BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

580 related articles for article (PubMed ID: 8459013)

  • 1. Six generations of a family with multiple limb deficiencies.
    Helal A; Perry T; Ogden JA; Greene TL
    J Pediatr Orthop; 1993; 13(2):210-3. PubMed ID: 8459013
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Counseling dilemmas in EEC syndrome.
    Tekin M; Ohle C; Johnson DE; Christmas JT; Bodurtha J
    Genet Couns; 2000; 11(1):19-24. PubMed ID: 10756423
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Dominant inheritance of syn-camptodactyly of the second and third toes with foot and lower limb asymmetry and scoliosis.
    Halal F
    Am J Med Genet; 1985 Sep; 22(1):149-56. PubMed ID: 4050850
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Autosomal dominant tibial hemimelia-polysyndactyly-triphalangeal thumbs syndrome: report of a Brazilian family.
    Richieri-Costa A; de Miranda E; Kamiya TY; Freire-Maia DV
    Am J Med Genet; 1990 May; 36(1):1-6. PubMed ID: 2333896
    [TBL] [Abstract][Full Text] [Related]  

  • 5. [Townes-Brocks syndrome. Case report and review of the literature].
    Kotzot D; Lorenz P; Bieber A; Gröbe H
    Monatsschr Kinderheilkd; 1992 Jun; 140(6):343-5. PubMed ID: 1640945
    [TBL] [Abstract][Full Text] [Related]  

  • 6. A novel microdeletion at chromosome 2q31.1-31.2 in a three-generation family presenting duplication of great toes with clinodactyly.
    Tsai LP; Liao HM; Chen YJ; Fang JS; Chen CH
    Clin Genet; 2009 May; 75(5):449-56. PubMed ID: 19459884
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Triphalangeal thumb and split foot in the same family.
    Le Marec B; Odent S; Treguier C
    Genet Couns; 1990; 1(3-4):251-8. PubMed ID: 2098049
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Ectrodactyly and absence (hypoplasia) of the tibia: are there dominant and recessive types?
    Majewski E; Goecke T; Meinecke P
    Am J Med Genet; 1996 May; 63(1):185-9. PubMed ID: 8723107
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Further evidence for germinal mosaicism in cleft hand/cleft foot syndrome. Two affected halfsisters and normal father.
    De Smet L; Devriendt K; Fryns JP
    Genet Couns; 2001; 12(3):251-4. PubMed ID: 11693788
    [TBL] [Abstract][Full Text] [Related]  

  • 10. The concurrence of ring constrictions in Adams-Oliver syndrome: additional evidence for vascular disruption as common pathogenetic mechanism.
    Keymolen K; De Smet L; Bracke P; Fryns JP
    Genet Couns; 1999; 10(3):295-300. PubMed ID: 10546102
    [TBL] [Abstract][Full Text] [Related]  

  • 11. [Systematic study of limb anomalies in a population of 35,600 consecutive newborn infants].
    Serville F; Carles D; Frossard AM; Froute F; Rouquier-Toussaint F; Billeaud C
    J Genet Hum; 1982 Dec; 30 Suppl 5():413-22. PubMed ID: 6306159
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Acro-fronto-facio-nasal dysostosis: report of a new Brazilian family.
    Richieri-Costa A; Guion-Almeida ML; Pagnan NA
    Am J Med Genet; 1992 Dec; 44(6):800-2. PubMed ID: 1481850
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Syndactyly type IV/hexadactyly of feet associated with unilateral absence of the tibia.
    Rambaud-Cousson A; Dudin AA; Zuaiter AS; Thalji A
    Am J Med Genet; 1991 Aug; 40(2):144-5. PubMed ID: 1654744
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Inverted insertion of chromosome 7q and ectrodactyly.
    Naritomi K; Izumikawa Y; Tohma T; Hirayama K
    Am J Med Genet; 1993 Jun; 46(5):492-3. PubMed ID: 8322806
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Symbrachydactyly involving hands and feet.
    De Smet L; Fabry G; Fryns JP
    Genet Couns; 1998; 9(1):23-7. PubMed ID: 9555583
    [TBL] [Abstract][Full Text] [Related]  

  • 16. p63 gene analysis in Mexican patients with syndromic and non-syndromic ectrodactyly.
    Berdón-Zapata V; Granillo-Alvarez M; Valdés-Flores M; García-Ortiz JE; Kofman-Alfaro S; Zenteno JC
    J Orthop Res; 2004 Jan; 22(1):1-5. PubMed ID: 14656652
    [TBL] [Abstract][Full Text] [Related]  

  • 17. A novel homozygous missense mutation in WNT10B in familial split-hand/foot malformation.
    Khan S; Basit S; Zimri FK; Ali N; Ali G; Ansar M; Ahmad W
    Clin Genet; 2012 Jul; 82(1):48-55. PubMed ID: 21554266
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Autosomal dominant ectrodactyly and absence of long bones of upper or lower limbs: further clinical delineation.
    Hoyme HE; Jones KL; Nyhan WL; Pauli RM; Robinow M
    J Pediatr; 1987 Oct; 111(4):538-43. PubMed ID: 3655984
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Mutation of HOXA13 in hand-foot-genital syndrome.
    Mortlock DP; Innis JW
    Nat Genet; 1997 Feb; 15(2):179-80. PubMed ID: 9020844
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Mirror hands and feet with a distinct nasal defect, an autosomal dominant condition.
    Martin RA; Jones MC; Jones KL
    Am J Med Genet; 1993 Apr; 46(2):129-31. PubMed ID: 8387244
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 29.