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 *

136 related articles for article (PubMed ID: 1189049)

  • 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. The "cat eye" syndrome--report of a case with hypothyroidism.
    Ioan D; Dumitriu L; Fabriţius K; Simescu M; Maximilian C
    Endocrinologie; 1986; 24(2):129-31. PubMed ID: 3738402
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Maternal derivation of inv dup (22) and clinical variation in cat-eye syndrome.
    Tupler R; Hoeller A; Pezzolo A; Maraschio P
    Ann Genet; 1994; 37(3):153-5. PubMed ID: 7847799
    [TBL] [Abstract][Full Text] [Related]  

  • 24. [Glaucoma in aniridia(apparent) or irideremia].
    Sampaolesi R; Reca RM
    Arch Oftalmol B Aires; 1968 Mar; 43(3):31-8. PubMed ID: 5737817
    [No Abstract]   [Full Text] [Related]  

  • 25. 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]  

  • 26. [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]  

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

  • 28. Anal atresia, coloboma, microphthalmia, and nasal skin tag in a female patient with 3.5 Mb deletion of 3q26 encompassing SOX2.
    Salem NJ; Hempel M; Heiliger KJ; Hosie S; Meitinger T; Oexle K
    Am J Med Genet A; 2013 Jun; 161A(6):1421-4. PubMed ID: 23613260
    [TBL] [Abstract][Full Text] [Related]  

  • 29. [On the manifestation types of aniridia with reference to a family in Schleswig-Holstein].
    Behnke H; Thiel HJ
    Klin Monbl Augenheilkd; 1967; 151(1):91-8. PubMed ID: 5595985
    [No Abstract]   [Full Text] [Related]  

  • 30. 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]  

  • 31. Renal function evaluation in an adult female with cat-eye syndrome.
    Bellinghieri G; Triolo O; Stella NC; Gemelli M; Musolino R; Monardo P; Savica V
    Am J Nephrol; 1994; 14(1):76-9. PubMed ID: 8017487
    [TBL] [Abstract][Full Text] [Related]  

  • 32. 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]  

  • 33. 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]  

  • 34. 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]  

  • 35. 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]  

  • 36. 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]  

  • 37. Possible autosomal-recessive ocular coloboma.
    Pagon RA; Kalina RE; Lechner DJ
    Am J Med Genet; 1981; 9(3):189-93. PubMed ID: 7282780
    [TBL] [Abstract][Full Text] [Related]  

  • 38. CHROMOSOMES IN COLOBOMA AND ANAL ATRESIA.
    SCHACHENMANN G; SCHMID W; FRACCARO M; MANNINI A; TIEPOLO L; PERONA GP; SARTORI E
    Lancet; 1965 Aug; 2(7406):290. PubMed ID: 14330081
    [No Abstract]   [Full Text] [Related]  

  • 39. Midline facial defects with ocular colobomata.
    Temple IK; Brunner H; Jones B; Burn J; Baraitser M
    Am J Med Genet; 1990 Sep; 37(1):23-7. PubMed ID: 1700608
    [TBL] [Abstract][Full Text] [Related]  

  • 40. 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]  

    [Previous]   [Next]    [New Search]
    of 7.