BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

311 related articles for article (PubMed ID: 16080293)

  • 1. A novel Fryns "Anophthalmia-plus" syndrome associated with primary hypothyroidism.
    Akalin I; Senses DA; Ilgin-Ruhi H; Misirlioğlu E; Yalçiner M; Cetinkaya E; Fryns JP; Tükün A
    Genet Couns; 2005; 16(2):145-8. PubMed ID: 16080293
    [TBL] [Abstract][Full Text] [Related]  

  • 2. [Fryns syndrome. Report on 3 new cases].
    Alessandri JL; Attali T; Brayer C; Dupuy L; Pilorget H; Ramful D; Samperiz S; Tiran-Rajaofera I; Robin S
    Arch Pediatr; 2007 Jul; 14(7):903-7. PubMed ID: 17442547
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Fryns anophthalmia-plus syndrome with hypoplastic adrenal glands.
    Ozalp O; Ozcimen EE; Yilmaz Z; Yanik F; Sahin FI
    Genet Couns; 2008; 19(1):43-6. PubMed ID: 18564500
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Malpuech syndrome: a possible relationship with the Wolf-Hirschhorn/Pitt-Roger-Danks phenotype.
    Selicorni A; Faravelli F
    Am J Med Genet; 2000 Nov; 95(3):291. PubMed ID: 11102941
    [No Abstract]   [Full Text] [Related]  

  • 5. Apparently new "anophthalmia-plus" syndrome in sibs.
    Fryns JP; Legius E; Moerman P; Vandenberghe K; Van den Berghe H
    Am J Med Genet; 1995 Aug; 58(2):113-4. PubMed ID: 8533799
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Anophthalmia, cleft lip/palate, absent vomer bone, nystagmus, and mental-motor retardation: a new syndrome or Fryns "anophthalmia-plus" syndrome?
    Ozçelik D; Sağlam I; SIlan F; Sezen G; Unveren T
    Cleft Palate Craniofac J; 2008 May; 45(3):256-60. PubMed ID: 18452356
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Joubert syndrome associated with patent ductus arteriosus in a newborn infant.
    Peker E; Kirimi E; Sal E; Ceylan A; Ustyol L; Caksen H
    Genet Couns; 2009; 20(3):289-92. PubMed ID: 19852437
    [No Abstract]   [Full Text] [Related]  

  • 8. Acro-cardio-facial syndrome associated with neuroepithelial cyst: a case report.
    Sivasli O; Ozer EA; Ozer A; Aydinlioglu H; Helvaci M
    Genet Couns; 2007; 18(2):247-50. PubMed ID: 17710878
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Brief clinical report: autosomal recessive anophthalmia with multiple congenital abnormalities--type Waardenburg.
    Richieri-Costa A; Gollop TR; Otto PG
    Am J Med Genet; 1983 Apr; 14(4):607-15. PubMed ID: 6846395
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Fryns anophthalmia-plus syndrome: two rare cases.
    Bozkurt O; Bidev D; Sari FN; Dizdar EA; Ulu HO; Uras N; Oguz SS; Canpolat FE; Dilmen U
    Genet Couns; 2014; 25(4):395-8. PubMed ID: 25804017
    [TBL] [Abstract][Full Text] [Related]  

  • 11. A collodion baby with hypothyroidism.
    Dogan DG; Aslan M; Karabiber H
    Genet Couns; 2010; 21(3):343-6. PubMed ID: 20964127
    [TBL] [Abstract][Full Text] [Related]  

  • 12. A lethal, unclassifiable form of micromelic dwarfism with posterior cleft palate, multiple cervicothoracal vertebral anomalies and iliac hypoplasia: evidence for autosomal recessive inheritance.
    Fryns JP; Moerman P
    Genet Couns; 1998; 9(1):61-2. PubMed ID: 9555592
    [No Abstract]   [Full Text] [Related]  

  • 13. An/micr-ophthalmia, cleft lip/palate, and short limbs: a new syndrome simulating a short rib syndrome.
    Kariminejad A; Ghaderi-Sohi S; Kariminejad MH; Lachman R
    Fetal Pediatr Pathol; 2012 Oct; 31(5):295-9. PubMed ID: 22432872
    [TBL] [Abstract][Full Text] [Related]  

  • 14. [Genetic morphological fatal syndromes. The cryptophthalmos syndrome (Fraser syndrome)].
    Henkel KE; Pfeiffer RA; Stöss H
    Pathologe; 1993 Mar; 14(2):94-5. PubMed ID: 8469653
    [No Abstract]   [Full Text] [Related]  

  • 15. An intermediate phenotype between Hay-Wells and Rapp-Hodgkin syndromes in a patient with a novel P63 mutation: confirmation of a variable phenotypic spectrum with a common aetiology.
    Prontera P; Escande F; Cocchi G; Donti E; Martini A; Sensi A
    Genet Couns; 2008; 19(4):397-402. PubMed ID: 19239083
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Anophthalmia-plus syndrome with unusual findings. A clinical report and review of the literature.
    Cayir A; Tasdemir S; Eroz R; Yuce I; Orbak Z; Tatar A
    Genet Couns; 2013; 24(3):307-12. PubMed ID: 24341146
    [TBL] [Abstract][Full Text] [Related]  

  • 17. [Congenital anophthalmias: a case of trisomy 13].
    Kouassi FX; Koffi KV; Safede K; Cochard C; Cochener B
    J Fr Ophtalmol; 2006 Apr; 29(4):e10. PubMed ID: 16885798
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Fryns syndrome.
    Stratton RF; Young RS; Heiman HS; Carter JM
    Am J Med Genet; 1993 Mar; 45(5):562-4. PubMed ID: 8456824
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Sporadic congenital malformations of newborn inbred mice.
    Kalter H
    Teratology; 1968 May; 1(2):193-9. PubMed ID: 5759135
    [No Abstract]   [Full Text] [Related]  

  • 20. Complicated anophthalmos.
    Bajwa GS; Thapar K; Dhawan AK; Kapoor A
    Indian Pediatr; 1995 Apr; 32(4):480-2. PubMed ID: 8635814
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 16.