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Journal Abstract Search

211 related items for PubMed ID: 3890548

  • 1. Syndrome of camptodactyly, ankyloses, facial anomalies, and pulmonary hypoplasia (Pena-Shokeir syndrome): obstetric and ultrasound aspects.
    Shenker L, Reed K, Anderson C, Hauck L, Spark R.
    Am J Obstet Gynecol; 1985 Jun 01; 152(3):303-7. PubMed ID: 3890548
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  • 2. The Pena-Shokeir syndrome: report of five cases and further delineation of the syndrome.
    Chen H, Blumberg B, Immken L, Lachman R, Rightmire D, Fowler M, Bachman R, Beemer FA.
    Am J Med Genet; 1983 Oct 01; 16(2):213-24. PubMed ID: 6650566
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  • 3. Fetal akinesia deformation sequence (Pena-Shokeir phenotype) associated with acquired intrauterine brain damage.
    Lavi E, Montone KT, Rorke LB, Kliman HJ.
    Neurology; 1991 Sep 01; 41(9):1467-8. PubMed ID: 1891100
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  • 5. Syndrome of camptodactyly, multiple ankyloses, facial anomalies and pulmonary hypoplasia--further delineation and evidence for autosomal recessive inheritance.
    Pena SD, Shokeir MH.
    Birth Defects Orig Artic Ser; 1976 Sep 01; 12(5):201-8. PubMed ID: 953225
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  • 7. Syndrome of camptodactyly, multiple ankyloses, facial anomalies, and pulmonary hypoplasia: a lethal condition.
    Pena SD, Shokeir MH.
    J Pediatr; 1974 Sep 01; 85(3):373-5. PubMed ID: 4431498
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  • 8. [Pena-Shokeir syndrome type I--combination of polyhydramnios and pulmonary hypoplasia in fetal akinesia].
    Deli T, Kovács T.
    Orv Hetil; 2010 Jun 13; 151(24):990-3. PubMed ID: 20519182
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  • 9. [Pena-Shokeir phenotype (fetal akinesia/hypokinesia sequence)].
    Dzinović A, Heljić S.
    Med Arh; 2006 Jun 13; 60(6):383-5. PubMed ID: 17297855
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  • 10. Sibs with the fetal akinesia sequence, fetal edema, and malformations: a new syndrome?
    Toriello HV, Bauserman SC, Higgins JV.
    Am J Med Genet; 1985 Jun 13; 21(2):271-7. PubMed ID: 4040328
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  • 11. Pulmonary hypoplasia, multiple ankyloses, and camptodactyly: one syndrome or some related forms?
    Lazjuk GI, Cherstvoy ED, Lurie IW, Nedzved MK.
    Helv Paediatr Acta; 1978 Apr 13; 33(1):73-9. PubMed ID: 669973
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  • 12. Analysis of Pena Shokeir phenotype.
    Hall JG.
    Am J Med Genet; 1986 Sep 13; 25(1):99-117. PubMed ID: 3541610
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  • 13. Prenatal ultrasound of regional akinesia with Pena-Shokier phenotype.
    Tongsong T, Chanprapaph P, Khunamornpong S.
    Prenat Diagn; 2000 May 13; 20(5):422-5. PubMed ID: 10820413
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  • 14. Syndromes of camptodactyly, multiple ankylosis, facial anomalies, and pulmonary hypoplasia.
    Elias S, Boelen L, Simpson JL.
    Birth Defects Orig Artic Ser; 1978 May 13; 14(6B):243-51. PubMed ID: 728565
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  • 15. Prenatal ultrasonographic features of the Pena-Shokeir I syndrome and the trisomy 18 syndrome.
    Muller LM, de Jong G.
    Am J Med Genet; 1986 Sep 13; 25(1):119-29. PubMed ID: 3541607
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  • 17. [Pena-Shokeir syndrome: report of a case with benign outcome].
    Romeo MG, Betta P, Rodonò A, Tina LG, Distefano G.
    Pediatr Med Chir; 1995 Sep 13; 17(1):73-5. PubMed ID: 7739933
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  • 18. The Pena-Shokeir syndrome: report of nine Dutch cases.
    Lindhout D, Hageman G, Beemer FA, Ippel PF, Breslau-Siderius L, Willemse J.
    Am J Med Genet; 1985 Aug 13; 21(4):655-68. PubMed ID: 3895932
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