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5. 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; 13(3D):133-7. PubMed ID: 922132 [No Abstract] [Full Text] [Related]
6. 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 [TBL] [Abstract][Full Text] [Related]
7. 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 [No Abstract] [Full Text] [Related]
8. New hereditary malformation syndrome of unusual facial appearance, skeletal deformities, and musculoskeletal and sensory defects. Middleton LT; Anastasiades V; Panayidou K; Georghiou D; Kalli E; Gabriel G; Myrianthopoulos NC Am J Med Genet; 1992 Dec; 44(6):757-61. PubMed ID: 1481843 [TBL] [Abstract][Full Text] [Related]
9. Syndrome of mental retardation, facial anomalies, hypopituitarism, and distal arthrogryposis in sibs. Chitayat D; Hall JG; Couch RM; Phang MS; Baldwin VJ Am J Med Genet; 1990 Sep; 37(1):65-70. PubMed ID: 2240046 [TBL] [Abstract][Full Text] [Related]
10. 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 [TBL] [Abstract][Full Text] [Related]
15. The heterogeneity of the Pena-Shokeir syndrome. Hageman G; Willemse J; van Ketel BA; Barth PG; Lindhout D Neuropediatrics; 1987 Feb; 18(1):45-50. PubMed ID: 3561707 [TBL] [Abstract][Full Text] [Related]
16. Fryns syndrome without diaphragmatic hernia? Willems PJ; Keersmaekers GH; Dom KE; Colpaert C; Schatteman E; Vergote IB; Dumon JE Am J Med Genet; 1991 Nov; 41(2):255-7. PubMed ID: 1785645 [TBL] [Abstract][Full Text] [Related]
17. Two cases of fetal akinesia/hypokinesia sequence. Itoh K; Yokoyama N; Ishihara A; Kawai S; Takada S; Nishino M; Lee Y; Negishi H; Itoh H Pediatr Pathol; 1991; 11(3):467-77. PubMed ID: 1866365 [TBL] [Abstract][Full Text] [Related]
18. Fryns syndrome. Stratton RF; Young RS; Heiman HS; Carter JM Am J Med Genet; 1993 Mar; 45(5):562-4. PubMed ID: 8456824 [TBL] [Abstract][Full Text] [Related]
19. The adducted thumbs syndrome. An autosomal recessive disease with arthrogryposis, dysmyelination, craniostenosis, and cleft palate. Christian JC; Andrews PA; Conneally PM; Muller J Clin Genet; 1971; 2(2):95-103. PubMed ID: 5116596 [No Abstract] [Full Text] [Related]
20. Pathologic features in two siblings with the Pena-Shokeir I syndrome. Bisceglia M; Zelante L; Bosman C; Cera R; Dallapiccola B Eur J Pediatr; 1987 May; 146(3):283-7. PubMed ID: 3595647 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]