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 *

122 related articles for article (PubMed ID: 2887318)

  • 1. Familial transmission of a ring chromosome 21.
    Hertz JM
    Clin Genet; 1987 Jul; 32(1):35-9. PubMed ID: 2887318
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Ring chromosome 21 transmitted from mother to daughter: its stability in a lymphoblastoid cell line.
    Ikeuchi T; Yamamoto K; Qiao F; Hayakawa K; Migita T; Nishikawa Y
    Ann Genet; 1990; 33(1):32-5. PubMed ID: 2369070
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Transmission of a ring chromosome 18 from a mother with 46,XX/47,XX, + r(18) mosaicism to her daughter, resulting in a 46,XX,r(18) karyotype.
    Jenderny J; Caliebe A; Beyer C; Grote W
    J Med Genet; 1993 Nov; 30(11):964-5. PubMed ID: 8301656
    [TBL] [Abstract][Full Text] [Related]  

  • 4. [A familial case of 17 r ring-shaped chromosome of group E with transmission from father to son].
    Burden M; Lupaşcu E; Mărgineanu L
    Rev Med Chir Soc Med Nat Iasi; 1973; 77(2):353-7. PubMed ID: 4146973
    [No Abstract]   [Full Text] [Related]  

  • 5. [Prenatal diagnosis of 3 cases of ring G chromosomes: one 21 and two 22, one of which was de novo].
    Crusi A; Engel E
    Ann Genet; 1986; 29(4):253-60. PubMed ID: 3495227
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Familial ring (19) chromosome mosaicism: case report and review.
    Flejter WL; Finlinson D; Root S; Nguyen W; Brothman AR; Viskochil D
    Am J Med Genet; 1996 Dec; 66(3):276-80. PubMed ID: 8985487
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Apparent monosomy 21 owing to a ring 21 chromosome: parental origin revealed by DNA analysis.
    Dalgleish R; Duckett DP; Woodhouse M; Shannon RS; Young ID
    J Med Genet; 1988 Dec; 25(12):851-4. PubMed ID: 3236369
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Investigation of three patients with the "ring syndrome", including familial transmission of ring 5, and estimation of reproductive risks.
    MacDermot KD; Jack E; Cooke A; Turleau C; Lindenbaum RH; Pearson J; Patel C; Barnes PM; Portch J; Crawfurd MD
    Hum Genet; 1990 Oct; 85(5):516-20. PubMed ID: 2227937
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Identification of marker chromosomes in thirteen patients using FISH probing.
    Daniel A; Malafiej P; Preece K; Chia N; Nelson J; Smith M
    Am J Med Genet; 1994 Oct; 53(1):8-18. PubMed ID: 7802042
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Interstitial deletion and ring chromosome derived from 16q.
    Krauss CM; Caldwell D; Atkins L
    J Med Genet; 1987 May; 24(5):308-12. PubMed ID: 3585948
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Ring chromosome 18 in a mother and son.
    Donlan MA; Dolan CR
    Am J Med Genet; 1986 May; 24(1):171-4. PubMed ID: 3706404
    [TBL] [Abstract][Full Text] [Related]  

  • 12. [A case of an XX man with presence of H-Y antigen in his mother].
    Caporal R; Petit P; Wauthier JL; Segrestaa JM
    Ann Med Interne (Paris); 1985; 136(8):646-9. PubMed ID: 2870673
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Complex chromosomal rearrangement and multiple spontaneous abortions.
    Gorski JL; Emanuel BS; Zackai EH; Mennuti M
    Hum Genet; 1986 Nov; 74(3):326. PubMed ID: 3781562
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Application of fluorescence in situ hybridization to the identification of different marker chromosomes.
    Verschraegen-Spae MR; Quack B; Rousseaux S; Pison H; Messiaen L; De Paepe A; Lespinasse J
    Ann Genet; 1998; 41(1):5-10. PubMed ID: 9599644
    [TBL] [Abstract][Full Text] [Related]  

  • 15. [Cytogenetic analysis and phenotype location analysis on the karyotype of a ring chromosome 21 syndrome].
    Zhu XY; Zhao R; Ye ZC; Peng YG; Tan YQ
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2005 Dec; 22(6):682-3. PubMed ID: 16331572
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Identification and characterisation of a small marker chromosome using non-isotopic in situ hybridisation with X and Y specific probes.
    Crolla JA; Smith M; Docherty Z
    J Med Genet; 1989 Mar; 26(3):192-4. PubMed ID: 2709396
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Transmission of ring chromosome 18 46,XX/46,XX,r(18) mosaicism in a mother and ring chromosome 18 syndrome in her son.
    Fryns JP; Kleczkowska A; Smeets E; Van Den Berghe H
    Ann Genet; 1992; 35(2):121-3. PubMed ID: 1524410
    [TBL] [Abstract][Full Text] [Related]  

  • 18. An 11-year-old boy with mosaic ring chromosome 6 and dilated aortic root.
    Ivanovich JL; Watson MS; Whelan AJ
    Am J Med Genet; 2001 Jan; 98(2):182-4. PubMed ID: 11223855
    [TBL] [Abstract][Full Text] [Related]  

  • 19. [Transmission of an 18 ring chromosome in two generations in subjects of normal phenotype].
    Faugeras C; Barthe D
    J Genet Hum; 1986 Aug; 34(3-4):313-20. PubMed ID: 3760834
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Chromosomal anomalies in cryptorchidism and hypospadias.
    Yamaguchi T; Kitada S; Osada Y
    Urol Int; 1991; 47(2):60-3. PubMed ID: 1686509
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 7.