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Journal Abstract Search


153 related items for PubMed ID: 8985485

  • 21. Neurologic aspects of microcephalic osteodysplastic primordial dwarfism type II.
    Galasso C, Lo-Castro A, Lalli C, Cerminara C, Curatolo P.
    Pediatr Neurol; 2008 Jun; 38(6):435-8. PubMed ID: 18486828
    [Abstract] [Full Text] [Related]

  • 22. [Type II primordial microcephalic dwarfism. Report of a patient with completed growth].
    Théau D, Maroteaux P.
    Ann Pediatr (Paris); 1993 May; 40(5):323-8. PubMed ID: 8346886
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  • 25. Roentgenographic manifestations of the Prader-Willi syndrome.
    Pearson KD, Steinbach HL, Bier DM.
    Radiology; 1971 Aug; 100(2):369-77. PubMed ID: 5147402
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  • 26. Microcephalic osteodysplastic primordial dwarfism type II.
    al Gazali LI, Hamada M, Lytle W.
    Clin Dysmorphol; 1995 Jul; 4(3):234-8. PubMed ID: 7551160
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  • 27. Studies of microcephalic primordial dwarfism II: the osteodysplastic type II of primordial dwarfism.
    Majewski F, Ranke M, Schinzel A.
    Am J Med Genet; 1982 May; 12(1):23-35. PubMed ID: 7201238
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  • 28. Bone structure in two adult subjects with impaired minor spliceosome function resulting from RNU4ATAC mutations causing microcephalic osteodysplastic primordial dwarfism type 1 (MOPD1).
    Krøigård AB, Frost M, Larsen MJ, Ousager LB, Frederiksen AL.
    Bone; 2016 Nov; 92():145-149. PubMed ID: 27591150
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  • 31. Early prenatal diagnosis of polycystic pancreas with narrow thorax and short limb dwarfism.
    Bronstein M, Reichler A, Borochowitz Z, Bejar J, Drugan A.
    Am J Med Genet; 1994 Jan 01; 49(1):6-9. PubMed ID: 8172252
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  • 32. Familial pituitary dwarfism associated with an abnormal sella turcica.
    Ferrier PE, Stone EF.
    Pediatrics; 1969 May 01; 43(5):858-65. PubMed ID: 4305958
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  • 33. [Differential diagnostic considerations in microcephalic dwarfism].
    Kraft CN, Diedrich O, Wagner U, Schmitt O.
    Z Orthop Ihre Grenzgeb; 2000 May 01; 138(2):126-30. PubMed ID: 10820877
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  • 34. Microcephalic osteodysplastic primordial dwarfism, type II. Report of a case with characteristic skeletal features.
    Herman TE, Mendelsohn NJ, Dowton SB, McAlister WH.
    Pediatr Radiol; 1991 May 01; 21(8):602-4. PubMed ID: 1815189
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  • 35. "Ocular moyamoya" syndrome in a patient with features of microcephalic osteodysplastic primordial dwarfism type II.
    Bang GM, Kirmani S, Patton A, Pulido JS, Brodsky MC.
    J AAPOS; 2013 Feb 01; 17(1):100-2. PubMed ID: 23337351
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  • 36. Perinatal findings of Seckel syndrome: a case report of a fetus showing primordial dwarfism and severe microcephaly.
    Takikawa KM, Kikuchi A, Yokoyama A, Ono K, Iwasawa Y, Sunagawa S, Takagi K, Kawame H, Nakamura T.
    Fetal Diagn Ther; 2008 Feb 01; 24(4):405-8. PubMed ID: 18984961
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  • 37. Osteodysplastic primordial dwarfism: report of a further patient with manifestations similar to those seen in patients with types I and III.
    Winter RM, Wigglesworth J, Harding BN.
    Am J Med Genet; 1985 Jul 01; 21(3):569-74. PubMed ID: 4025388
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  • 38. Anesthesia for cleft lip surgery in a child with Seckel syndrome--a case report.
    Rajamani A, Kamat V, Murthy J, Hussain SA.
    Paediatr Anaesth; 2005 Apr 01; 15(4):338-41. PubMed ID: 15787928
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  • 39. [A new (brachymelic) type of primordial dwarfism (author's transl)].
    Majewski F, Spranger J.
    Monatsschr Kinderheilkd (1902); 1976 Jun 01; 124(6):499-503. PubMed ID: 934161
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  • 40. Majewski dwarfism type II: an atypical neuroradiological presentation with a novel variant in the PCNT gene.
    Alrajhi H, Alallah J, Shawli A, Alghamdi K, Hakami F.
    BMJ Case Rep; 2019 May 30; 12(5):. PubMed ID: 31151966
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