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 *

138 related articles for article (PubMed ID: 3970068)

  • 1. Tandem duplication of proximal 22q: a cause of cat-eye syndrome.
    Reiss JA; Weleber RG; Brown MG; Bangs CD; Lovrien EW; Magenis RE
    Am J Med Genet; 1985 Jan; 20(1):165-71. PubMed ID: 3970068
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Interstitial duplication of proximal 22q: phenotypic overlap with cat eye syndrome.
    Knoll JH; Asamoah A; Pletcher BA; Wagstaff J
    Am J Med Genet; 1995 Jan; 55(2):221-4. PubMed ID: 7717422
    [TBL] [Abstract][Full Text] [Related]  

  • 3. 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]  

  • 4. 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]  

  • 5. 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]  

  • 6. 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]  

  • 7. 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]  

  • 8. 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]  

  • 9. [Cat eye syndrome with pituitary dwarfism and normal mental development].
    Pierson M; Gilgenkrantz S; Saborio M
    Arch Fr Pediatr; 1975 Nov; 32(9):835-48. PubMed ID: 1217955
    [TBL] [Abstract][Full Text] [Related]  

  • 10. De novo tandem duplication of the middle segment of the long arm of chromosome 14.
    Ito M; Mutoh K; Okuno T; Mikawa H; Edagawa J; Abe T
    Ann Genet; 1983; 26(2):116-9. PubMed ID: 6604486
    [TBL] [Abstract][Full Text] [Related]  

  • 11. [Complex cyanotic heart defect in a newborn infant with cat eye syndrome].
    Paul T; Reimer A; Wilken M; Miller K; Kallfelz HC
    Monatsschr Kinderheilkd; 1991 Apr; 139(4):228-30. PubMed ID: 2072964
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Partial trisomy due to a de novo duplication 22q11.1-22q13.1: a cat-eye syndrome variant with brain anomalies.
    Karcaaltincaba D; Ceylaner S; Ceylaner G; Dalkilic S; Karli-Oguz K; Kandemir O
    Genet Couns; 2010; 21(1):19-24. PubMed ID: 20420025
    [TBL] [Abstract][Full Text] [Related]  

  • 13. [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]  

  • 14. De novo tandem duplication of chromosome segment 22q11-q12: clinical, cytogenetic, and molecular characterization.
    Lindsay EA; Shaffer LG; Carrozzo R; Greenberg F; Baldini A
    Am J Med Genet; 1995 Apr; 56(3):296-9. PubMed ID: 7778594
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Cat-eye syndrome with different marker chromosomes in a mother and daughter.
    Ing PS; Lubinsky MS; Smith SD; Golden E; Sanger WG; Duncan AM
    Am J Med Genet; 1987 Mar; 26(3):621-8. PubMed ID: 3105314
    [TBL] [Abstract][Full Text] [Related]  

  • 16. [Morphologic abnormality due to duplication of chromosome 17 (46,XY,17q+) in a newborn infant].
    Fouquette B; Rosenfeld R; Cadotte M
    Union Med Can; 1974 Aug; 103(8):1404-8. PubMed ID: 4849205
    [No Abstract]   [Full Text] [Related]  

  • 17. [Cat-eye syndrome].
    Neuhäuser G
    Hippokrates; 1973 Jun; 44(2):199-200. PubMed ID: 4754294
    [No Abstract]   [Full Text] [Related]  

  • 18. The 22q distal trisomy syndrome in a recombinant child.
    Rivera H; Garcia-Esquivel L; Romo MG; Perez-Garcia G; Martinez y Martinez R
    Ann Genet; 1988; 31(1):47-9. PubMed ID: 3258493
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Phenotypic variability of Cat-Eye syndrome.
    Berends MJ; Tan-Sindhunata G; Leegte B; van Essen AJ
    Genet Couns; 2001; 12(1):23-34. PubMed ID: 11332976
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Dynamic mosaicism involving an unstable supernumerary der(22) chromosome in cat eye syndrome.
    Urioste M; Visedo G; Sanchís A; Sentís C; Villa A; Ludeña P; Hortigüela JL; Martínez-Frías ML; Fernández-Piqueras J
    Am J Med Genet; 1994 Jan; 49(1):77-82. PubMed ID: 8172255
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 7.