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22. [Mental retardation and sexual development in chromosomal syndrome (author's transl)]. Balestrazzi P; Bernasconi S; Medioli FC; Corrini L; Villani G Ateneo Parmense Acta Biomed; 1980; 51(1):45-51. PubMed ID: 7470180 [TBL] [Abstract][Full Text] [Related]
23. The 18p- syndrome. Report of five cases. Zumel RM; Darnaude MT; Delicado A; Diaz de Bustamante A; de Torres ML; López-Pájares I Ann Genet; 1989; 32(3):160-3. PubMed ID: 2817777 [TBL] [Abstract][Full Text] [Related]
25. Cytogenetics in mentally defective children with anomalies: a controlled study. Summitt RL J Pediatr; 1969 Jan; 74(1):58-66. PubMed ID: 5782825 [No Abstract] [Full Text] [Related]
26. Skeletal changes in the Cornelia de Lange syndrome. Lee FA; Kenny FM Am J Roentgenol Radium Ther Nucl Med; 1967 May; 100(1):27-39. PubMed ID: 6023899 [No Abstract] [Full Text] [Related]
27. Trisomy 9p with i(9p) and t(9q18p). Herva R; Koivisto M Hum Genet; 1979 Sep; 50(3):237-40. PubMed ID: 489006 [TBL] [Abstract][Full Text] [Related]
28. [Idiopathic multicentric osteolysis with craniodysplasis and mental retardation: a new syndrome? (author's transl)]. Mathias K; Ludwig U Rofo; 1977 Sep; 127(3):255-61. PubMed ID: 143430 [TBL] [Abstract][Full Text] [Related]
29. Cranial hemihypertrophy with ipsilateral naevoid streaks, intellectual handicap and epilepsy: a report of two cases. McMullin GP; Super M; Clarke MA Clin Genet; 1993 Nov; 44(5):249-53. PubMed ID: 8313622 [TBL] [Abstract][Full Text] [Related]
30. [Rare case of mosaicism for chromosome 18, karyotype: 46, XX, del(18) (p11)/46, XX, i(18q)]. Badalian LO; Mutovin GR; Malygina NA; Petrukhin AS Genetika; 1983 Nov; 19(11):1912-5. PubMed ID: 6686175 [TBL] [Abstract][Full Text] [Related]
31. [Morphological manifestations and principles of the differential diagnosis of chromosome diseases caused by changes in the autosome system]. Laziuk GI Arkh Patol; 1975; 37(10):3-11. PubMed ID: 131533 [TBL] [Abstract][Full Text] [Related]
32. Absence of IgA and growth hormone deficiency associated with short arm deletion of chromosome 18. Leisti J; Leisti S; Perheentupa J; Savilahti E; Aula P Arch Dis Child; 1973 Apr; 48(4):320-2. PubMed ID: 4705937 [No Abstract] [Full Text] [Related]
33. Evaluation of the child with idiopathic mental retardation. Schaefer GB; Bodensteiner JB Pediatr Clin North Am; 1992 Aug; 39(4):929-43. PubMed ID: 1635812 [TBL] [Abstract][Full Text] [Related]
35. [The deletion of the short arm of chromosome 18 (18p- syndrome), apropos of a new observation]. Gilgenkrantz S; Marchal C; Neimann N Ann Genet; 1968 Mar; 11(1):17-21. PubMed ID: 5301751 [No Abstract] [Full Text] [Related]
36. [Changes in the central nervous system in chromosomal diseases caused by autosomal abberrations]. Nedz'ved' MK; Laziuk GI; Lur'e IV Arkh Patol; 1974; 36(7):9-18. PubMed ID: 4281296 [No Abstract] [Full Text] [Related]
37. Cytogenetic abnormalities including the marker X chromosome in patients with severe mental retardation. Venter PA; Op't Hof J S Afr Med J; 1982 Dec; 62(25):947-50. PubMed ID: 6959296 [TBL] [Abstract][Full Text] [Related]
38. Human chromosome abnormalities as related to physical and mental dysfunction. Heller JH J Hered; 1969; 60(5):239-48. PubMed ID: 4244249 [No Abstract] [Full Text] [Related]