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 *

110 related articles for article (PubMed ID: 16293919)

  • 1. Cat-eye syndrome with isolated idiopathic hypogonadotropic hypogonadism.
    Matsumoto R; Shimizu C; Nagai S; Taniguchi S; Umetsu M; Kimura Y; Atsumi T; Yoshioka N; Kubo M; Koike T
    Intern Med; 2005 Oct; 44(10):1069-73. PubMed ID: 16293919
    [TBL] [Abstract][Full Text] [Related]  

  • 2. [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]  

  • 3. 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]  

  • 4. Cat eye syndrome with hypogonadotropic hypogonadism.
    Masukawa H; Ozaki T; Nogimori T
    Intern Med; 1998 Oct; 37(10):853-6. PubMed ID: 9840707
    [TBL] [Abstract][Full Text] [Related]  

  • 5. 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]  

  • 6. 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]  

  • 7. 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]  

  • 8. 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]  

  • 9. 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]  

  • 10. [Associated brachial cleft anomalies in the cat eye syndrome].
    Avior G; Derowe A; Fliss DM; Leicear-Trejo L; Braverman I
    Harefuah; 2007 Feb; 146(2):99-101, 166-7. PubMed ID: 17352276
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Intrachromosomal duplications of 22q11 are not a common cause of isolated coloboma and coloboma with other limited features of cat eye syndrome.
    Raca G; Schimmenti L; Martin CL
    Am J Med Genet A; 2008 Feb; 146A(3):401-4. PubMed ID: 18203172
    [No Abstract]   [Full Text] [Related]  

  • 12. 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]  

  • 13. 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]  

  • 14. 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]  

  • 15. [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]  

  • 16. Congenital hypopituitarism and multiple midline defects in a newborn with non-familial Cat Eye syndrome.
    Serra G; Giambrone C; Antona V; Cardella F; Carta M; Cimador M; Corsello G; Giuffrè M; Insinga V; Maggio MC; Pensabene M; Schierz IAM; Piro E
    Ital J Pediatr; 2022 Sep; 48(1):170. PubMed ID: 36076277
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Schmid-Fraccaro syndrome ("cat's eye" syndrome).
    Petersen RA
    Arch Ophthalmol; 1973 Oct; 90(4):287-91. PubMed ID: 4746642
    [No Abstract]   [Full Text] [Related]  

  • 18. [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]  

  • 19. [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]  

  • 20. [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]  

    [Next]    [New Search]
    of 6.