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Journal Abstract Search
143 related items for PubMed ID: 2494224
1. Bone and joint manifestations of Rieger's syndrome: a report of a family. Koshino T, Konno T, Ohzeki T. J Pediatr Orthop; 1989; 9(2):224-30. PubMed ID: 2494224 [Abstract] [Full Text] [Related]
2. [2 cases of Rieger's syndrome. Malformations of the anterior segment associated with facial bone abnormalities]. Levy D, Johner D, Guillaumat L. Bull Soc Ophtalmol Fr; 1973; 73(9-10):907-16. PubMed ID: 4214624 [No Abstract] [Full Text] [Related]
3. Morphology of the sella turcica in Axenfeld-Rieger syndrome with PITX2 mutation. Meyer-Marcotty P, Weisschuh N, Dressler P, Hartmann J, Stellzig-Eisenhauer A. J Oral Pathol Med; 2008 Sep; 37(8):504-10. PubMed ID: 18331556 [Abstract] [Full Text] [Related]
5. Rieger's syndrome: a case report. Prabhu NT, John R, Munshi AK. Quintessence Int; 1997 Nov; 28(11):749-52. PubMed ID: 9573866 [Abstract] [Full Text] [Related]
6. [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; 50(9):666-70. PubMed ID: 8373549 [Abstract] [Full Text] [Related]
8. [Rieger's syndrome in a 12 year old girl]. Ginter M, Krawczyński M. Klin Oczna; 1994 Apr; 96(10-11):347-50. PubMed ID: 7715155 [Abstract] [Full Text] [Related]
9. Craniofacial anomalies, abnormal hair, camptodactyly, and caudal appendage (Teebi-Shaltout syndrome): clinical and autopsy findings. Froster UG, Rehder H, Höhn W, Oberheuser F. Am J Med Genet; 1993 Oct 01; 47(5):717-22. PubMed ID: 8267003 [Abstract] [Full Text] [Related]
10. [Hypoplasia of the pulmonary artery in Rieger's Syndrome (author's transl)]. Schmidt-Redemann B, Vogt J. Klin Padiatr; 1976 Nov 01; 188(6):554-7. PubMed ID: 826736 [Abstract] [Full Text] [Related]
11. SHORT syndrome: a new case with probable autosomal dominant inheritance. Sorge G, Ruggieri M, Polizzi A, Scuderi A, Di Pietro M. Am J Med Genet; 1996 Jan 11; 61(2):178-81. PubMed ID: 8669449 [Abstract] [Full Text] [Related]
12. [Clinical observation on Rieger's syndrome (report of 4 cases) (author's transl)]. Deng HJ. Zhonghua Yan Ke Za Zhi; 1981 Nov 11; 17(6):359-61. PubMed ID: 6806034 [No Abstract] [Full Text] [Related]
13. Oto-palato-digital syndrome with features of type I and II in brothers. Horn D, Nitz I, Bollmann R. Genet Couns; 1995 Nov 11; 6(3):233-40. PubMed ID: 8588852 [Abstract] [Full Text] [Related]
14. Acro-renal-ocular syndrome: autosomal dominant thumb hypoplasia, renal ectopia, and eye defect. Halal F, Homsy M, Perreault G. Am J Med Genet; 1984 Apr 11; 17(4):753-62. PubMed ID: 6426304 [Abstract] [Full Text] [Related]
15. Rieger's anomaly associated with Marfan's syndrome. Grin TR, Nelson LB. Ann Ophthalmol; 1987 Oct 11; 19(10):380-1, 384. PubMed ID: 3688720 [Abstract] [Full Text] [Related]
16. Osseous malformations associated with chromosome abnormalities. Weiss L, Reynolds WA. Orthop Clin North Am; 1972 Nov 11; 3(3):713-32. PubMed ID: 4264453 [No Abstract] [Full Text] [Related]
17. Megalocornea associated with multiple skeletal anomalies: a new genetic syndrome? Frank Y, Ziprkowski M, Romano A, Stein R, Katznelson MB, Cohen B, Goodman RM. J Genet Hum; 1973 Jun 11; 21(2):67-72. PubMed ID: 4805907 [No Abstract] [Full Text] [Related]