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 *

455 related articles for article (PubMed ID: 17266165)

  • 21. Sclerocornea, hypertelorism, syndactyly, and ambiguous genitalia.
    Martínez-Frías ML; Bermejo E; Sánchez Otero T; Urioste M; Morena V; Cruz E
    Am J Med Genet; 1994 Jan; 49(2):195-7. PubMed ID: 8116666
    [TBL] [Abstract][Full Text] [Related]  

  • 22. [An anatomical study of familial cryptophthalmos].
    Emberger JM; Taib J; Caderas de Kerleau J; Pincemin D
    J Genet Hum; 1976 Nov; 24 Suppl():23-9. PubMed ID: 192847
    [No Abstract]   [Full Text] [Related]  

  • 23. Bilateral orbito-palpebral cysts in a case of cryptophthalmos associated with Fraser syndrome.
    Mocan MC; Ozgen B; Irkec M
    J AAPOS; 2008 Apr; 12(2):210-1. PubMed ID: 18083592
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Fraser syndrome (cryptophthalmos [hidden eye]-syndactyly syndrome).
    Sarman G; Speer ME; Rudolph AJ
    J Perinatol; 1995; 15(6):503-6. PubMed ID: 8648460
    [No Abstract]   [Full Text] [Related]  

  • 25. Prenatal diagnosis and intrafamilial clinical heterogeneity of Fraser syndrome.
    Rousseau T; Laurent N; Thauvin-Robinet C; Lionnais S; Durand C; Faivre L; Sagot P
    Prenat Diagn; 2002 Aug; 22(8):692-6. PubMed ID: 12210578
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Bartsocas-Papas syndrome.
    Godbole K; Bhide V; Godbole G
    Indian Pediatr; 2008 Sep; 45(9):780-2. PubMed ID: 18820389
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Fraser syndrome and cryptophthalmos: review of the diagnostic criteria and evidence for phenotypic modules in complex malformation syndromes.
    Slavotinek AM; Tifft CJ
    J Med Genet; 2002 Sep; 39(9):623-33. PubMed ID: 12205104
    [TBL] [Abstract][Full Text] [Related]  

  • 28. [Fraser syndrome: frequency in our environment and clinical-epidemiological aspects of a consecutive series of cases].
    Martínez-Frías ML; Bermejo Sánchez E; Félix V; Calvo Celada R; Ayala Garcés A; Hernández Ramón F
    An Esp Pediatr; 1998 Jun; 48(6):634-8. PubMed ID: 9662850
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Asphyxiating thoracic dystrophy and syndactyly of the toes in a newborn: coincidence or a new association?
    Tastekin A; Polat P; Ors R
    Genet Couns; 2003; 14(1):113-4. PubMed ID: 12725597
    [No Abstract]   [Full Text] [Related]  

  • 30. Oculo-dento-digital dysplasia (OMIM *164200). Full manifestation of the syndrome in a 9.5 year-old girl and type III syndactyly in the father.
    Ioan DM; Dagomiz D; Fryns JP
    Genet Couns; 2002; 13(2):187-9. PubMed ID: 12150221
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Novel GJA1 mutations in patients with oculo-dento-digital dysplasia (ODDD).
    Debeer P; Van Esch H; Huysmans C; Pijkels E; De Smet L; Van de Ven W; Devriendt K; Fryns JP
    Eur J Med Genet; 2005; 48(4):377-87. PubMed ID: 16378922
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Mental retardation, obesity, mandibular prognathism with eye and skin anomalies (MOMES syndrome): a newly recognized autosomal recessive syndrome.
    Kantaputra PN; Kunachaichote J; Patikulsila P
    Am J Med Genet; 2001 Nov; 103(4):283-8. PubMed ID: 11746007
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Central nervous system abnormalities in oculodentodigital dysplasia.
    Schrander-Stumpel CT; Franke CL
    Genet Couns; 1996; 7(3):233-5. PubMed ID: 8897047
    [No Abstract]   [Full Text] [Related]  

  • 34. Neonatal death in Marshall-Smith syndrome.
    Chatel C; Maazoul F; Sigaudy S; Fredouille C; Ayme S; Philip N
    Genet Couns; 1998; 9(1):15-8. PubMed ID: 9555581
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Cerebro-oculo-facio-skeletal (COFS) syndrome in siblings.
    Kulkarni ML; Sehgal A; Keshavamurthy KS; Kulkarni PM
    Indian J Pediatr; 2004 Dec; 71(12):e56-7. PubMed ID: 15630331
    [TBL] [Abstract][Full Text] [Related]  

  • 36. 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]  

  • 37. 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]  

  • 38. Prenatal sonographic appearance of cryptophthalmos in Fraser syndrome.
    Vijayaraghavan SB; Suma N; Lata S; Kamakshi K
    Ultrasound Obstet Gynecol; 2005 Jun; 25(6):629-30. PubMed ID: 15909316
    [No Abstract]   [Full Text] [Related]  

  • 39. Mutchinick syndrome in a Japanese girl.
    Tonoki H; Hattori T; Kamoshida H; Ohta Y; Niikawa N
    Am J Med Genet; 1999 Mar; 83(2):96-9. PubMed ID: 10190479
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Prenatal detection of Fraser syndrome without cryptophthalmos: case report and review of the literature.
    Berg C; Geipel A; Germer U; Pertersen-Hansen A; Koch-Dörfler M; Gembruch U
    Ultrasound Obstet Gynecol; 2001 Jul; 18(1):76-80. PubMed ID: 11489232
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 23.