BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

141 related articles for article (PubMed ID: 9689988)

  • 1. Variable phenotype in Kaufman-McKusick syndrome: report of an inbred Muslim family and review of the literature.
    Kumar D; Primhak RA; Kumar A
    Clin Dysmorphol; 1998 Jul; 7(3):163-70. PubMed ID: 9689988
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Popliteal pterygium syndrome. Evidence for a severe autosomal recessive form.
    Bartsocas CS; Papas CV
    J Med Genet; 1972 Jun; 9(2):222-6. PubMed ID: 4339984
    [No Abstract]   [Full Text] [Related]  

  • 3. The Bartsocas-Papas syndrome: autosomal recessive form of popliteal pterygium syndrome in a male infant.
    Papadia F; Zimbalatti F; La Rosa CG
    Am J Med Genet; 1984 Apr; 17(4):841-7. PubMed ID: 6720749
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Autosomal recessive malformation syndrome with minor manifestation in the heterozygotes: a preliminary report of a possible new syndrome.
    Paes-Alves AF; Azevêdo ES; Sousa MG; Almeida-Melo N; Oliveira-Filho OJ
    Am J Med Genet; 1991 Nov; 41(2):141-52. PubMed ID: 1785624
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Familial aplasia/hypoplasia of pelvis, femur, fibula, and ulna with abnormal digits in an inbred Pakistani Muslim family: a possible new autosomal recessive disorder with overlapping manifestations of the syndromes of Fuhrmann, Al-Awadi, and Raas-Rothschild.
    Kumar D; Duggan MB; Mueller RF; Karbani G
    Am J Med Genet; 1997 May; 70(2):107-13. PubMed ID: 9128926
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Newly recognized autosomal recessive faciothoracoskeletal syndrome.
    Richieri-Costa A; Guion-Almeida ML; Lauris JR; Ferreira DM
    Am J Med Genet; 1994 Jan; 49(2):224-8. PubMed ID: 8116673
    [TBL] [Abstract][Full Text] [Related]  

  • 7. An autosomal recessive syndrome of cleft palate, cardiac defect, genital anomalies, and ectrodactyly (CCGE).
    Giannotti A; Digilio MC; Mingarelli R; Dallapiccola B
    J Med Genet; 1995 Jan; 32(1):72-4. PubMed ID: 7897634
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Brief clinical report: autosomal recessive anophthalmia with multiple congenital abnormalities--type Waardenburg.
    Richieri-Costa A; Gollop TR; Otto PG
    Am J Med Genet; 1983 Apr; 14(4):607-15. PubMed ID: 6846395
    [TBL] [Abstract][Full Text] [Related]  

  • 9. [Hydrometrocolpos, polydactylia and congenital heart defect (the McKusick-Dungy-Kaufman syndrome)].
    Hamel BC; ter Haar BG
    Tijdschr Kindergeneeskd; 1984 Aug; 52(4):129-33. PubMed ID: 6495304
    [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. Kaufman oculocerebrofacial syndrome in a girl of 15 years.
    Briscioli V; Manoukian S; Selicorni A; Livini E; Lalatta F
    Am J Med Genet; 1995 Jul; 58(1):21-3. PubMed ID: 7573151
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Autosomal recessive type of whistling face syndrome in twins.
    Kousseff BG; McConnachie P; Hadro TA
    Pediatrics; 1982 Mar; 69(3):328-31. PubMed ID: 7199706
    [TBL] [Abstract][Full Text] [Related]  

  • 13. 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]  

  • 14. Genetics of acheiropodia ("the handless and footless families of Brazil"): XI. Pathologic aspects.
    Marçallo FA; Pilotto RF; Freire-Maia A
    Am J Med Genet; 1979; 4(3):287-91. PubMed ID: 517582
    [TBL] [Abstract][Full Text] [Related]  

  • 15. McKusick-Kaufman syndrome: report of the 66th case complicated by a staphyloma of the left eye.
    Cantani A; Santillo C; Cozzi F
    Padiatr Padol; 1991; 26(4):193-6. PubMed ID: 1749628
    [TBL] [Abstract][Full Text] [Related]  

  • 16. [The Freeman-Sheldon Syndrome].
    Aldinger G; Eulert J
    Z Orthop Ihre Grenzgeb; 1983; 121(5):630-3. PubMed ID: 6649811
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Acheiropody. A report of two cases.
    Kruger LM; Kumar A
    J Bone Joint Surg Am; 1994 Oct; 76(10):1557-60. PubMed ID: 7929505
    [No Abstract]   [Full Text] [Related]  

  • 18. A new recessive syndrome of unusual facies and multiple structural abnormalities.
    Thakker Y; Donnai D
    J Med Genet; 1991 Sep; 28(9):633-5. PubMed ID: 1956065
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Autosomal recessive mode of inheritance of a Coffin-Siris like syndrome.
    Bonioli E; Palmieri A; Bertola A; Bellini C
    Genet Couns; 1995; 6(4):309-12. PubMed ID: 8775417
    [TBL] [Abstract][Full Text] [Related]  

  • 20. 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]  

    [Next]    [New Search]
    of 8.