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Journal Abstract Search

95 related items for PubMed ID: 878635

  • 1. Syndrome of ankylosis, facial anomalies and pulmonary hypoplasia.
    Khan AA.
    Med J Zambia; 1977; 11(2):53-5. PubMed ID: 878635
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  • 4. 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; 33(1):73-9. PubMed ID: 669973
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  • 6. Syndrome of ankylosis, facial anomalies, and pulmonary hypoplasia: a pathologic analysis of one infant.
    Dimmick JE, Berry K, MacLeod PM, Hardwick DF.
    Birth Defects Orig Artic Ser; 1977 Apr; 13(3D):133-7. PubMed ID: 922132
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  • 7. 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; 16(2):213-24. PubMed ID: 6650566
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  • 8. Syndrome of ankylosis, facial anomalies, and pulmonary hypoplasia.
    Punnett HH, Kistenmacher ML, Valdes-Dapena M, Ellison RT.
    J Pediatr; 1974 Sep; 85(3):375-7. PubMed ID: 4154411
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  • 9. Syndrome of camptodactyly, multiple ankyloses, facial anomalies, and pulmonary hypoplasia: a lethal condition.
    Pena SD, Shokeir MH.
    J Pediatr; 1974 Sep; 85(3):373-5. PubMed ID: 4431498
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  • 10. [Multiple pterygium syndrome. A case report (author's transl)].
    Zuccati Clauser G, Giovannucci Uzielli ML, Paoli A, Santoro S.
    Pathologica; 1981 Sep; 73(1023):23-9. PubMed ID: 6118848
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  • 12. Craniomicromelic syndrome: a newly recognized lethal condition with craniosynostosis, distinct facial anomalies, short limbs, and intrauterine growth retardation.
    Barr M, Heidelberger KP, Comstock CH.
    Am J Med Genet; 1995 Sep 25; 58(4):348-52. PubMed ID: 8533844
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  • 14. Acute respiratory distress in Pena-Shokeir syndrome.
    Boesen PV, French CE.
    Ear Nose Throat J; 2004 Nov 25; 83(11):772-3. PubMed ID: 15628635
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  • 15. Fryns syndrome survivors and neurologic outcome.
    Van Hove JL, Spiridigliozzi GA, Heinz R, McConkie-Rosell A, Iafolla AK, Kahler SG.
    Am J Med Genet; 1995 Nov 20; 59(3):334-40. PubMed ID: 8599357
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  • 16. [Fryns syndrome: report of the first case in the national literature].
    Rentería-Ibarra M, Frías-Márquez SG, Michel-Aceves RJ, Navarrete-Arellano M.
    Bol Med Hosp Infant Mex; 1993 Sep 20; 50(9):666-70. PubMed ID: 8373549
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  • 18. Fryns syndrome: a new variable multiple congenital anomaly (MCA) syndrome.
    Lubinsky M, Severn C, Rapoport JM.
    Am J Med Genet; 1983 Mar 20; 14(3):461-6. PubMed ID: 6859098
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  • 19. Variation in clinical and genitourinary lesions associated with pulmonary hypoplasia in Potter's syndrome--two autopsy reports.
    Jain M, Agarwal S, Mandal S.
    Indian J Pathol Microbiol; 2006 Jul 20; 49(3):416-8. PubMed ID: 17001905
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