BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

100 related articles for article (PubMed ID: 10677904)

  • 1. [The Schmid-Fraccaro syndrome].
    Kollárová A; Misovicová N; Mális V
    Cesk Slov Oftalmol; 1999 Nov; 55(6):362-6. PubMed ID: 10677904
    [TBL] [Abstract][Full Text] [Related]  

  • 2. [Atypical cat eye syndrome. Fluorescence in situ hybridization of metaphase chromosomes].
    Bartsch O; Aksu F; Fenner A; Schwinger E
    Monatsschr Kinderheilkd; 1992 Aug; 140(8):460-3. PubMed ID: 1359403
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Schmid-Fraccaro syndrome: severe neurologic features.
    Romagna ES; Appel da Silva MC; Ballardin PA
    Pediatr Neurol; 2010 Feb; 42(2):151-3. PubMed ID: 20117756
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Cytogenetic characterization of cat eye syndrome marker chromosome.
    Wenger SL; Surti U; Nwokoro NA; Steele MW
    Ann Genet; 1994; 37(1):33-6. PubMed ID: 8010712
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Phenotypic variability of the cat eye syndrome. Case report and review of the literature.
    Rosias PR; Sijstermans JM; Theunissen PM; Pulles-Heintzberger CF; De Die-Smulders CE; Engelen JJ; Van Der Meer SB
    Genet Couns; 2001; 12(3):273-82. PubMed ID: 11693792
    [TBL] [Abstract][Full Text] [Related]  

  • 6. FISH of supernumerary marker chromosomes (SMCs) identifies six diagnostically relevant intervals on chromosome 22q and a novel type of bisatellited SMC(22).
    Bartsch O; Rasi S; Hoffmann K; Blin N
    Eur J Hum Genet; 2005 May; 13(5):592-8. PubMed ID: 15756300
    [TBL] [Abstract][Full Text] [Related]  

  • 7. FISH approach to determine cat eye syndrome chromosome breakpoints of a patient with cat eye syndrome type II.
    Gentile M; De Sanctis S; Cariola F; Spezzi T; Di Carlo A; Tontoli F; Lista F; Buonadonna AL
    Eur J Med Genet; 2005; 48(1):33-9. PubMed ID: 15953404
    [TBL] [Abstract][Full Text] [Related]  

  • 8. A new case of a severe clinical phenotype of the cat-eye syndrome.
    Denavit TM; Malan V; Grillon C; Sanlaville D; Ardalan A; Jacquemont ML; Burglen L; Taillemite JL; Portnoi MF
    Genet Couns; 2004; 15(4):443-8. PubMed ID: 15658620
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Delineation of a supernumerary marker chromosome utilizing a multimodal approach of G-banding, fluorescent in situ hybridization, confirmatory P1 artificial chromosome fluorescent in situ hybridization, and high-resolution comparative genomic hybridization.
    Mark HF; Wyandt H; Huang XL; Milunsky JM
    Clin Genet; 2005 Aug; 68(2):146-51. PubMed ID: 15996211
    [TBL] [Abstract][Full Text] [Related]  

  • 10. [Coloboma of the iris and anal atresia. Cat eye syndrome. Schmid-Fraccaro's syndrome].
    Vestermark S
    Ugeskr Laeger; 1975 Oct; 137(43):2525. PubMed ID: 1189049
    [No Abstract]   [Full Text] [Related]  

  • 11. Duane's syndrome and 22 marker chromosome: a possible cat-eye syndrome.
    Gómez-Lado C; Eirís J; Martínez-Yriarte JM; Blanco O; Castro-Gago M
    Acta Paediatr; 2006 Nov; 95(11):1510-1. PubMed ID: 17062489
    [No Abstract]   [Full Text] [Related]  

  • 12. Identification of autosomal supernumerary chromosome markers (SMCs) by fluorescent in situ hybridization (FISH).
    Kolialexi A; Kitsiou S; Fryssira H; Sofocleous C; Kouvidi E; Tsangaris GT; Salavoura K; Mavrou A
    In Vivo; 2006; 20(4):473-8. PubMed ID: 16900777
    [TBL] [Abstract][Full Text] [Related]  

  • 13. A hereditary bisatellite-dicentric supernumerary chromosome in a case of cat-eye syndrome.
    Lüleci G; Bağci G; Kivran M; Lüleci E; Bektaş S; Başaran S
    Hereditas; 1989; 111(1):7-10. PubMed ID: 2793513
    [TBL] [Abstract][Full Text] [Related]  

  • 14. A dysmorphic newborn infant with a complex rearrangement involving chromosomes 2, 4, and 6 detected by fluorescence in situ hybridization (FISH).
    Hoffman DJ; Punnett HH; Pyeritz RE
    Am J Perinatol; 2004 Feb; 21(2):69-71. PubMed ID: 15017469
    [TBL] [Abstract][Full Text] [Related]  

  • 15. 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]  

  • 16. Small supernumerary marker chromosome derived from proximal p-arm of chromosome 2: identification by fluorescent in situ hybridization.
    Lasan Trcić R; Hitrec V; Letica L; Cuk M; Begović D
    Croat Med J; 2003 Aug; 44(4):477-9. PubMed ID: 12950153
    [TBL] [Abstract][Full Text] [Related]  

  • 17. [An unusual syndrome: colobomatous disorder of the eyeball, anal atresia, multiple congenital anomalies and presence of an extra chromosome].
    Thomas C; Cordier J; Gilgenkrantz S; Reny A; Raspiller A
    Ann Ocul (Paris); 1969 Oct; 202(10):1021-31. PubMed ID: 4983376
    [No Abstract]   [Full Text] [Related]  

  • 18. The Montgomery lecture, 1977. Curious colobomata.
    Mullaney J
    Trans Ophthalmol Soc U K (1962); 1977 Sep; 97(4):517-22. PubMed ID: 103250
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Typical and partial cat eye syndrome: identification of the marker chromosome by FISH.
    Liehr T; Pfeiffer RA; Trautmann U
    Clin Genet; 1992 Aug; 42(2):91-6. PubMed ID: 1424237
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Aniridia, congenital glaucoma, and hydrocephalus in a male infant with ring chromosome 6.
    Levin H; Ritch R; Barathur R; Dunn MW; Teekhasaenee C; Margolis S
    Am J Med Genet; 1986 Oct; 25(2):281-7. PubMed ID: 3777023
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 5.