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Journal Abstract Search

317 related items for PubMed ID: 8862620

  • 1. A new Seckel-like syndrome of primordial dwarfism.
    Buebel MS, Salinas CF, Pai GS, Macpherson RI, Greer MK, Perez-Comas A.
    Am J Med Genet; 1996 Aug 23; 64(3):447-52. PubMed ID: 8862620
    [Abstract] [Full Text] [Related]

  • 2. [Intra uterine major dwarfism with dysmorphia and severe encephalopathy. Bird head dwarfism (Virchow-Seckel type)].
    Toudic L, Roche J, Alix D, Le Bars C, Dantoine G, Castel Y.
    Ann Pediatr (Paris); 1977 Oct 23; 24(10):653-6. PubMed ID: 16211901
    [No Abstract] [Full Text] [Related]

  • 3. A case of Seckel syndrome with Tetralogy of Fallot.
    Can E, Bulbul A, Uslu S, Demirin H, Comert S, Bolat F, Nuhoglu A.
    Genet Couns; 2010 Oct 23; 21(1):49-51. PubMed ID: 20420029
    [Abstract] [Full Text] [Related]

  • 4. [Differential diagnostic considerations in microcephalic dwarfism].
    Kraft CN, Diedrich O, Wagner U, Schmitt O.
    Z Orthop Ihre Grenzgeb; 2000 Oct 23; 138(2):126-30. PubMed ID: 10820877
    [Abstract] [Full Text] [Related]

  • 5. Not a new Seckel-like syndrome but ear-patella-short stature syndrome.
    Teebi AS, Gorlin RJ.
    Am J Med Genet; 1997 Jun 27; 70(4):454. PubMed ID: 9182792
    [No Abstract] [Full Text] [Related]

  • 6. Pigmentary changes and atopic dermatitis in a patient with Seckel syndrome.
    Brackeen A, Babb-Tarbox M, Smith J.
    Pediatr Dermatol; 2007 Jun 27; 24(1):53-6. PubMed ID: 17300651
    [Abstract] [Full Text] [Related]

  • 7. [Cardiac symptoms in 2 patients with Seckel syndrome].
    Rappen U, von Brenndorff AI.
    Monatsschr Kinderheilkd; 1993 Jul 27; 141(7):584-6. PubMed ID: 8413337
    [Abstract] [Full Text] [Related]

  • 8. Dental manifestations associated with Seckel syndrome type II: a case report.
    Regen A, Nelson LP, Woo SB.
    Pediatr Dent; 2010 Jul 27; 32(5):445-50. PubMed ID: 21070714
    [Abstract] [Full Text] [Related]

  • 9. Bird-headed dwarf of Seckel.
    Harsha Vardhan BG, Muthu MS, Saraswathi K, Koteeswaran D.
    J Indian Soc Pedod Prev Dent; 2007 Jul 27; 25 Suppl():S8-9. PubMed ID: 17921644
    [Abstract] [Full Text] [Related]

  • 10. 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 27; 15(4):338-41. PubMed ID: 15787928
    [Abstract] [Full Text] [Related]

  • 11. [Intrauterine dwarfism and dysmorfic features. A case of Russel-Silver syndrome].
    Peinado Garrido A, Borja Pérez C, Narbona López E, Contreras Chova F, Jerez Calero A, Miras Baldó M.
    An Esp Pediatr; 2001 Jun 27; 54(6):588-90. PubMed ID: 11412408
    [Abstract] [Full Text] [Related]

  • 12. [Camptomelic dwarfism].
    Ladreyt JP.
    Pediatrie; 1972 Jun 27; 27(5):567-8. PubMed ID: 5080135
    [No Abstract] [Full Text] [Related]

  • 13. Clinical and genetic heterogeneity of Seckel syndrome.
    Faivre L, Le Merrer M, Lyonnet S, Plauchu H, Dagoneau N, Campos-Xavier AB, Attia-Sobol J, Verloes A, Munnich A, Cormier-Daire V.
    Am J Med Genet; 2002 Nov 01; 112(4):379-83. PubMed ID: 12376940
    [Abstract] [Full Text] [Related]

  • 14. [Congenital dwarfisms with dysmorphism. 2. Bird-head congenital dwarfism (Virchow-Seckel type)].
    Anoussakis C, Liakakos D, Zervos N, Karpathios T.
    Pediatrie; 1974 Nov 01; 29(3):261-7. PubMed ID: 4438033
    [No Abstract] [Full Text] [Related]

  • 15. 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 01; 12(1):23-35. PubMed ID: 7201238
    [Abstract] [Full Text] [Related]

  • 16. T-cell clonality and myelodysplasia without chromosomal fragility in a patient with features of Seckel syndrome.
    Chanan-Khan A, Holkova B, Perle MA, Reich E, Wu CD, Inghirami G, Takeshita K.
    Haematologica; 2003 May 01; 88(5):ECR14. PubMed ID: 12745283
    [Abstract] [Full Text] [Related]

  • 17. Seckel syndrome with polyarteritis nodosa.
    Kutlu R, Alkan A, Kutlu O, Yakinci C.
    Indian Pediatr; 2004 Nov 01; 41(11):1158-61. PubMed ID: 15591669
    [Abstract] [Full Text] [Related]

  • 18. Central nervous system anomalies in Seckel syndrome: report of a new family and review of the literature.
    Shanske A, Caride DG, Menasse-Palmer L, Bogdanow A, Marion RW.
    Am J Med Genet; 1997 May 16; 70(2):155-8. PubMed ID: 9128935
    [Abstract] [Full Text] [Related]

  • 19. Seckel syndrome in a family with three affected children and hematological manifestations associated with chromosome instability.
    Syrrou M, Georgiou I, Paschopoulos M, Lolis D.
    Genet Couns; 1995 May 16; 6(1):37-41. PubMed ID: 7794560
    [Abstract] [Full Text] [Related]

  • 20. Interstitial deletion 2q33.3-q34 in a boy with a phenotype resembling the Seckel syndrome.
    Courtens W, Speleman F, Messiaen L, Bormans J, Van Roy N, Vamos E.
    Am J Med Genet; 1997 Sep 05; 71(4):479-85. PubMed ID: 9286460
    [Abstract] [Full Text] [Related]

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