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Journal Abstract Search
192 related items for PubMed ID: 2729348
1. Acrocallosal syndrome in a girl born to consanguineous parents. Salgado LJ, Ali CA, Castilla EE. Am J Med Genet; 1989 Mar; 32(3):298-300. PubMed ID: 2729348 [Abstract] [Full Text] [Related]
2. Hypogenitalism in the acrocallosal syndrome. Temtamy SA, Meguid NA. Am J Med Genet; 1989 Mar; 32(3):301-5. PubMed ID: 2658583 [Abstract] [Full Text] [Related]
3. Hallux duplication, postaxial polydactyly, absence of the corpus callosum, severe mental retardation, and additional anomalies in two unrelated patients: a new syndrome. Schinzel A, Schmid W. Am J Med Genet; 1980 Mar; 6(3):241-9. PubMed ID: 7424976 [Abstract] [Full Text] [Related]
4. Peters'-Plus syndrome with agenesis of the corpus callosum: report of a case and confirmation of autosomal recessive inheritance. Camera G, Centa A, Pozzolo S, Camera A. Clin Dysmorphol; 1993 Oct; 2(4):317-21. PubMed ID: 8305962 [Abstract] [Full Text] [Related]
6. Greig cephalopolysyndactyly syndrome with dysgenesis of the corpus callosum in a Bedouin family. Marafie MJ, Temtamy SA, Rajaram U, al-Awadi SA, el-Badramany MH, Farag TI. Am J Med Genet; 1996 Dec 18; 66(3):261-4. PubMed ID: 8985483 [Abstract] [Full Text] [Related]
8. Acrocallosal syndrome in a child with de novo inverted tandem duplication of 12p11.2-p13.3. Pfeiffer RA, Legat G, Trautmann U. Ann Genet; 1992 Dec 18; 35(1):41-6. PubMed ID: 1610119 [Abstract] [Full Text] [Related]
9. [Familial agenesis of the corpus callosum: a new form]. Castro-Gago M, Rodriguez-Nuñez A, Eiris J, Peña J, Tojo R, Novo-Rodriguez I. Arch Fr Pediatr; 1993 Apr 18; 50(4):327-30. PubMed ID: 8379821 [Abstract] [Full Text] [Related]
10. The acrocallosal syndrome. Nelson MM, Thomson AJ. Am J Med Genet; 1982 Jun 18; 12(2):195-9. PubMed ID: 7102724 [Abstract] [Full Text] [Related]
11. Opitz trigonocephaly syndrome. Haaf T, Hofmann R, Schmid M. Am J Med Genet; 1991 Sep 15; 40(4):444-6. PubMed ID: 1746609 [Abstract] [Full Text] [Related]
13. Acrocallosal syndrome: report of a Brazilian girl. Guion-Almeida ML, Richieri-Costa A. Am J Med Genet; 1992 Aug 01; 43(6):938-41. PubMed ID: 1415343 [Abstract] [Full Text] [Related]
14. [The acrocallosal syndrome. Report of an additional case]. Wendisch J, Lorenz P, Kabus M, Rupprecht E, Walther S. Kinderarztl Prax; 1990 Jun 01; 58(6):315-21. PubMed ID: 2166860 [Abstract] [Full Text] [Related]
15. Acrocallosal syndrome in an Algerian boy born to consanguineous parents: review of the literature and further delineation of the syndrome. Courtens W, Vamos E, Christophe C, Schinzel A. Am J Med Genet; 1997 Mar 03; 69(1):17-22. PubMed ID: 9066878 [Abstract] [Full Text] [Related]
16. Acrocallosal syndrome in two African brothers born to consanguineous parents. Christianson AL, Venter PA, Du Toit JL, Shipalana N, Gericke GS. Am J Med Genet; 1994 Jun 01; 51(2):98-101. PubMed ID: 8092201 [Abstract] [Full Text] [Related]
17. A previously undescribed autosomal recessive multiple congenital anomalies/mental retardation (MCA/MR) syndrome with fronto-nasal dysostosis, cleft lip/palate, limb hypoplasia, and postaxial poly-syndactyly: acro-fronto-facio-nasal dysostosis syndrome. Richieri-Costa A, Colletto GM, Gollop TR, Masiero D. Am J Med Genet; 1985 Apr 01; 20(4):631-8. PubMed ID: 2986457 [Abstract] [Full Text] [Related]
19. Jancar syndrome: mental retardation, spasticity, and distal transverse limbs defects. Zlotogora J, Glick B. Am J Med Genet; 1993 Aug 01; 47(1):89-90. PubMed ID: 8368260 [Abstract] [Full Text] [Related]
20. Callosal defect, microcephaly, severe mental retardation, and other anomalies in three sibs. da-Silva EO. Am J Med Genet; 1988 Apr 01; 29(4):837-43. PubMed ID: 3400727 [Abstract] [Full Text] [Related] Page: [Next] [New Search]