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Journal Abstract Search
136 related items for PubMed ID: 1233411
21. [Radiologic aspects of trisomy 17-18. Edward's syndrome]. Lurà A, Pistocchi GF, Dallapiccola B, Rovere V, Osti L. Nunt Radiol; 1967; 33():Suppl:163-87. PubMed ID: 5617435 [No Abstract] [Full Text] [Related]
22. Trisomy 4p: five new observations and overview. Dallapiccola B, Mastroiacovo PP, Montali E, Sommer A. Clin Genet; 1977 Dec; 12(6):344-56. PubMed ID: 563312 [Abstract] [Full Text] [Related]
23. Partial duplication of the long arm of chromosome 4. Fryns JP, van den Berghe H. Ann Genet; 1980 Dec; 23(1):52-3. PubMed ID: 6965843 [Abstract] [Full Text] [Related]
24. [Trisomy syndrome of the end section of the long arm of chromosome 4]. Stoll C, Roth MP, Dott B, Lutz P. Ann Pediatr (Paris); 1985 Jun; 32(6):527-30. PubMed ID: 4026150 [No Abstract] [Full Text] [Related]
25. [Trisomy 4p. Mirror duplication of the short arm of chromosome 4 de novo]. Boyer JP, Andrieux L, Noel L, Mottet J. Neuropsychiatr Enfance Adolesc; 1983 Jul; 31(7):319-21. PubMed ID: 6621831 [No Abstract] [Full Text] [Related]
26. COFS syndrome with familial 1;16 translocation. Temtamy SA, Meguid NA, Mahmoud A, Afifi HH, Gerzawy A, Zaki MS. Clin Genet; 1996 Oct; 50(4):240-3. PubMed ID: 9001808 [Abstract] [Full Text] [Related]
27. Pattern of malformations in the axial skeleton in human trisomy 18 fetuses. Kjaer I, Keeling JW, Hansen BF. Am J Med Genet; 1996 Nov 11; 65(4):332-6. PubMed ID: 8923945 [Abstract] [Full Text] [Related]
28. [Changes in the central nervous system in chromosomal diseases caused by autosomal abberrations]. Nedz'ved' MK, Laziuk GI, Lur'e IV. Arkh Patol; 1974 Nov 11; 36(7):9-18. PubMed ID: 4281296 [No Abstract] [Full Text] [Related]
29. Trisomy 4p in a family with A t(4;15). Hustinx WJ, Gabreëls JM, Kirkels VG, Korten JJ, Scheres JM, Joosten EM, Rutten FJ. Ann Genet; 1975 Mar 11; 18(1):13-9. PubMed ID: 1080034 [Abstract] [Full Text] [Related]
30. [Morphological manifestations and principles of the differential diagnosis of chromosome diseases caused by changes in the autosome system]. Laziuk GI. Arkh Patol; 1975 Mar 11; 37(10):3-11. PubMed ID: 131533 [Abstract] [Full Text] [Related]
32. [Mental retardation in the crying cat syndrome. Comparison of the intellectual level in the partial deletion of the short arm of chromosome 5 with trisomy 21 and deletions of chromosome 18. Apropos of 118 cases taken from the literature]. Moor L. Rev Neuropsychiatr Infant; 1968 Mar 11; 16(3):257-67. PubMed ID: 5683042 [No Abstract] [Full Text] [Related]
33. [Trisomy 5p: a report of 2 cases]. Alvarez-Coca J, García-Alix A, Delicado A, González M, Escribá R, López Pajares I, Morena V, Peralta A. An Esp Pediatr; 1985 Mar 31; 22(4):288-92. PubMed ID: 4003955 [Abstract] [Full Text] [Related]
34. Trisomy 9p in a patient with a de novo 9/15 translocation. Jacobsen P, Hobolth N, Mikkelsen M. Clin Genet; 1975 Apr 31; 7(4):317-24. PubMed ID: 1126053 [Abstract] [Full Text] [Related]
39. Chromosome disorders associated with mental retardation. Brewster TG, Gerald PS. Pediatr Ann; 1978 Feb 31; 7(2):82-9. PubMed ID: 146845 [No Abstract] [Full Text] [Related]
40. [Edwards' trisomy (E syndrome). Report of a case]. Ceron Esquivel A, Alvarado Villaseñor A, Tellez Hurtado R. Prensa Med Mex; 1970 Feb 31; 35(9):356-8. PubMed ID: 5518415 [No Abstract] [Full Text] [Related] Page: [Previous] [Next] [New Search]