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Journal Abstract Search

369 related items for PubMed ID: 6506057

  • 1.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 2. [Anesthetic management of a patient with Dyggve-Melchior-Clausen syndrome].
    Eguchi M, Kadota Y, Yoshida Y, Masuda M, Masuyama T, Kammura Y.
    Masui; 2001 Oct; 50(10):1116-7. PubMed ID: 11712346
    [Abstract] [Full Text] [Related]

  • 3.
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  • 4. 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
    [Abstract] [Full Text] [Related]

  • 5. [Cardiac symptoms in 2 patients with Seckel syndrome].
    Rappen U, von Brenndorff AI.
    Monatsschr Kinderheilkd; 1993 Jul; 141(7):584-6. PubMed ID: 8413337
    [Abstract] [Full Text] [Related]

  • 6. X-linked Dyggve-Melchior-Clausen syndrome.
    Yunis E, Fontalvo J, Quintero L.
    Clin Genet; 1980 Oct; 18(4):284-90. PubMed ID: 7192195
    [Abstract] [Full Text] [Related]

  • 7. Autosomal recessive mode of inheritance of a Coffin-Siris like syndrome.
    Bonioli E, Palmieri A, Bertola A, Bellini C.
    Genet Couns; 1995 Oct; 6(4):309-12. PubMed ID: 8775417
    [Abstract] [Full Text] [Related]

  • 8. [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
    [Abstract] [Full Text] [Related]

  • 9. A syndrome of mental retardation, short stature, hemolytic anemia, delayed puberty, and abnormal facial appearance: similarities to a report of aldolase A deficiency.
    Hurst JA, Baraitser M, Winter RM.
    Am J Med Genet; 1987 Dec; 28(4):965-70. PubMed ID: 3688035
    [Abstract] [Full Text] [Related]

  • 10. A new syndrome of dwarfism, brachydactyly, nail dysplasia, and mental retardation in sibs.
    Tonoki H, Kishino T, Niikawa N.
    Am J Med Genet; 1990 May; 36(1):89-93. PubMed ID: 2333912
    [Abstract] [Full Text] [Related]

  • 11. [Dyggve-Melchior-Clausen syndrome].
    Kondoh T, Matsumoto T.
    Ryoikibetsu Shokogun Shirizu; 2000 May; (30 Pt 5):175-6. PubMed ID: 11057185
    [No Abstract] [Full Text] [Related]

  • 12. Tau syndrome (thrombocytopenia and absent ulnar) with mental retardation and facial dysmorphy.
    Stoll C, Finck S, Janser B, Printz M, Lutz P.
    Genet Couns; 1992 May; 3(1):41-7. PubMed ID: 1590980
    [Abstract] [Full Text] [Related]

  • 13. Familial partial duplication (1)(p21p31).
    Hoechstetter L, Soukup S, Schorry EK.
    Am J Med Genet; 1995 Nov 20; 59(3):291-4. PubMed ID: 8599351
    [Abstract] [Full Text] [Related]

  • 14. [Dyggve-melchior-clausen's syndrome (author's transl)].
    Serradell Capdevila J, Pascual Navarro JC.
    An Esp Pediatr; 1977 Nov 20; 10(8-9):677-81. PubMed ID: 414643
    [Abstract] [Full Text] [Related]

  • 15. The Dubowitz syndrome--one more case.
    Chrzanowska KH, Krajewska-Walasek M.
    Klin Padiatr; 1987 Nov 20; 199(5):370-2. PubMed ID: 3316825
    [Abstract] [Full Text] [Related]

  • 16. A previously undescribed autosomal recessive multiple congenital anomalies/mental retardation (MCA/MR) syndrome with growth failure, lip/palate cleft(s), and urogenital anomalies.
    Malpuech G, Demeocq F, Palcoux JB, Vanlieferinghen P.
    Am J Med Genet; 1983 Dec 20; 16(4):475-80. PubMed ID: 6660246
    [Abstract] [Full Text] [Related]

  • 17. Short stature, mental retardation, eye anomalies, and cleft lip/palate.
    Richieri-Costa A, Guion-Almeida ML.
    Am J Med Genet; 1992 Feb 15; 42(4):449-52. PubMed ID: 1609826
    [Abstract] [Full Text] [Related]

  • 18. Aminopterin Syndrome Sine Aminopterin (ASSA) syndrome in two siblings: further delineation of the syndrome and review of the literature.
    Krajewska-Walasek M.
    Genet Couns; 1994 Feb 15; 5(4):345-55. PubMed ID: 7888136
    [Abstract] [Full Text] [Related]

  • 19. New syndromes of mental retardation.
    Thurmon TF, Santos CL.
    Birth Defects Orig Artic Ser; 1975 Feb 15; 11(2):264-8. PubMed ID: 1227531
    [Abstract] [Full Text] [Related]

  • 20. Genomic duplication in Dyggve Melchior Clausen syndrome, a novel mutation mechanism in an autosomal recessive disorder.
    Kinning E, Tufarelli C, Winship WS, Aldred MA, Trembath RC.
    J Med Genet; 2005 Dec 15; 42(12):e70. PubMed ID: 16326827
    [Abstract] [Full Text] [Related]

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