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 *

80 related articles for article (PubMed ID: 4650397)

  • 41. [Shwachman syndrome (pancreatic insufficiency, neutropenia, metaphyseal dysplasia and dwarfism)].
    Heremans GF; van Gelderen HH
    Ned Tijdschr Geneeskd; 1971 Nov; 115(48):2012-7. PubMed ID: 5148117
    [No Abstract]   [Full Text] [Related]  

  • 42. Genetic skeletal dysplasia in Thailand: the Siriraj experience.
    Wasant P; Waeteekul S; Rimoin DL; Lachman RS
    Southeast Asian J Trop Med Public Health; 1995; 26 Suppl 1():59-67. PubMed ID: 8629144
    [TBL] [Abstract][Full Text] [Related]  

  • 43. Metaphyseal dysostosis.
    Bhargava SK; Pal V
    Indian Pediatr; 1979 Apr; 16(4):371-3. PubMed ID: 511313
    [No Abstract]   [Full Text] [Related]  

  • 44. Additional case of opsismodysplasia supporting autosomal recessive inheritance.
    Beemer FA; Kozlowski KS
    Am J Med Genet; 1994 Feb; 49(3):344-7. PubMed ID: 8209898
    [TBL] [Abstract][Full Text] [Related]  

  • 45. Floating-Harbor syndrome.
    Patton MA; Hurst J; Donnai D; McKeown CM; Cole T; Goodship J
    J Med Genet; 1991 Mar; 28(3):201-4. PubMed ID: 2051457
    [No Abstract]   [Full Text] [Related]  

  • 46. [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]  

  • 47. Developmental orthopaedics. III: Toddlers.
    Bleck EE
    Dev Med Child Neurol; 1982 Aug; 24(4):533-55. PubMed ID: 7117713
    [TBL] [Abstract][Full Text] [Related]  

  • 48. Genetic skeletal dysplasias in the Museum of Pathological Anatomy, Vienna.
    Beighton P; Sujansky E; Patzak B; Portele KA
    Am J Med Genet; 1993 Nov; 47(6):843-7. PubMed ID: 8279481
    [TBL] [Abstract][Full Text] [Related]  

  • 49. Short stature.
    Brook CG
    Practitioner; 1980 Feb; 224(1340):131-8. PubMed ID: 7367364
    [No Abstract]   [Full Text] [Related]  

  • 50. Mosaic supernumerary r(8) syndrome.
    Yilmaz S; Tarkan-Argüden Y; Kuru D; Deviren A; Karaman B; Yüksel A; Hacihanefioğlu S
    Genet Couns; 2005; 16(2):187-90. PubMed ID: 16080301
    [No Abstract]   [Full Text] [Related]  

  • 51. [Hereditary bone dystrophy. Pyknodysostosis].
    Sada Moreno E; Martinez Lage JL; Vazquez Ajuria F; Jimenez Burkhardt A
    Rev Esp Estomatol; 1980; 28(6):331-6. PubMed ID: 6798645
    [No Abstract]   [Full Text] [Related]  

  • 52. 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]  

  • 53. ROENTGEN OBSERVATIONS IN FAMILIAL METAPHYSEAL DYSOSTOSIS.
    MILLER SM; PAUL LW
    Radiology; 1964 Oct; 83():665-73. PubMed ID: 14227699
    [No Abstract]   [Full Text] [Related]  

  • 54. Familial metaphyseal dysplasia.
    Gladney JH; Monteleone PL
    Lancet; 1970 Jul; 2(7662):44-5. PubMed ID: 4194833
    [No Abstract]   [Full Text] [Related]  

  • 55. [Spondylometaphyseal dysostosis. Report on a further case].
    Ludescher E; Kurz R
    Monatsschr Kinderheilkd (1902); 1970 May; 118(5):175-9. PubMed ID: 4999269
    [No Abstract]   [Full Text] [Related]  

  • 56. Skeletal dysplasias.
    Brook CG; de Vries BB
    Arch Dis Child; 1998 Sep; 79(3):285-9. PubMed ID: 9875031
    [No Abstract]   [Full Text] [Related]  

  • 57. An Iranian Patient with Maroteaux Type Acromesomelic Dysplasia, Showing no Involvement of Distal Lower Limbs.
    Moravej H; Moghtaderi M; Mostafavi S
    J Clin Res Pediatr Endocrinol; 2020 Mar; 12(1):122-123. PubMed ID: 31339259
    [No Abstract]   [Full Text] [Related]  

  • 58. Knock knees and bow legs.
    Sharrard WJ
    Br Med J; 1976 Apr; 1(6013):826-7. PubMed ID: 1260352
    [No Abstract]   [Full Text] [Related]  

  • 59. [Detection of hereditary systemic bone diseases in the first year of life].
    Iukina GP; Mikhaĭlova LK
    Pediatriia; 1988; (7):44-8. PubMed ID: 3222120
    [No Abstract]   [Full Text] [Related]  

  • 60. Familial epiphysial dysplasia of the lower limbs.
    WEINBERG H; FRANKEL M; MAKIN M
    J Bone Joint Surg Br; 1960 May; 42-B():313-32. PubMed ID: 13855329
    [No Abstract]   [Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 4.