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2. 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 [No Abstract] [Full Text] [Related]
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 [TBL] [Abstract][Full Text] [Related]
4. 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]
5. 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 [No Abstract] [Full Text] [Related]
6. 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; 152(3):303-7. PubMed ID: 3890548 [TBL] [Abstract][Full Text] [Related]
7. Syndrome of ankylosis, facial anomalies and pulmonary hypoplasia. Khan AA Med J Zambia; 1977; 11(2):53-5. PubMed ID: 878635 [TBL] [Abstract][Full Text] [Related]
8. 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]
10. 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]
11. 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]
12. Syndrome of camptodactyly, facial anomalies, and pulmonary hypoplasia. Williams J; Cohen D; Scolnik B; Zakut C J Pediatr; 1978 Jul; 93(1):151-2. PubMed ID: 650330 [No Abstract] [Full Text] [Related]
14. Anomalies in an infant with Nager acrofacial dysostosis. Krauss CM; Hassell LA; Gang DL Am J Med Genet; 1985 Aug; 21(4):761-4. PubMed ID: 4025401 [TBL] [Abstract][Full Text] [Related]
16. 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; 85(4):499-504. PubMed ID: 2314962 [TBL] [Abstract][Full Text] [Related]
17. 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; 58(4):348-52. PubMed ID: 8533844 [TBL] [Abstract][Full Text] [Related]
18. Ankylosis, facial anomalies, and pulmonary hypoplasia syndrome. Say B; Barber ND; Leichtman LG Am J Dis Child; 1979 Nov; 133(11):1196-7. PubMed ID: 507013 [No Abstract] [Full Text] [Related]
19. 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]
20. 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] [Next] [New Search]