BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

113 related articles for article (PubMed ID: 1789638)

  • 21. [Unusual syndrome with acceleration of skeletal maturation (Marshall's syndrome). 1st case in the Italian literature].
    De Toni E; Duillo MT; De Toni T; Cortese M; Bergamo F
    Minerva Pediatr; 1976 Jul; 28(24):1499-509. PubMed ID: 1012192
    [No Abstract]   [Full Text] [Related]  

  • 22. [Differentiation between developmental bone diseases in VACTERL abnormalities and in the TAR syndrome].
    Ludányi I
    Orv Hetil; 1986 Dec; 127(52):3220. PubMed ID: 3808700
    [No Abstract]   [Full Text] [Related]  

  • 23. [Schwartz-Jampel syndrome type 2 versus Stüve-Wiedemann syndrome].
    Navarrete Faubel FE; Pérez Aytés A; Pastor Rosado J; Mascarell Gregoria A
    An Esp Pediatr; 2002 May; 56(5):473-4. PubMed ID: 12042125
    [No Abstract]   [Full Text] [Related]  

  • 24. A suggested mode of pigment transfer into the dermis.
    Guerrier C
    Acta Derm Venereol; 1973; 53(3):173-7. PubMed ID: 4124006
    [No Abstract]   [Full Text] [Related]  

  • 25. Frontometaphyseal dysplasia: a progressive disease of bone and connective tissue.
    Danks DM; Mayne V
    Birth Defects Orig Artic Ser; 1974; 10(12):57-60. PubMed ID: 4282264
    [No Abstract]   [Full Text] [Related]  

  • 26. Stapedotomy in Larsen's syndrome.
    Horn KL; Pai V; Beauparlant PA
    Am J Otol; 1990 May; 11(3):205-6. PubMed ID: 2343906
    [No Abstract]   [Full Text] [Related]  

  • 27. [The VATER syndrome in a 2-and-half-year-old girl].
    Seemanová E; Sevcíková M; Tosovský V
    Cesk Pediatr; 1979 May; 34(5):291-2. PubMed ID: 445665
    [No Abstract]   [Full Text] [Related]  

  • 28. Incontinentia pigmenti. A case report.
    Felt SE; Jacobs DS
    J Kans Med Soc; 1973 Feb; 74(2):43-5. PubMed ID: 4631553
    [No Abstract]   [Full Text] [Related]  

  • 29. [The diversities of Phacomatosis (Hamartosis). Apropos of a case likely to represent a new syndrome].
    Carlier G; Lambotte C; Pierard G
    Arch Fr Pediatr; 1974; 31(7):657-68. PubMed ID: 4217147
    [No Abstract]   [Full Text] [Related]  

  • 30. [Dyskeratosis congenita with thrombopenia; its relation with Fanconi's anemia: a case].
    Barrière H
    Sem Hop; 1970 Nov; 46(47):3083-7. PubMed ID: 4344185
    [No Abstract]   [Full Text] [Related]  

  • 31. Patient presentation.
    Feingold M; Bull MJ; Darling DB
    Birth Defects Orig Artic Ser; 1974; 10(7):87-91. PubMed ID: 4419732
    [No Abstract]   [Full Text] [Related]  

  • 32. Invited editorial comment on "restrictive dermopathy" and report of another case.
    Toriello HV
    Birth Defects Orig Artic Ser; 1988; 24(2):103-8. PubMed ID: 3179423
    [No Abstract]   [Full Text] [Related]  

  • 33. Congenital fascial dystrophy: stiff skin syndrome--a human counterpart of the tight-skin mouse.
    Jablonska S; Schubert H; Kikuchi I
    J Am Acad Dermatol; 1989 Nov; 21(5 Pt 1):943-50. PubMed ID: 2808830
    [TBL] [Abstract][Full Text] [Related]  

  • 34. [Case report on incontinentia pigmenti or Bloch-Sulzberger syndrome].
    Maione M; Mammarella E
    Ann Ottalmol Clin Ocul; 1971 Mar; 97(3):55-70. PubMed ID: 5004456
    [No Abstract]   [Full Text] [Related]  

  • 35. MR imaging of congenital/developmental and acquired disorders of the pediatric hip and pelvis.
    Dillon JE; Connolly SA; Connolly LP; Kim YJ; Jaramillo D
    Magn Reson Imaging Clin N Am; 2005 Nov; 13(4):783-97. PubMed ID: 16275584
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Marshall-Smith syndrome: two case reports and a review of pulmonary manifestations.
    Johnson JP; Carey JC; Glassy FJ; Paglieroni T; Lipson MH
    Pediatrics; 1983 Feb; 71(2):219-23. PubMed ID: 6823423
    [TBL] [Abstract][Full Text] [Related]  

  • 37. [A clinical case of tricho-dento-osseous syndrome].
    Lolli R; Addessi G; Valgiusti C
    Riv Odontostomatol Implantoprotesi; 1984; (2):29-32. PubMed ID: 6595591
    [No Abstract]   [Full Text] [Related]  

  • 38. Differential diagnosis of pachydermoperiostosis.
    Verhoeve L; Degreef H; Marchal G; Staessen J
    Arch Belg Dermatol; 1974; 30(4):209-13. PubMed ID: 4469416
    [No Abstract]   [Full Text] [Related]  

  • 39. The Winchester syndrome: (a case report).
    Irani A; Shah BN; Merchant RH
    Indian Pediatr; 1978 Oct; 15(10):861-3. PubMed ID: 730313
    [No Abstract]   [Full Text] [Related]  

  • 40. Lentiginosis profusa syndrome (multiple lentigines syndrome).
    Selmanowitz VJ; Orentreich N; Felsenstein JM
    Arch Dermatol; 1971 Oct; 104(4):393-401. PubMed ID: 5000391
    [No Abstract]   [Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 6.