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 *

130 related articles for article (PubMed ID: 1176127)

  • 21. Disorganisation: a case with popliteal pterygia and placental-skin appendages.
    Korniszewski L; Skorka A; Donnai D
    Clin Dysmorphol; 1999 Oct; 8(4):277-81. PubMed ID: 10532177
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Roberts syndrome.
    Qazi A; Qazi SA; Khan MA
    J Pak Med Assoc; 1993 Aug; 43(8):164-6. PubMed ID: 8264097
    [No Abstract]   [Full Text] [Related]  

  • 23. Defects and disabilities of thalidomide children.
    Smithells RW
    Br Med J; 1973 Feb; 1(5848):269-72. PubMed ID: 4631040
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Tetra-amelia and splenogonadal fusion in Roberts syndrome.
    de Ravel TJ; Seftel MD; Wright CA
    Am J Med Genet; 1997 Jan; 68(2):185-9. PubMed ID: 9028456
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Thalidomide experience in Japan.
    Kajii T
    Ann Paediatr; 1965; 205(5):341-54. PubMed ID: 5898604
    [No Abstract]   [Full Text] [Related]  

  • 26. Three siblings with Robert's syndrome.
    Zergollern L; Hitrec F
    Clin Genet; 1976 Apr; 9(4):433-6. PubMed ID: 177235
    [TBL] [Abstract][Full Text] [Related]  

  • 27. [Fèvre-Languepin syndrome. A case description].
    Freiherr von Salis-Soglio G; Dufek P; Froster-Iskenius U
    Z Orthop Ihre Grenzgeb; 1986; 124(2):144-7. PubMed ID: 3716549
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Novel assay for Roberts syndrome assigns variable phenotypes to one complementation group.
    McDaniel LD; Prueitt R; Probst LC; Wilson KS; Tomkins D; Wilson GN; Schultz RA
    Am J Med Genet; 2000 Jul; 93(3):223-9. PubMed ID: 10925387
    [TBL] [Abstract][Full Text] [Related]  

  • 29. [Genetic syndromes of multiple congenital developmental defects].
    Laziuk GI; Lur'e IV; Cherstvoĭ ED
    Arkh Patol; 1977; 39(3):3-11. PubMed ID: 193472
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Studies of malformation syndromes of man XXXXI B: nosologic studies in the Hanhart and the Möbius syndrome.
    Herrmann J; Pallister PD; Gilbert EF; Vieseskul C; Bersu E; Pettersen JC; Opitz JM
    Eur J Pediatr; 1976 Apr; 122(1):19-55. PubMed ID: 1261566
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Genetics of the Meckel syndrome (dysencephalia splanchnocystica).
    Hsia YE; Bratu M; Herbordt A
    Pediatrics; 1971 Aug; 48(2):237-47. PubMed ID: 4997860
    [No Abstract]   [Full Text] [Related]  

  • 32. [Roberts syndrome. Case report and literature review].
    Lazarov N; Sakarski K; Lazarov L
    Akush Ginekol (Sofiia); 2007; 46(2):46-7. PubMed ID: 17469452
    [TBL] [Abstract][Full Text] [Related]  

  • 33. A fetus with upper limb amelia, "caudal regression" and Dandy-Walker defect with an insulin-dependent diabetic mother.
    Bruyere HJ; Viseskul C; Opitz JM; Langer LO; Ishikawa S; Gilbert EF
    Eur J Pediatr; 1980 Aug; 134(2):139-43. PubMed ID: 7439199
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Acromesomelic dwarfism in a child with an interesting family history.
    Borrelli P; Fasanelli S; Marini R
    Pediatr Radiol; 1983; 13(3):165-8. PubMed ID: 6866577
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Malformation complex. Spondylohypoplasia, arthrogryposis, and popliteal pterygium.
    Turkel SB; Iseri AL; Fujimoto AO
    Am J Dis Child; 1980 Jan; 134(1):42-5. PubMed ID: 7350786
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Roberts syndrome.
    Lin MS; Tho CK; Ho NK
    J Singapore Paediatr Soc; 1988; 30(3-4):142-4. PubMed ID: 3216639
    [No Abstract]   [Full Text] [Related]  

  • 37. [The so-called dysmelia syndrome (Thalidomide embryopathy) and its differential diagnosis].
    Weicker H
    Wien Med Wochenschr; 1967 Apr; 117(15):387-90. PubMed ID: 5627596
    [No Abstract]   [Full Text] [Related]  

  • 38. Postaxial acrofacial dysostosis: report on two patients.
    Pereira SC; Rocha CM; Guion-Almeida ML; Richieri-Costa A
    Am J Med Genet; 1992 Oct; 44(3):274-9. PubMed ID: 1488973
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Four cases of amelia of the upper limb associated with anal atresia--is this VACTERL with extreme limb involvement?
    Price SM; Berry AC; Raymond FL; Turnpenny P; Young ID
    Clin Dysmorphol; 1998 Jan; 7(1):35-40. PubMed ID: 9546828
    [TBL] [Abstract][Full Text] [Related]  

  • 40. [Cleft lip, jaw and palate in children with dysmelia].
    Gärtner F; Puls S
    ZWR; 1980 Apr; 89(4):46-50. PubMed ID: 6930781
    [No Abstract]   [Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 7.