BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

148 related articles for article (PubMed ID: 9096751)

  • 1. Digital anomalies, microcephaly, and normal intelligence: new syndrome or Feingold syndrome?
    Kawame H; Pagon RA; Hudgins L
    Am J Med Genet; 1997 Mar; 69(3):240-4. PubMed ID: 9096751
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Feingold syndrome: report of a new family and review.
    Courtens W; Levi S; Verbelen F; Verloes A; Vamos E
    Am J Med Genet; 1997 Nov; 73(1):55-60. PubMed ID: 9375923
    [TBL] [Abstract][Full Text] [Related]  

  • 3. [Feingold syndrome].
    Alessandri JL; Graber D; Tiran-Rajaofera I; Montbrun A; Pilorget H; Samperiz S; Attali T; de Napoli-Cocci S
    Arch Pediatr; 2000 Jun; 7(6):637-40. PubMed ID: 10911531
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Autosomal dominant microcephaly with normal intelligence, short palpebral fissures, and digital anomalies.
    Innis JW; Asher JH; Poznanski AK; Sheldon S
    Am J Med Genet; 1997 Aug; 71(2):150-5. PubMed ID: 9217213
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Imperforate anus in Feingold syndrome.
    Büttiker V; Wojtulewicz J; Wilson M
    Am J Med Genet; 2000 May; 92(3):166-9. PubMed ID: 10817649
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Syndrome of microcephaly, facial and hand abnormalities, tracheoesophageal fistula, duodenal atresia, and developmental delay.
    Feingold M; Hall BD; Lacassie Y; Martínez-Frías ML
    Am J Med Genet; 1997 Mar; 69(3):245-9. PubMed ID: 9096752
    [TBL] [Abstract][Full Text] [Related]  

  • 7. A Feingold syndrome case with previously undescribed features and a new mutation.
    Koçak H; Ozaydin E; Köse G; Marcelis CL; Kamsteeg EJ; Ceylaner S
    Genet Couns; 2009; 20(3):261-7. PubMed ID: 19852433
    [TBL] [Abstract][Full Text] [Related]  

  • 8. How many entities exist for the spectrum of disorders associated with brachydactyly, syndactyly, short stature, microcephaly, and intellectual disability?
    Ravel A; Chouery E; Stora S; Jalkh N; Villard L; Temtamy S; Mégarbané A
    Am J Med Genet A; 2011 Apr; 155A(4):880-4. PubMed ID: 21416592
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Total anonychia congenita and microcephaly with normal intelligence: a new autosomal-recessive syndrome?
    Teebi AS; Kaurah P
    Am J Med Genet; 1996 Dec; 66(3):257-60. PubMed ID: 8985482
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Brachydactylic multiple delta phalanges plus syndrome.
    Ahn CP; Lachman RS; Cox VA; Blumberg B; Klein OD
    Am J Med Genet A; 2005 Sep; 138(1):41-4. PubMed ID: 16092122
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Sandrow syndrome of mirror hands and feet and facial abnormalities.
    Kogekar N; Teebi AS; Vockley J
    Am J Med Genet; 1993 Apr; 46(2):126-8. PubMed ID: 8387243
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Unusual combination of limb malformations in the same patient: brachydactyly with syndactyly and postaxial polydactyly of the hands and postaxial oligodactyly of the feet.
    Ferda Percin E; Yilmaz S
    Clin Dysmorphol; 2003 Oct; 12(4):283-4. PubMed ID: 14564221
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Probable new syndrome in a Mexican family with congenital palmar polyonychia and postaxial limb defects.
    Román Corona-Rivera J; Corona-Rivera E; Fragoso-Herrera R; Nuño-Arana I; Loera-Castañeda V
    Am J Med Genet A; 2004 Mar; 125A(2):205-9. PubMed ID: 14981725
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Feingold syndrome: clinical review and genetic mapping.
    Celli J; van Bokhoven H; Brunner HG
    Am J Med Genet A; 2003 Nov; 122A(4):294-300. PubMed ID: 14518066
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Feingold syndome: a rare but important cause of syndromic tracheoesophageal fistula.
    Layman-Pleet L; Jackson CC; Chou S; Boycott KM
    J Pediatr Surg; 2007 Sep; 42(9):E1-3. PubMed ID: 17848225
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Dominant inheritance of cleft palate with minor abnormalities of hands and feet: a new syndrome?
    Kirk EP; Wilson M
    Clin Dysmorphol; 1999 Jul; 8(3):193-7. PubMed ID: 10457853
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Distal aphalangia, syndactyly, and extra metatarsal, associated with short stature, microcephaly, and borderline intelligence: a new autosomal dominant disorder.
    Martínez-Frías ML; Martín M; Pardo M; Fernandez de las Heras F; Frías JL
    Am J Med Genet; 1995 Jan; 55(2):213-6. PubMed ID: 7717420
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Catel-Manzke syndrome without cleft palate: a case report.
    Puri RD; Phadke SR
    Clin Dysmorphol; 2003 Oct; 12(4):279-81. PubMed ID: 14564220
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Distal aphalangia, an extra metatarsal, short stature and microcephaly: a second case.
    Di Rocco M
    Clin Dysmorphol; 2002 Oct; 11(4):295-6. PubMed ID: 12401998
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Raine syndrome: report of a case with hand and foot anomalies.
    Mahafza T; El-Shanti H; Omari H
    Clin Dysmorphol; 2001 Jul; 10(3):227-9. PubMed ID: 11446420
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 8.