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2. Inherited translocations in two families (t(14q+;10q-) and t(13q-;21q+)). Talvik T; Mikelsaar AV; Mikelsaar R; Käosaar M; Tüür S Humangenetik; 1973 Sep; 19(3):215-26. PubMed ID: 4763926 [No Abstract] [Full Text] [Related]
3. An inherited small extra chromosome: a mother with 46,XX,t(17;22)(pl;ql) and a son with 47,XY,+der(22)mat. Borgaonkar DS; McKusick VA; Farber PA J Med Genet; 1973 Dec; 10(4):379-84. PubMed ID: 4129973 [TBL] [Abstract][Full Text] [Related]
4. Deletion of the long arms of chromosome 18 (46,XX,18q-) associated with absence of IgA and hypothyroidism in an adult. Faed MJ; Whyte R; Paterson CR; McCathie M; Robertson J J Med Genet; 1972 Mar; 9(1):102-5. PubMed ID: 4112566 [No Abstract] [Full Text] [Related]
5. [Observation of 7 cases of rare autosomal pathology. Trisomy 9p; monosomy 18q; ring 21; trisomy 6p; trisomy 2q 1-21 translocation]. Fioretti G; Pagano L; Renda S; Festa B; Rinaldi A; Celona A; Casullo C; Stabile M; Cavaliere ML; Ventruto V Minerva Pediatr; 1980 Jun; 32(12):807-14. PubMed ID: 7464734 [No Abstract] [Full Text] [Related]
7. Bisatellited extra small metacentric chromosome in newborns. Friedrich U; Nielsen J Clin Genet; 1974; 6(1):23-31. PubMed ID: 4426127 [No Abstract] [Full Text] [Related]
8. Three families with abnormal, inherited chromosomes: 2q+mat, t(Cp+; 13q-)mat and t(3?-;5q+)pat. Neu RL; Gardner LI Ann Genet; 1972 Mar; 15(1):19-23. PubMed ID: 4402505 [No Abstract] [Full Text] [Related]
9. Developmental and other pathologic changes in syndromes caused by chromosome abnormalities. Gilbert EF; Opitz JM Perspect Pediatr Pathol; 1982; 7():1-63. PubMed ID: 6214761 [No Abstract] [Full Text] [Related]
10. Dicentric chromosome due to an unusual fusion. Subrt I; Blehová B; Táborský O Humangenetik; 1971; 12(2):136-41. PubMed ID: 5568732 [No Abstract] [Full Text] [Related]
11. [Trisomy 10p as a result of familial 10/22 translocation]. Zergollern L; Begovic D; Muzinić D Acta Med Iugosl; 1980; 34(2):113-22. PubMed ID: 7405617 [No Abstract] [Full Text] [Related]
14. A balanced 13-18 translocation [46,XY,t(13q-;18q+)] in the father of an infant with multiple anomalies. McGilvray E; Kajii T; Freund M; Bamatter F; Klein D Humangenetik; 1971; 12(4):316-22. PubMed ID: 5564360 [No Abstract] [Full Text] [Related]
15. Tetrasomy 18p: a distinctive syndrome. Rivera H; Möller M; Hernández A; Enríquez-Guerra MA; Arreola R; Cantú JM Ann Genet; 1984; 27(3):187-9. PubMed ID: 6334486 [TBL] [Abstract][Full Text] [Related]
16. [2 cases of partial trisomy 10p due to a paternal translocation t(10p;18)(p13;q23)]. Morić-Petrović S; Laća Z; Krajgher A; Milośevic J Ann Genet; 1976 Sep; 19(3):195-7. PubMed ID: 1086628 [TBL] [Abstract][Full Text] [Related]
17. "Pure" monosomy 21 pter leads to q21 in a girl born to a couple 46,XX,t(14;21)(p12;q22) and 46,XY,t(5;18)(q32;q22). Rivera H; Rivas F; Plascencia L; Cantú JM Ann Genet; 1983; 26(4):234-7. PubMed ID: 6607704 [TBL] [Abstract][Full Text] [Related]
19. An (11;21) translocation in four generations with chromosome 11 abnormalities in the offspring. A clinical, cytogenetical, and gene marker study. Jacobsen P; Hauge M; Henningsen K; Hobolth N; Mikkelsen M; Philip J Hum Hered; 1973; 23(6):568-85. PubMed ID: 4134631 [No Abstract] [Full Text] [Related]
20. Similar chromosomal abnormalities in several retinoblastomas. Kusnetsova LE; Prigogina EL; Pogosianz HE; Belkina BM Hum Genet; 1982; 61(3):201-4. PubMed ID: 7173862 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]