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 *

162 related articles for article (PubMed ID: 8725790)

  • 21. Cardio-facio-cutaneous syndrome: a case report.
    Ribeiro de Castro MC; de Aquino AM; Camilo C; Maceira JP; Ramos-e-Silva M
    Int J Dermatol; 2002 Dec; 41(12):923-5. PubMed ID: 12492991
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Two female siblings with a previously unreported MCA/MR syndrome: pre- and postnatal growth retardation, iris colobomata, spasticity, facial dysmorphism and dilated ventricles.
    Yüksel A; Seven M; Deviren A; Söylemez MA; Hacihanefioğlu S; Ulutin T; Cenani A
    Genet Couns; 1999; 10(3):265-9. PubMed ID: 10546098
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Cardio-facio-cutaneous (CFC) syndrome--a distinct entity? Report of three patients demonstrating the diagnostic difficulties in delineation of CFC syndrome.
    Wieczorek D; Majewski F; Gillessen-Kaesbach G
    Clin Genet; 1997 Jul; 52(1):37-46. PubMed ID: 9272711
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Fine mapping of Noonan/cardio-facio cutaneous syndrome in a large family.
    Legius E; Schollen E; Matthijs G; Fryns JP
    Eur J Hum Genet; 1998 Jan; 6(1):32-7. PubMed ID: 9781012
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Dubowitz syndrome: long-term follow-up of an original patient.
    Hansen KE; Kirkpatrick SJ; Laxova R
    Am J Med Genet; 1995 Jan; 55(2):161-4. PubMed ID: 7536394
    [TBL] [Abstract][Full Text] [Related]  

  • 26. [Trichorhinophalangeal syndrome. Apropos of a case].
    Marchand C; Villedieu MH; Plauchu H; Rigot-Muller G; Chouvet B
    Ann Dermatol Venereol; 1985; 112(12):973-80. PubMed ID: 3833045
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Diabetes mellitus, mental retardation, lipodystrophy and dysmorphic traits.
    Verloes A; Ernould C; Dubru JM; Malchair R; Koulischer L
    Clin Dysmorphol; 1994 Apr; 3(2):160-3. PubMed ID: 8055137
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Cardio-facio cutaneous syndrome: neurological manifestations.
    Gross-Tsur V; Gross-Kieselstein E; Amir N
    Clin Genet; 1990 Nov; 38(5):382-6. PubMed ID: 2149308
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Neurologic and gastrointestinal dysfunction in cardio-facio-cutaneous syndrome: identification of a severe phenotype.
    Grebe TA; Clericuzio C
    Am J Med Genet; 2000 Nov; 95(2):135-43. PubMed ID: 11078563
    [TBL] [Abstract][Full Text] [Related]  

  • 30. 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]  

  • 31. The cardio-facio-cutaneous syndrome: a long-term follow-up of two patients, with special reference to the neurological features.
    Sabatino G; Verrotti A; Domizio S; Angeiozzi B; Chiarelli F; Neri G
    Childs Nerv Syst; 1997 Apr; 13(4):238-41. PubMed ID: 9202862
    [TBL] [Abstract][Full Text] [Related]  

  • 32. [9p-syndrome].
    Fujita H
    Ryoikibetsu Shokogun Shirizu; 2000; (30 Pt 5):318-9. PubMed ID: 11057244
    [No Abstract]   [Full Text] [Related]  

  • 33. Seckel syndrome with polyarteritis nodosa.
    Kutlu R; Alkan A; Kutlu O; Yakinci C
    Indian Pediatr; 2004 Nov; 41(11):1158-61. PubMed ID: 15591669
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Costello syndrome and facio-cutaneous-skeletal syndrome.
    Philip N; Mancini J
    Am J Med Genet; 1993 Aug; 47(2):174-5. PubMed ID: 8213902
    [No Abstract]   [Full Text] [Related]  

  • 35. [FG syndrome].
    Kato R
    Ryoikibetsu Shokogun Shirizu; 2000; (30 Pt 5):182-3. PubMed ID: 11057188
    [No Abstract]   [Full Text] [Related]  

  • 36. Facio-cardio-renal (Eastman-Bixler) syndrome.
    Nevin NC; Hill AE; Carson DJ
    Am J Med Genet; 1991 Jul; 40(1):31-3. PubMed ID: 1887846
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Expansion of the phenotype in Hennekam syndrome: a case with new manifestations.
    Angle B; Hersh JH
    Am J Med Genet; 1997 Aug; 71(2):211-4. PubMed ID: 9217224
    [TBL] [Abstract][Full Text] [Related]  

  • 38. [Partial trisomy 10q syndrome].
    Imaizumi K
    Ryoikibetsu Shokogun Shirizu; 2000; (30 Pt 5):325-6. PubMed ID: 11057247
    [No Abstract]   [Full Text] [Related]  

  • 39. [Trisomy 8 mosaic syndrome].
    Hada S; Abe T
    Ryoikibetsu Shokogun Shirizu; 2000; (30 Pt 5):316-7. PubMed ID: 11057243
    [No Abstract]   [Full Text] [Related]  

  • 40. Further delineation of Costello syndrome.
    Teebi AS; Shaabani IS
    Am J Med Genet; 1993 Aug; 47(2):166-8. PubMed ID: 8213898
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 9.