These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
11. Arthrogryposis multiplex congenita, Pena-Shokeir phenotype, with gastroschisis and agenesis of the leg. Agapitos M; Georgiou-Theodoropoulou M; Koutselinis A; Papacharalambus N Pediatr Pathol; 1988; 8(4):409-13. PubMed ID: 2974953 [TBL] [Abstract][Full Text] [Related]
12. 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]
13. 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]
14. Arthrogryposis multiplex congenita: an autopsy case of a fatal form. Imamura M; Yamanaka N; Nakamura F; Oyanagi K Hum Pathol; 1981 Aug; 12(8):699-704. PubMed ID: 7286967 [TBL] [Abstract][Full Text] [Related]
19. [Clinical and ultrastructural study of a case of arthrogryposis]. Martin C; Vital C; Babin JP; Vallat JM; Heheunstre JP Arch Fr Pediatr; 1971 Apr; 28(4):445-6. PubMed ID: 5087589 [No Abstract] [Full Text] [Related]