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Journal Abstract Search

267 related items for PubMed ID: 953225

  • 1. 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; 12(5):201-8. PubMed ID: 953225
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  • 2. A syndrome of ankylosis, facial anomalies and pulmonary hypoplasia secondary to fetal neuromuscular dysfunction.
    Mease AD, Yeatman GW, Pettett G, Merenstein GB.
    Birth Defects Orig Artic Ser; 1976; 12(5):193-200. PubMed ID: 953224
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  • 3. 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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  • 9. Fryns syndrome.
    Stratton RF, Young RS, Heiman HS, Carter JM.
    Am J Med Genet; 1993 Mar 01; 45(5):562-4. PubMed ID: 8456824
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  • 12. Fryns syndrome: an autosomal recessive disorder associated with craniofacial anomalies, diaphragmatic hernia, and distal digital hypoplasia.
    Cunniff C, Jones KL, Saal HM, Stern HJ.
    Pediatrics; 1990 Apr 01; 85(4):499-504. PubMed ID: 2314962
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  • 16. Acute respiratory distress in Pena-Shokeir syndrome.
    Boesen PV, French CE.
    Ear Nose Throat J; 2004 Nov 01; 83(11):772-3. PubMed ID: 15628635
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  • 17. Autosomal recessive intestinal lymphangiectasia and lymphedema, with facial anomalies and mental retardation.
    Hennekam RC, Geerdink RA, Hamel BC, Hennekam FA, Kraus P, Rammeloo JA, Tillemans AA.
    Am J Med Genet; 1989 Dec 01; 34(4):593-600. PubMed ID: 2624276
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  • 20. Syndrome of ankylosis, facial anomalies, and pulmonary hypoplasia.
    Punnett HH, Kistenmacher ML, Valdes-Dapena M, Ellison RT.
    J Pediatr; 1974 Sep 01; 85(3):375-7. PubMed ID: 4154411
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