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22. Duplication 8p syndrome: studies in a family with a reciprocal translocation between chromosomes 8 and 12. Moreno Fuenmayor HM; Meilinger KL; Rucknagel DL; Mohrenweiser HL; Chu EH Am J Med Genet; 1980; 7(3):361-8. PubMed ID: 7468661 [TBL] [Abstract][Full Text] [Related]
23. [Partial trisomy of the long arm of chromosome 2 by malsegregation of a maternal translocation t(2;7)(q321;p22)]. Siffroi JP; Romani F; Viguié F; Lejeune C Ann Genet; 1984; 27(4):241-4. PubMed ID: 6335372 [TBL] [Abstract][Full Text] [Related]
24. [Partial monosomy and trisomy 5 p due to balanced translocation t (3,5) in the father (author's transl)]. Andrle M; Erlach A; Rett A Wien Klin Wochenschr; 1981 Jan; 93(1):16-9. PubMed ID: 7222705 [TBL] [Abstract][Full Text] [Related]
25. Partial trisomy 16q resulting from maternal translocation 11p/16q. Calva P; Frias S; Carnevale A; Reyes P Ann Genet; 1984; 27(2):122-5. PubMed ID: 6331790 [TBL] [Abstract][Full Text] [Related]
26. Partial trisomy 12p. A newborn child with karyotype 46,XY,der(11), t(11; 12) (q25; p11) mat. Case report and review. Ottolina de Bracamonte N; Velazco JQ; Hammond Figueroa FG Acta Cient Venez; 1982; 33(4):342-7. PubMed ID: 7186725 [No Abstract] [Full Text] [Related]
27. A case of partial trisomy 8p resulting from a maternal balanced translocation. Clark CE; Telfer MA; Cowell HR Am J Med Genet; 1980; 7(1):21-5. PubMed ID: 7211950 [No Abstract] [Full Text] [Related]
28. [Trisomy 10 p. Apropos of a case caused by a maternal translocation]. Stoll C; Willard D Pediatrie; 1980; 35(3):251-5. PubMed ID: 7393692 [No Abstract] [Full Text] [Related]
29. [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]
30. [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; 16(3):257-67. PubMed ID: 5683042 [No Abstract] [Full Text] [Related]
31. Partial trisomy of chromosome number 15 identified by trypsin-Giemsa banding. Crandall BF; Muller HM; Bass HN Am J Ment Defic; 1973 Mar; 77(5):571-8. PubMed ID: 4703990 [No Abstract] [Full Text] [Related]
32. [12 p trisomy. A new case (author's transl)]. Kubryk N; Prieur M; Borde M Ann Pediatr (Paris); 1980 Dec; 27(10):695-9. PubMed ID: 7212558 [No Abstract] [Full Text] [Related]
33. [Partial trisomy 9 (p 12--q ter), "de novo" in mosaic]. Ioan D; Ioan A; Bene M; Dumitriu L; Pană I; Pop T; Maximilian C Endocrinologie; 1984; 22(2):141-6. PubMed ID: 6740200 [No Abstract] [Full Text] [Related]
34. Aniridia and mental retardation with deletion of the short arm of chromosome 11. Kaiser-Kupfer MI; White BJ; Papadopoulos N Trans Am Ophthalmol Soc; 1981; 79():276-93. PubMed ID: 7342404 [No Abstract] [Full Text] [Related]
35. [Partial 11q trisomy due to missegregation of maternal t(11;22) (q23;q11.1) translocation (author's transl)]. Pangalos C; Couturier J; Bartsocas C; Theodorou S Nouv Presse Med; 1980 Nov; 9(41):3065-7. PubMed ID: 7443445 [TBL] [Abstract][Full Text] [Related]
36. [Rethoré syndrome (9p trisomy) with unusual karyotype: 46,XX,-9, + der 9p, t(9;9)mat]. Di Cesare D; Paludetto R; Casullo C; Pagano L; Stabile M; Sicolo A; Ventruto V Minerva Pediatr; 1980 Dec; 32(23):1349-52. PubMed ID: 7219376 [No Abstract] [Full Text] [Related]
37. Duplication 8q syndrome due to familial chromosome ins(10;8)(q21;q212q22). Bowen P; Fitzgerald PH; Gardner RJ; Biederman B; Veale AM Am J Med Genet; 1983 Apr; 14(4):635-46. PubMed ID: 6846399 [TBL] [Abstract][Full Text] [Related]
38. [Abnormalities syndrome in trisomy 9p]. Neuhäuser G Hippokrates; 1975 Nov; 46(4):504-5. PubMed ID: 1238381 [No Abstract] [Full Text] [Related]
39. Trisomy 6q25 leads to 6qter in two sisters resulting from maternal 6;11 translocation. Clark CE; Cowell HR; Telfer MA; Casey PA Am J Med Genet; 1980; 5(2):171-8. PubMed ID: 7395910 [TBL] [Abstract][Full Text] [Related]
40. [Reciprocal translocation between a chromosome number 21 (G1) and a chromosome of the group C(C6)]. Pfeiffer RA; Laermann J; Heidtmann HL Helv Paediatr Acta; 1967 Dec; 22(6):558-64. PubMed ID: 4232885 [No Abstract] [Full Text] [Related] [Previous] [Next] [New Search]