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 *

137 related articles for article (PubMed ID: 9409985)

  • 1. [Familial congenital aniridia].
    Zolog I; Belengeanu V; Marinca S; Soim A
    Oftalmologia; 1997; 41(4):326-8. PubMed ID: 9409985
    [TBL] [Abstract][Full Text] [Related]  

  • 2. [Aniridia].
    Liláková D; Hejcmanová D; Jüttnerová V; Rozsíval P
    Cesk Slov Oftalmol; 2002 May; 58(3):176-9. PubMed ID: 12087663
    [TBL] [Abstract][Full Text] [Related]  

  • 3. [Familial occurrence of congenital aniridia].
    Zalewska R; Midro AT; Bakunowicz-Lazarczyk A; Proniewska-Skretek E
    Klin Oczna; 1992; 94(5-6):159-60. PubMed ID: 1453680
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Aniridia associated with ptosis in three generations of the same family.
    Wammanda RD; Idris HW
    Ann Trop Paediatr; 2005 Mar; 25(1):59-62. PubMed ID: 15814051
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Ocular and nonocular findings in patients with aniridia.
    Valenzuela A; Cline RA
    Can J Ophthalmol; 2004 Oct; 39(6):632-8. PubMed ID: 15559649
    [TBL] [Abstract][Full Text] [Related]  

  • 6. [Congenital aniridia].
    Chiruţa D; Stan C
    Oftalmologia; 2014; 58(3):35-40. PubMed ID: 25842623
    [TBL] [Abstract][Full Text] [Related]  

  • 7. A familial syndrome of aniridia and absence of the patella.
    Mirkinson AE; Mirkinson NK
    Birth Defects Orig Artic Ser; 1975; 11(5):129-31. PubMed ID: 1218204
    [TBL] [Abstract][Full Text] [Related]  

  • 8. [Morphological and functional findings in a family with aniridia (author's transl)].
    Weber U; Petersen J
    Klin Monbl Augenheilkd; 1981 Jun; 178(6):439-45. PubMed ID: 6973663
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Polydactyly with ectodermal defect, osteopenia, and mental delay.
    Zannolli R; Buoni S; Viviano M; Macucci F; D'Ambrosio A; Livi W; Mazzei MA; Mazzei F; Sacco P; Volterrani L; Vonella G; Orsi A; Zappella M; Hayek J
    J Child Neurol; 2008 Jun; 23(6):683-9. PubMed ID: 18182642
    [TBL] [Abstract][Full Text] [Related]  

  • 10. A novel CYP1B1 mutation with congenital glaucoma and total aniridia.
    Alzuhairy S; Abu-Amero KK; Al-Shahwan S; Edward DP
    Ophthalmic Genet; 2015 Mar; 36(1):89-91. PubMed ID: 24001018
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Partial aniridia, cerebellar ataxia, and mental deficiency (Gillespie syndrome) in two brothers.
    Wittig EO; Moreira CA; Freire-Maia N; Vianna-Morgante AM
    Am J Med Genet; 1988 Jul; 30(3):703-8. PubMed ID: 3189393
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Clinical manifestations of congenital aniridia.
    Singh B; Mohamed A; Chaurasia S; Ramappa M; Mandal AK; Jalali S; Sangwan VS
    J Pediatr Ophthalmol Strabismus; 2014; 51(1):59-62. PubMed ID: 24369682
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Expanding the neurologic phenotype of oculodentodigital dysplasia in a 4-generation Hispanic family.
    Amador C; Mathews AM; Del Carmen Montoya M; Laughridge ME; Everman DB; Holden KR
    J Child Neurol; 2008 Aug; 23(8):901-5. PubMed ID: 18660473
    [TBL] [Abstract][Full Text] [Related]  

  • 14. [Bilateral congenital aniridia: 5 case reports].
    Laghmari M; Boutimzine N; Abdelouahed AK; Lezrek M; Bensouda N; Benharbit M; Ibrahimy W; Daoudi R; Benchrif Z; Mohcine Z
    J Fr Ophtalmol; 2004 Apr; 27(4):385-91. PubMed ID: 15173647
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Familial transmission of a dysmorphic syndrome: a variant example of Kabuki syndrome?
    Belengeanu V; Rozsnyai K; Farcaş S; Velea I; Fryns JP
    Genet Couns; 2005; 16(2):167-71. PubMed ID: 16080297
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Corneal changes in familial iris coloboma.
    Soong HK; Raizman MB
    Ophthalmology; 1986 Mar; 93(3):335-9. PubMed ID: 3703500
    [TBL] [Abstract][Full Text] [Related]  

  • 17. [A case of Axenfeld's syndrome].
    Markicheva NA; Chistiakova LV; Verkhogliadova GV; Sedova NB
    Vestn Oftalmol; 1991; 107(6):54-6. PubMed ID: 1781127
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Gillespie syndrome, partial aniridia, cerebellar ataxia and mental retardation in mother and daughter.
    Verhulst S; Smet H; Ceulemans B; Geerts Y; Tassignon MJ
    Bull Soc Belge Ophtalmol; 1993; 250():37-42. PubMed ID: 7952360
    [TBL] [Abstract][Full Text] [Related]  

  • 19. DNA diagnosis in a family with autosomal dominant aniridia.
    Verbraak FD; Mannens MA; Redeker EJ; Saunders GF; Bleeker-Wagemakers EM
    Ophthalmic Paediatr Genet; 1991 Dec; 12(4):165-70. PubMed ID: 1815167
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Vertical transmission of the Ohdo blepharophimosis syndrome.
    Mhanni AA; Dawson AJ; Chudley AE
    Am J Med Genet; 1998 May; 77(2):144-8. PubMed ID: 9605288
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 7.