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 *

158 related articles for article (PubMed ID: 336892)

  • 1. Trisomy 22 with 'cat eye' anomaly.
    Cervenka J; Hansen CA; Franciosi RA; Gorlin RJ
    J Med Genet; 1977 Aug; 14(4):288-90. PubMed ID: 336892
    [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. Cat eye syndrome. Partial trisomy 22 due to translocation in the mother.
    Bofinger MK; Soukup SW
    Am J Dis Child; 1977 Aug; 131(8):893-97. PubMed ID: 888806
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Confirmation of trisomy 22 by trypsin-giemsa staining.
    Begleiter ML; Kulkarni P; Harris DJ
    J Med Genet; 1976 Dec; 13(6):517-20. PubMed ID: 138743
    [TBL] [Abstract][Full Text] [Related]  

  • 6. 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]  

  • 7. 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]  

  • 8. The "cat eye syndrome": dicentric small marker chromosome probably derived from a no.22 (tetrasomy 22pter to q11) associated with a characteristic phenotype. Report of 11 patients and delineation of the clinical picture.
    Schinzel A; Schmid W; Fraccaro M; Tiepolo L; Zuffardi O; Opitz JM; Lindsten J; Zetterqvist P; Enell H; Baccichetti C; Tenconi R; Pagon RA
    Hum Genet; 1981; 57(2):148-58. PubMed ID: 6785205
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Cytogenetic investigation of cat-eye syndrome.
    Walknowska J; Peakman D; Weleber RG
    Am J Ophthalmol; 1977 Oct; 84(4):477-86. PubMed ID: 410302
    [TBL] [Abstract][Full Text] [Related]  

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

  • 11. Trisomy 22. Two new cases and delineation of the phenotype.
    Penchaszadeh VB; Coco R
    J Med Genet; 1975 Jun; 12(2):193-9. PubMed ID: 49427
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Cebocephaly in an infant with trisomy 18.
    Hunter AG; Ray M; Langston C
    J Med Genet; 1977 Aug; 14(4):291-2. PubMed ID: 411936
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Patau's syndrome and 13q21q translocation.
    Pérez-Castillo A; Abrisqueta JA
    Hum Genet; 1978 Jun; 42(3):327-31. PubMed ID: 669714
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Trisomy 11q(q21 leads to qter).
    Bader PI; Jansch M; Hoffman D; Palmer CG; Gerber H; Taylor G
    Birth Defects Orig Artic Ser; 1978; 14(6C):383-92. PubMed ID: 728594
    [No Abstract]   [Full Text] [Related]  

  • 15. Ocular movement disturbances in a family with trisomy 22 syndrome.
    Sebestyén J; Méhes K
    Ophthalmologica; 1973; 166(5):360-71. PubMed ID: 4730727
    [No Abstract]   [Full Text] [Related]  

  • 16. Brief Clinical Report: coloboma hypospadias.
    Halal F; Farsky K
    Am J Med Genet; 1981; 8(1):53-8. PubMed ID: 7246606
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Trisomy 18 syndrome with an unusual karyotype: possible double isochromosome.
    Larson LM; Wasdahl WA; Saumur JH; Coleman ML; Jalal SM
    J Med Genet; 1978 Feb; 15(1):73-6. PubMed ID: 633320
    [TBL] [Abstract][Full Text] [Related]  

  • 18. [Minor ocular manifestations in a case of D trisomy by 13-14 translocation. Coloboma of the iris, congenital retinal fold, without microphthalmia or choroid coloboma].
    Seringe P; Dhermy P; Loewe-Lyon S; Despres P; Aron JJ
    Arch Ophtalmol Rev Gen Ophtalmol; 1971; 31(6):497-516. PubMed ID: 4255267
    [No Abstract]   [Full Text] [Related]  

  • 19. 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]  

  • 20. 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]  

    [Next]    [New Search]
    of 8.