BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

181 related articles for article (PubMed ID: 5006211)

  • 21. The Dyggve-Melchior-Clausen syndrome in Indian siblings.
    Winship WS; Rubin DL
    Clin Genet; 1992 Nov; 42(5):240-5. PubMed ID: 1486701
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Atlantoaxial Instability Treated with Posterior Atlantoaxial Fixation in Two Siblings with Dyggve-Melchior-Clausen Syndrome.
    Shah A; Bhambere S; Ranjan S; Dandpat S; Goel A
    Turk Neurosurg; 2020; 30(6):956-960. PubMed ID: 33216345
    [TBL] [Abstract][Full Text] [Related]  

  • 23. [Dyggve-Melchior-Clausen syndrome: differential diagnosis of mucopolysaccharidosis type IV or Morquio disease].
    Coëslier A; Boute-Bénéjean O; Moerman A; Fron D; Manouvrier-Hanu S
    Arch Pediatr; 2001 Aug; 8(8):838-42. PubMed ID: 11524915
    [TBL] [Abstract][Full Text] [Related]  

  • 24. The Dyggve-Melchior-Clausen syndrome.
    Rastogi SC; Clausen J; Melchior JC; Dyggve HV
    Clin Chim Acta; 1977 Jul; 78(1):55-69. PubMed ID: 141987
    [No Abstract]   [Full Text] [Related]  

  • 25. [Dyggve-Melchior-Clausen syndrome: presentation of a case with a mutation of possible Spanish origin].
    Martínez-Frías ML; Cormier-Daire V; Cohn DH; Mendioroz J; Bermejo E; Mansilla E
    Med Clin (Barc); 2007 Feb; 128(4):137-40. PubMed ID: 17288936
    [TBL] [Abstract][Full Text] [Related]  

  • 26. [Dyggve-Melchior-Clausen syndrome, diagnostic difficulty due to it similarity to Morquio disease].
    Rodríguez Rodríguez CM; Pineda Marfa M; Duque R; Cormier-Daire V
    Neurologia; 2007 Mar; 22(2):126-9. PubMed ID: 17323241
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Bilateral Severe Genu Varum in Dyggve-Melchior-Clausen Syndrome - A Case Report.
    Yadav AK; Wadia F; Gawhale S; Panchal S; Talukder P; Mokashi M
    J Orthop Case Rep; 2021 Aug; 11(8):84-86. PubMed ID: 35004383
    [TBL] [Abstract][Full Text] [Related]  

  • 28. The Dyggve-Melchior-Clausen (DMC) syndrome. A 15 year follow-up and a survey of the present clinical and chemical findings.
    Dyggve HV; Melchior JC; Clausen J; Rastogi SC
    Neuropadiatrie; 1977 Nov; 8(4):429-42. PubMed ID: 579440
    [TBL] [Abstract][Full Text] [Related]  

  • 29. [Dyggve-Melchior-Clausen syndrome. Case report and review of the literature].
    Schlaepfer R; Rampini S; Wiesmann U
    Helv Paediatr Acta; 1981; 36(6):543-59. PubMed ID: 7037691
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Case report 431: Dyggve-Melchior-Clausen syndrome (DMCS).
    Hall-Craggs MA; Chapman M
    Skeletal Radiol; 1987; 16(5):422-4. PubMed ID: 3114890
    [No Abstract]   [Full Text] [Related]  

  • 31. Dyggve-Melchior-Clausen dysplasia. Morphological and biochemical findings in cartilage growth zones.
    Engfeldt B; Bui TH; Eklöf O; Hjerpe A; Reinholt FP; Ritzen EM; Wikström B
    Acta Paediatr Scand; 1983 Mar; 72(2):269-74. PubMed ID: 6404126
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Abnormal serum alpha 2-macroglobulin in Dyggve-Melchior-Clausen syndrome.
    Rastogi SC; Clausen J; Melchior JC; Dyggve HV
    J Clin Chem Clin Biochem; 1980 Jan; 18(1):67-8. PubMed ID: 6153699
    [TBL] [Abstract][Full Text] [Related]  

  • 33. A homozygous nonsense variant in DYM underlies Dyggve-Melchior-Clausen syndrome associated with ectodermal features.
    Abdullah ; Shah PW; Nawaz S; Hussain S; Ullah A; Basit S; Ahmad W
    Mol Biol Rep; 2020 Sep; 47(9):7083-7088. PubMed ID: 32886330
    [TBL] [Abstract][Full Text] [Related]  

  • 34. [Dyggve-Melchior-Clausen syndrome: 2 cases of ours].
    Frediani P; Capilupi B; Kunzle AL; Brunelli PC; Maruffi G
    Chir Organi Mov; 1988; 73(4):379-83. PubMed ID: 3251711
    [No Abstract]   [Full Text] [Related]  

  • 35. A recurrent mutation in Moroccan patients with Dyggve-Melchior-Clausen syndrome: Report of a new case and review.
    Elalaoui SC; Mariam T; Ilham R; Yassamine D; Abdelaziz S
    Indian J Hum Genet; 2011 May; 17(2):97-9. PubMed ID: 22090722
    [TBL] [Abstract][Full Text] [Related]  

  • 36. The Dyggve-Melchior-Clausen syndrome.
    Naffah J
    Am J Hum Genet; 1976 Nov; 28(6):607-14. PubMed ID: 1008064
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Homozygosity mapping of a Dyggve-Melchior-Clausen syndrome gene to chromosome 18q21.1.
    Thauvin-Robinet C; El Ghouzzi V; Chemaitilly W; Dagoneau N; Boute O; Viot G; Mégarbané A; Sefiani A; Munnich A; Le Merrer M; Cormier-Daire V
    J Med Genet; 2002 Oct; 39(10):714-7. PubMed ID: 12362026
    [TBL] [Abstract][Full Text] [Related]  

  • 38. [Oligophrenia--selected syndromes XXI. Dyggve-Melchior-Clausen syndrome (DMC syndrome)].
    Dyggve HV; Melchior JC; Clausen J
    Ugeskr Laeger; 1973 Jan; 135(3):127. PubMed ID: 4265356
    [No Abstract]   [Full Text] [Related]  

  • 39. Dyggve-Melchior-Clausen syndrome with increased pipecolic acid in plasma and urine.
    Roesel RA; Carroll JE; Rizzo WB; van der Zalm T; Hahn DA
    J Inherit Metab Dis; 1991; 14(6):876-80. PubMed ID: 1779646
    [TBL] [Abstract][Full Text] [Related]  

  • 40. [Dyggve-Melchior-Clausen syndrome: description of 2 further cases].
    Galasso C; Fabbri F; Pagnotta G; Palusci A; Sanna ML; Serrao Arnone D; Scirè G
    Pediatr Med Chir; 1995; 17(6):573-6. PubMed ID: 8668596
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 10.