BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

141 related articles for article (PubMed ID: 1165480)

  • 1. Trisomy 22.
    Zellweger H; Ionasescu V; Simpson J
    J Genet Hum; 1975 Mar; 23(1):65-75. PubMed ID: 1165480
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Cat-eye syndrome with unusual marker chromosome probably not chromosome 22.
    Rosenfeld W; Verma RS; Jhaveri RC
    Am J Med Genet; 1984 May; 18(1):19-24. PubMed ID: 6588751
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Parental origin of the extra chromosome in the cat eye syndrome: evidence from heteromorphism and in situ hybridization analysis.
    Magenis RE; Sheehy RR; Brown MG; McDermid HE; White BN; Zonana J; Weleber R
    Am J Med Genet; 1988 Jan; 29(1):9-19. PubMed ID: 3344779
    [TBL] [Abstract][Full Text] [Related]  

  • 4. The aetiology of the cat eye syndrome reconsidered.
    Guanti G
    J Med Genet; 1981 Apr; 18(2):108-18. PubMed ID: 7241528
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Identification of a cat eye syndrome using DNA sequence dosage analysis.
    Bulle F; Lespinasse J; Pawlak A; Vadot E; Sastre J; Noël B; Guellaen G
    Ann Genet; 1996; 39(3):139-43. PubMed ID: 8839885
    [TBL] [Abstract][Full Text] [Related]  

  • 6. [Partial trisomy of the short arm of chromosome 3. Case report and phenotype expression].
    Frankova YE; Holenova H; Braulke I
    Monatsschr Kinderheilkd; 1991 Dec; 139(12):841-3. PubMed ID: 1770961
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Inverted duplication of 22pter----q11.21 in cat-eye syndrome.
    Hoo JJ; Robertson A; Fowlow SB; Bowen P; Lin CC
    Am J Med Genet; 1986 Jul; 24(3):543-5. PubMed ID: 3728573
    [No Abstract]   [Full Text] [Related]  

  • 8. Trisomy iop. A report of two cases due to a familial translocation rcp (10;21) (pII;pII).
    Cantu JM; Salamanca F; Buentello L; Carnevale A; Armendares S
    Ann Genet; 1975 Mar; 18(1):5-11. PubMed ID: 1080038
    [TBL] [Abstract][Full Text] [Related]  

  • 9. [Extra mini-chromosome with symptoms of cat-eye syndrome].
    Méhes K; Bajnóczky K; Schmidt P
    Orv Hetil; 1985 Apr; 126(17):1037-9. PubMed ID: 3991187
    [No Abstract]   [Full Text] [Related]  

  • 10. Re-evaluation of the supernumerary chromosome in an individual with cat eye syndrome.
    Duncan AM; Rosenfeld W; Verma RS
    Am J Med Genet; 1987 May; 27(1):225-7. PubMed ID: 3474897
    [No Abstract]   [Full Text] [Related]  

  • 11. Phenotype-karyotype correlations in dup(18q): report of a case and review.
    Razavi-Encha F; Raoul O; Lescs MC; Danan C
    Am J Med Genet; 1985 Jul; 21(3):591-5. PubMed ID: 4025391
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Cleft palate and multiple anomalies in one of two siblings with partial 13 trisomy.
    Kaye CI; Booth CW; Meeker D; Nadler HL
    Cleft Palate J; 1977 Jul; 14(3):244-8. PubMed ID: 267527
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Silver staining of the supernumerary chromosome in the cat-eye syndrome.
    Petit P; Godart S; Fryns JP
    Ann Genet; 1980; 23(2):114-6. PubMed ID: 6156636
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Cat-eye syndrome: evaluation of the extra chromosome with banding techniques. Case report.
    De Chieri R; Malfatti C; Stanchi F; Albores JM
    J Genet Hum; 1974 Jun; 22(2):101-7. PubMed ID: 4213897
    [No Abstract]   [Full Text] [Related]  

  • 15. Partial trisomy 10p12.33 and partial monosomy 13q32.1: case report and a literature review.
    Puvabanditsin S; Garrow E; Lambert G; Botti C; Gowda S; Kathiravan S; Brooks SS
    Genet Couns; 2011; 22(3):263-72. PubMed ID: 22029167
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Case report. The cat-eye syndrome with unusual skeletal malformations.
    Balci S; Halicioglu C; Say B; Taysi K
    Acta Paediatr Scand; 1974 Jul; 63(4):623-6. PubMed ID: 4850902
    [No Abstract]   [Full Text] [Related]  

  • 17. E trisomy phenotype associated with small metacentric chromosome and a familial Y-22 translocation.
    Dumars KW; Fialko G; Larson E
    Birth Defects Orig Artic Ser; 1976; 12(5):97-104. PubMed ID: 953249
    [TBL] [Abstract][Full Text] [Related]  

  • 18. [Coloboma and anal atresia: phenotype of a chromosome aberration?].
    Pfeiffer RA; Heimann K; Heiming E; Schlack H; Maul H
    Klin Monbl Augenheilkd; 1971 Sep; 159(3):357-67. PubMed ID: 5003627
    [No Abstract]   [Full Text] [Related]  

  • 19. Trisomy 22 in a liveborn infant with multiple congenital anomalies.
    McPherson E; Stetka DG
    Am J Med Genet; 1990 May; 36(1):11-4. PubMed ID: 2333899
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Familial 10p trisomy resulting from a maternal pericentric inversion.
    Kozma C; Meck JM
    Am J Med Genet; 1994 Feb; 49(3):281-7. PubMed ID: 8209887
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 8.