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 *

123 related articles for article (PubMed ID: 10706355)

  • 1. Growth and developmental retardation, ocular ptosis, cardiac defect, and anal atresia: confirmation of the ROCA-Wiedemann syndrome.
    Zampino G; Balducci F; Mariotti P; Dickmann A; Mastroiacovo P
    Am J Med Genet; 2000 Feb; 90(5):358-60. PubMed ID: 10706355
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Blepharophimosis, ptosis and mental retardation: further delineation of Ohdo syndrome.
    Melnyk AR
    Clin Dysmorphol; 1994 Apr; 3(2):121-4. PubMed ID: 7519949
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Syndrome of mental retardation, cleft palate, eventration of diaphragm, congenital heart defect, glaucoma, growth failure and craniosynostosis.
    Lowry RB; MacLean JR
    Birth Defects Orig Artic Ser; 1977; 13(3B):203-28. PubMed ID: 890093
    [TBL] [Abstract][Full Text] [Related]  

  • 4. New multiple congenital anomalies/mental retardation syndrome with cardio-facio-cutaneous involvement--the CFC syndrome.
    Reynolds JF; Neri G; Herrmann JP; Blumberg B; Coldwell JG; Miles PV; Opitz JM
    Am J Med Genet; 1986 Nov; 25(3):413-27. PubMed ID: 3789005
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Ritscher-Schinzel cranio-cerebello-cardiac (3C) syndrome: report of four new cases and review.
    Leonardi ML; Pai GS; Wilkes B; Lebel RR
    Am J Med Genet; 2001 Aug; 102(3):237-42. PubMed ID: 11484200
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Further delineation of deletion 1p36 syndrome in 60 patients: a recognizable phenotype and common cause of developmental delay and mental retardation.
    Battaglia A; Hoyme HE; Dallapiccola B; Zackai E; Hudgins L; McDonald-McGinn D; Bahi-Buisson N; Romano C; Williams CA; Brailey LL; Zuberi SM; Carey JC
    Pediatrics; 2008 Feb; 121(2):404-10. PubMed ID: 18245432
    [TBL] [Abstract][Full Text] [Related]  

  • 7. 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]  

  • 8. Association of Duane anomaly with mental retardation, cardiac and urinary tract abnormalities: a new autosomal recessive condition?
    Stoll C; Alembik Y; Dott B
    Ann Genet; 1994; 37(4):207-9. PubMed ID: 7710257
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Congenital ptosis and blepharophimosis in a mentally retarded girl: a new case of Ohdo syndrome?
    Rasmussen M; Strømme P
    Clin Dysmorphol; 1998 Jan; 7(1):61-3. PubMed ID: 9546834
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Ohdo-like blepharophimosis syndrome with distinctive facies, neonatal hypotonia, mental retardation and hypoplastic teeth.
    Clayton-Smith J; Krajewska-Walasek M; Fryer A; Donnai D
    Clin Dysmorphol; 1994 Apr; 3(2):115-20. PubMed ID: 8055130
    [TBL] [Abstract][Full Text] [Related]  

  • 11. 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]  

  • 12. Previously apparently undescribed syndrome: shallow orbits, ptosis, coloboma, trigonocephaly, gyral malformations, and mental and growth retardation.
    Ramer JC; Lin AE; Dobyns WB; Winter R; Aymé S; Pallotta R; Ladda RL
    Am J Med Genet; 1995 Jul; 57(3):403-9. PubMed ID: 7545868
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Malpuech facial clefting syndrome in a Japanese boy with cardiac defects.
    Chinen Y; Naritomi K
    Jpn J Hum Genet; 1995 Dec; 40(4):335-8. PubMed ID: 8851768
    [TBL] [Abstract][Full Text] [Related]  

  • 14. The spectrum of congenital cardiac malformations encountered in six children with Kabuki syndrome.
    McMahon CJ; Reardon W
    Cardiol Young; 2006 Feb; 16(1):30-3. PubMed ID: 16454874
    [TBL] [Abstract][Full Text] [Related]  

  • 15. [The Dubowitz syndrome].
    Dumić M; Cvitković M; Letinić D; Filipović-Grcić B; Kordić R
    Lijec Vjesn; 1994; 116(5-6):135-7. PubMed ID: 7968200
    [TBL] [Abstract][Full Text] [Related]  

  • 16. The CFC syndrome--report of the first two cases outside the United States.
    Neri G; Sabatino G; Bertini E; Genuardi M
    Am J Med Genet; 1987 Aug; 27(4):767-71. PubMed ID: 3425595
    [TBL] [Abstract][Full Text] [Related]  

  • 17. A case report of Dubowitz syndrome accompanied by congenital anal atresia.
    Liu J; Zhu T; Zhou S; Xu A
    Int J Dermatol; 2010 Jun; 49(6):684-6. PubMed ID: 20618476
    [No Abstract]   [Full Text] [Related]  

  • 18. [CHARGE association: report of a clinical case with anal atresia and rectovaginal fistula].
    Rodonò A; Romeo MG; Sanges G; Distefano G
    Pediatr Med Chir; 1997; 19(6):469-71. PubMed ID: 9595589
    [TBL] [Abstract][Full Text] [Related]  

  • 19. A boy with choanal atresia and cardiac defect: Burn-McKeown syndrome?
    Toriello HV; Higgins JV
    Clin Dysmorphol; 1999 Apr; 8(2):143-5. PubMed ID: 10319205
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Case report on SHORT syndrome.
    Joo SH; Raygada M; Gibney S; Farzaneh I; Rennert OM
    Clin Dysmorphol; 1999 Jul; 8(3):219-21. PubMed ID: 10457859
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 7.