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 *

256 related articles for article (PubMed ID: 7241528)

  • 21. 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]  

  • 22. Anal atresia, eye anomalies, and an additional small abnormal acrocentric chromosome (47,XX,mar+): report of a case.
    Weber FM; Dooley RR; Sparkes RS
    J Pediatr; 1970 Apr; 76(4):594-7. PubMed ID: 5420796
    [No Abstract]   [Full Text] [Related]  

  • 23. 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]  

  • 24. [Ocular findings in chromosome diseases].
    Cagianut B
    Ophthalmologica; 1968; 155(2):148-66. PubMed ID: 4965902
    [No Abstract]   [Full Text] [Related]  

  • 25. Partial trisomy of chromosome 22 resulting from a supernumerary marker chromosome 22 in a child with features of cat eye syndrome.
    Bélien V; Gérard-Blanluet M; Serero S; Le Dû N; Baumann C; Jacquemont ML; Dupont C; Krabchi K; Drunat S; Elbez A; Janaud JC; Benzacken B; Verloes A; Tabet AC; Aboura A
    Am J Med Genet A; 2008 Jul; 146A(14):1871-4. PubMed ID: 18553551
    [TBL] [Abstract][Full Text] [Related]  

  • 26. 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]  

  • 27. Pseudoisodicentric bisatellited extra marker chromosome (tetrasomy 22pter----q11, trisomy Yqh), derived from a maternal Y/22 translocation. Association between this tetrasomy and "cat eye" phenotypical features.
    Gabarrón J; Glover G; Jimenez A; Lamata E
    Clin Genet; 1985 Dec; 28(6):509-15. PubMed ID: 3865751
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Characterization of the supernumerary chromosome in cat eye syndrome.
    McDermid HE; Duncan AM; Brasch KR; Holden JJ; Magenis E; Sheehy R; Burn J; Kardon N; Noel B; Schinzel A
    Science; 1986 May; 232(4750):646-8. PubMed ID: 3961499
    [TBL] [Abstract][Full Text] [Related]  

  • 29. An inherited translocation t(4;15) (p16;q22) leading to two cases of partial trisomy 15.
    Cohen MM; Ornoy A; Rosenmann A; Kohn G
    Ann Genet; 1975 Jun; 18(2):99-103. PubMed ID: 1081372
    [TBL] [Abstract][Full Text] [Related]  

  • 30. 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]  

  • 31. 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]  

  • 32. Partial trisomy 8p (8p11.2-->pTER) and deletion of 13q (13q32-->qTER): case report.
    Yeşilyurt A; Dilli D; Oguz S; Dilmen U; Altug N; Candemir Z
    Genet Couns; 2011; 22(1):35-40. PubMed ID: 21614986
    [TBL] [Abstract][Full Text] [Related]  

  • 33. 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]  

  • 34. A case of partial trisomy 2p23-pter syndrome with trisomy 18p due to a de novo supernumerary marker chromosome.
    Lee JH; Cho HS; Lee ES; Jung BC
    Korean J Lab Med; 2010 Jun; 30(3):312-7. PubMed ID: 20603594
    [TBL] [Abstract][Full Text] [Related]  

  • 35. 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]  

  • 36. Trisomy 18 in a patient with CHARGE association.
    Lee WT; Hou JW; Yau KI; Wang TR
    J Formos Med Assoc; 1995; 94(1-2):60-2. PubMed ID: 7613237
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Trisomy 20p: case report and genetic review.
    Lurie IW; Rumyantseva NV; Zaletajev DV; Gurevich DB; Korotkova IA
    J Genet Hum; 1985 Jan; 33(1):67-75. PubMed ID: 3981145
    [TBL] [Abstract][Full Text] [Related]  

  • 38. 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]  

  • 39. 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]  

  • 40. The problem of trisomy 22. A case report and a discussion of the variant forms.
    Zellweger H; Ionasescu V; Simpson J; Burmeister L
    Clin Pediatr (Phila); 1976 Jul; 15(7):601-6, 617-8. PubMed ID: 819199
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 13.