 1998 Jul; 18(7):725-30. PubMed ID: 9706655
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Prenatal diagnosis of a large heteromorphic region in a chromosome 5: implications for genetic counseling.
    Fineman RM; Issa B; Weinblatt V
    Am J Med Genet; 1989 Apr; 32(4):498-9. PubMed ID: 2773992
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Duplication of chromosome region 8p23.1-->p23.3: a benign variant?
    Engelen JJ; Moog U; Evers JL; Dassen H; Albrechts JC; Hamers AJ
    Am J Med Genet; 2000 Mar; 91(1):18-21. PubMed ID: 10751083
    [TBL] [Abstract][Full Text] [Related]  

  • 20. New chromosome aberration: duplication of a large part of chromosome 4q and partial deletion of chromosome 1q.
    Merlob P; Kohn G; Litwin A; Nissenkorn I; Katznelson MB; Reisner SH
    Am J Med Genet; 1989 Jan; 32(1):22-6. PubMed ID: 2705479
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 6.