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23. The Dyggve-Melchior-Clausen syndrome. Spranger J; Maroteaux P; Der Kaloustian VM Radiology; 1975 Feb; 114(2):415-21. PubMed ID: 803318 [TBL] [Abstract][Full Text] [Related]
24. An extremely rare association of dyggve-melchior-clausen syndrome with mania: coincidence or comorbidity. Kar SK; Bansal S; Kumar D Indian J Psychol Med; 2015; 37(2):226-9. PubMed ID: 25969613 [TBL] [Abstract][Full Text] [Related]
25. A Novel Homozygous Nonsense Variant in the Bakar A; Shams S; Bibi N; Ullah A; Ahmad W; Jelani M; Muthaffar OY; Abdulkareem AA; Abujamel TS; Haque A; Naseer MI; Khan B Genes (Basel); 2023 Feb; 14(2):. PubMed ID: 36833437 [TBL] [Abstract][Full Text] [Related]
26. [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]
27. Evidence that Smith-McCort dysplasia and Dyggve-Melchior-Clausen dysplasia are allelic disorders that result from mutations in a gene on chromosome 18q12. Ehtesham N; Cantor RM; King LM; Reinker K; Powell BR; Shanske A; Unger S; Rimoin DL; Cohn DH Am J Hum Genet; 2002 Oct; 71(4):947-51. PubMed ID: 12161821 [TBL] [Abstract][Full Text] [Related]
28. [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]
29. 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]
30. A new locus for Seckel syndrome on chromosome 18p11.31-q11.2. Børglum AD; Balslev T; Haagerup A; Birkebaek N; Binderup H; Kruse TA; Hertz JM Eur J Hum Genet; 2001 Oct; 9(10):753-7. PubMed ID: 11781686 [TBL] [Abstract][Full Text] [Related]
31. New autosomal recessive syndrome of mental retardation, epilepsy, short stature, and skeletal dysplasia. Gurrieri F; Sammito V; Bellussi A; Neri G Am J Med Genet; 1992 Oct; 44(3):315-20. PubMed ID: 1488978 [No Abstract] [Full Text] [Related]
32. Dyggve-Melchiore-Clausen dysplasia (DMC): syndrome associated with a micropenis. Latrech H; Skiker I; Bentata Y; Alami Z; Mouhib Lav O; Oulali N; Benajiba N; Benmassoud S; El Jabri M; Gaouzi A; Gharbi MH; Chradibi A Pediatr Endocrinol Rev; 2013 Dec; 11(2):181-5. PubMed ID: 24575553 [TBL] [Abstract][Full Text] [Related]
39. Dyggve-Melchior-Clausen syndrome and Smith-McCort dysplasia: clinical and molecular findings in three families supporting genetic heterogeneity in Smith-McCort dysplasia. Neumann LM; El Ghouzzi V; Paupe V; Weber HP; Fastnacht E; Leenen A; Lyding S; Klusmann A; Mayatepek E; Pelz J; Cormier-Daire V Am J Med Genet A; 2006 Mar; 140(5):421-6. PubMed ID: 16470731 [TBL] [Abstract][Full Text] [Related]
40. 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] [Previous] [Next] [New Search]