BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

646 related articles for article (PubMed ID: 19250421)

  • 1. Café au lait macules and cerebro-oculo-facio-skeletal syndrome: a novel association.
    Twede JV; Difazio M
    Pediatr Dermatol; 2009; 26(1):97-9. PubMed ID: 19250421
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Cerebro-oculo-facio-skeletal syndrome: further delineation.
    Gershoni-Baruch R; Ludatscher RM; Lichtig C; Sujov P; Machoul I
    Am J Med Genet; 1991 Oct; 41(1):74-7. PubMed ID: 1951466
    [TBL] [Abstract][Full Text] [Related]  

  • 3. 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]  

  • 4. Cerebro-oculo-facio-skeletal (COFS) syndrome. The variability of presenting symptoms as a manifestation of two subtypes?
    Casteels I; Wijnants A; Casaer P; Eggermont E; Misotten L; Fryns JP
    Genet Couns; 1991; 2(1):43-6. PubMed ID: 1741976
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Cerebro-oculo-facio-skeletal syndrome: report of two cases from Turkey with postmortem findings.
    Semerci CN; Onat N; Günçe S; Demirel N; Yilmazer MB; Oznur I; Türkyilmaz C; Balci S
    Turk J Pediatr; 2002; 44(3):269-73. PubMed ID: 12405446
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Muscle involvement in the cerebro-oculo-facio-skeletal syndrome.
    Longman C; Sewry CA; Muntoni F
    Pediatr Neurol; 2004 Feb; 30(2):125-8. PubMed ID: 14984906
    [TBL] [Abstract][Full Text] [Related]  

  • 7. 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]  

  • 8. The diagnostic and clinical significance of café-au-lait macules.
    Shah KN
    Pediatr Clin North Am; 2010 Oct; 57(5):1131-53. PubMed ID: 20888463
    [TBL] [Abstract][Full Text] [Related]  

  • 9. The first case of Niikawa-Kuroki syndrome in Kazakhstan associated with café au lait spots.
    Al Mosawi AJ; Fewin L
    G Ital Dermatol Venereol; 2009 Oct; 144(5):613-5. PubMed ID: 19834439
    [TBL] [Abstract][Full Text] [Related]  

  • 10. A girl with cutaneous hyperpigmentation, café au lait spots and ring chromosome 15 without significant deletion.
    Morava E; Bartsch O; Czako M; Frensel A; Kárteszi J; Kosztolányi GY
    Genet Couns; 2003; 14(3):337-42. PubMed ID: 14577679
    [TBL] [Abstract][Full Text] [Related]  

  • 11. [Cerebro-oculo-facio-skeletal (COFS) syndrome].
    Kosuga M; Okuyama T
    Ryoikibetsu Shokogun Shirizu; 2000; (30 Pt 5):49-50. PubMed ID: 11057139
    [No Abstract]   [Full Text] [Related]  

  • 12. Recurrent Fraser syndrome.
    Kiran G; Namita G; Dheeraj S
    Prenat Diagn; 2007 Feb; 27(2):184-5. PubMed ID: 17266165
    [No Abstract]   [Full Text] [Related]  

  • 13. Megalocornea and mental retardation syndrome: a new case.
    Grønbech-Jensen M
    Am J Med Genet; 1989 Apr; 32(4):468-9. PubMed ID: 2672814
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Fraser syndrome with bladder pseudoexstrophy.
    Daia JA
    Saudi Med J; 2001 May; 22(5):455-6. PubMed ID: 11376391
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Possible new autosomal recessive syndrome of partial agenesis of the corpus callosum, pontine hypoplasia, focal white matter changes, hypotonia, mental retardation, and minor anomalies.
    Jonas RE; Kimonis VE; Morales A
    Am J Med Genet; 1997 Dec; 73(2):184-8. PubMed ID: 9409870
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Neurofibromatosis type 1 with overlap Turner syndrome and Klinefelter syndrome.
    Hatipoglu N; Kurtoglu S; Kendirci M; Keskin M; Per H
    J Trop Pediatr; 2010 Feb; 56(1):69-72. PubMed ID: 19578129
    [TBL] [Abstract][Full Text] [Related]  

  • 17. 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]  

  • 18. Cutaneous features associated with microcephalic osteodysplastic primordial dwarfism type II.
    Webber N; O'Toole EA; Paige DG; Rosser E
    Pediatr Dermatol; 2008; 25(3):401-2. PubMed ID: 18577061
    [TBL] [Abstract][Full Text] [Related]  

  • 19. 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]  

  • 20. A familial syndrome with hypotonia, mental retardation and dysmorphic features resembling Cohen syndrome.
    Mejía-Baltodano G; Bobadilla L; Solís A; Mendoza R; Díaz-Gallardo MY; Barros-Núñez P
    Genet Couns; 1997; 8(4):311-6. PubMed ID: 9457500
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 33.