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Journal Abstract Search
114 related items for PubMed ID: 8669446
1. Additional case of craniofacial and digital anomalies as reported by Harrod et al. Jurenka SB, Van Allen MI. Am J Med Genet; 1996 Jan 11; 61(2):168-70. PubMed ID: 8669446 [Abstract] [Full Text] [Related]
2. Megadolichosigmoid in a young male with Aarskog syndrome. Casteels M, Samain H, Penninckx F, Coremans G, Beirinckx J, Fryns JP. Genet Couns; 1994 Jan 11; 5(1):81-3. PubMed ID: 8031541 [No Abstract] [Full Text] [Related]
3. Kabuki make-up syndrome and hearing impairment. Say B, McCutcheon L, Todd C, Hough JV. Clin Dysmorphol; 1993 Jan 11; 2(1):68-70. PubMed ID: 8298741 [Abstract] [Full Text] [Related]
4. Smith-Fineman-Myers syndrome: report of a third case. Stephenson LD, Johnson JP. Am J Med Genet; 1985 Oct 11; 22(2):301-4. PubMed ID: 4050861 [Abstract] [Full Text] [Related]
6. Fragile X family with unusual digital and facial abnormalities, cleft lip and palate, and epilepsy. Loesch DZ, Hay DA, Sheffield LJ. Am J Med Genet; 1992 Nov 15; 44(5):543-50. PubMed ID: 1481805 [Abstract] [Full Text] [Related]
7. Microcephaly and digital anomalies: a newly recognized syndrome of recessively inherited mental retardation. Kelly TE, Kirson L, Wyatt J. Am J Med Genet; 1993 Feb 01; 45(3):353-5. PubMed ID: 8434622 [Abstract] [Full Text] [Related]
8. Oto-palato-digital syndrome with features of type I and II in brothers. Horn D, Nitz I, Bollmann R. Genet Couns; 1995 Feb 01; 6(3):233-40. PubMed ID: 8588852 [Abstract] [Full Text] [Related]
20. The craniodigital syndrome of Scott: report of a second family. Lorenz P, Hinkel GK, Hoffmann C, Rupprecht E. Am J Med Genet; 1990 Oct 01; 37(2):224-6. PubMed ID: 2174209 [Abstract] [Full Text] [Related] Page: [Next] [New Search]