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 *

91 related articles for article (PubMed ID: 3738402)

  • 21. [Coloboma of iris and choroid in a patient with XYY-syndrome].
    Schwinger E; Wiebusch D
    Klin Monbl Augenheilkd; 1970; 156(6):873-7. PubMed ID: 4988416
    [No Abstract]   [Full Text] [Related]  

  • 22. Wolf-Hirschhorn syndrome with posterior intraorbital coloboma cyst: an unusual case.
    Tutunculer F; Acunas B; Hicdonmez T; Deviren A; Pelitli V
    Brain Dev; 2004 Apr; 26(3):203-5. PubMed ID: 15030910
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Ocular abnormalities in deletion of the long arm of chromosome 11.
    Ferry AP; Marchevsky A; Strauss L
    Ann Ophthalmol; 1981 Dec; 13(12):1373-7. PubMed ID: 6802056
    [No Abstract]   [Full Text] [Related]  

  • 24. [A case of atypical Marfan's syndrome with epilepsy, oligophrenia and coloboma of the iris].
    Klein D; Ionasesco V; Gauthier G; Simona B
    Rev Otoneuroophtalmol; 1969 Nov; 41(7):414-20. PubMed ID: 4994531
    [No Abstract]   [Full Text] [Related]  

  • 25. Congenital hypodontia of maxillary lateral incisors in association with coloboma of the iris and hypomaturation type of amelogenesis imperfecta in a large kindred.
    Atasu M; Eryilmaz A; Genc A; Ozcan M; Ozbayrak S
    J Clin Pediatr Dent; 1997; 21(4):341-55. PubMed ID: 9484124
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Prenatal growth retardation, microcephaly, and eye coloboma in infant with multiple congenital anomalies: further delineation of presumed new dysmorphic syndrome.
    Cuturilo G; Jovanovic I; Vukomanovic G; Djukic M; Stefanovic I; Atanskovic-Markovic M
    Birth Defects Res A Clin Mol Teratol; 2008 Mar; 82(3):166-8. PubMed ID: 18232021
    [TBL] [Abstract][Full Text] [Related]  

  • 27. The significance of atypical colobomata and defects of the iris for the diagnosis of the hereditary aniridia syndrome (author's transl).
    Delleman JW; Winkelman JE
    Klin Monbl Augenheilkd; 1973 Nov; 163(5):528-42. PubMed ID: 4782857
    [No Abstract]   [Full Text] [Related]  

  • 28. [Association of choroidal coloboma, congenital hypertrophy of retinal pigmented epithelium and familial adenomatous polyposis: case report].
    Kermane A; Tachfouti S; El Moussaif H; Mohcine Z
    Bull Soc Belge Ophtalmol; 2004; (292):59-64. PubMed ID: 15253492
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Coloboma of the iris and choroid and retinal detachment in oculo-auricular dysplasia (Goldenhar syndrome).
    Limaye SR
    Eye Ear Nose Throat Mon; 1972 Oct; 51(10):384-6. PubMed ID: 5076735
    [No Abstract]   [Full Text] [Related]  

  • 30. [Syndrome of the 1st branchial arch].
    Morán M
    Cesk Oftalmol; 1973 Mar; 29(2):117-23. PubMed ID: 4694133
    [No Abstract]   [Full Text] [Related]  

  • 31. Distal 11q monosomy syndrome: a report of two Egyptian sibs with normal parental karyotypes confirmed by molecular cytogenetics.
    Afifi HH; Zaki MS; El-Gerzawy AM; Kayed HF
    Genet Couns; 2008; 19(1):47-58. PubMed ID: 18564501
    [TBL] [Abstract][Full Text] [Related]  

  • 32. [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]  

  • 33. [Weill-Marchesani syndrome. Study of a case].
    Jouhaud F; Augustin P; Malbrel C
    Bull Soc Ophtalmol Fr; 1984 Oct; 84(10):1107-11. PubMed ID: 6544165
    [No Abstract]   [Full Text] [Related]  

  • 34. Cytogenetics in ophthalmology.
    Trindade Marques MN; Ferrari F; Cardoso AM; Marques J; Bocchese WT
    Ophthalmic Paediatr Genet; 1985 Aug; 6(1-2):333-8. PubMed ID: 4069594
    [TBL] [Abstract][Full Text] [Related]  

  • 35. 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]  

  • 36. Marker chromosome in cat eye syndrome.
    Verma RS; Babu KA; Rosenfeld W; Jhaveri RC
    Clin Genet; 1985 May; 27(5):526-8. PubMed ID: 3859394
    [No Abstract]   [Full Text] [Related]  

  • 37. New autosomal recessive multiple congenital abnormalities/mental retardation syndrome with craniofacial dysmorphism absent corpus callosum, iris colobomas and connective tissue dysplasia.
    Temtamy SA; Salam MA; Aboul-Ezz EH; Hussein HA; Helmy SA; Shalash BA
    Clin Dysmorphol; 1996 Jul; 5(3):231-40. PubMed ID: 8818452
    [TBL] [Abstract][Full Text] [Related]  

  • 38. 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]  

  • 39. 3:1 meiotic disjunction in a mother with a balanced translocation, 46,XX,t(5,14)(p15;q13) resulting in tertiary trisomy and tertiary monosomy offspring.
    Abeliovich D; Yagupsky P; Bashan N
    Am J Med Genet; 1982 May; 12(1):83-9. PubMed ID: 7091199
    [No Abstract]   [Full Text] [Related]  

  • 40. Dermatoglyphics and chromosomes in cat-eye syndrome.
    Darby CW; Hughes DT
    Br Med J; 1971 Jul; 3(5765):47-8. PubMed ID: 5091903
    [No Abstract]   [Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 5.