These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
26. [Chromosome rearrangements (balanced translocations) and their importance in perinatal pathology]. Khodzhaeva ZS Akush Ginekol (Mosk); 1981 Jan; (1):9-12. PubMed ID: 7013527 [No Abstract] [Full Text] [Related]
27. Additional chromosome in a child as a result of a balanced reciprocal translocation t(12;18)(p13;q12) in his mother's karyotype. Lassota M; Przełozna B; Płodzien M; Bugno M; Wnuk M; Kotylak Z; Słota E J Appl Genet; 2005; 46(4):419-21. PubMed ID: 16278518 [TBL] [Abstract][Full Text] [Related]
28. De novo balanced translocation: 46, XX, t(13;20)(q34;p 11). Marinescu DD; Cioltei A; Pop T; Ioan D; Maximilian C Endocrinologie; 1978; 16(4):295-8. PubMed ID: 734345 [TBL] [Abstract][Full Text] [Related]
29. Chromosome 6/15 translocation with multiple congenital anomalies. Ming PM; Goodner DM; Park TS Obstet Gynecol; 1977 Feb; 49(2):251-3. PubMed ID: 834413 [TBL] [Abstract][Full Text] [Related]
30. De novo occurrence of 46,XX,t(4;13) (q31;q14) in a mentally retarded girl. Jenkins EC; Curcuru-Giordano FM; Krishna SG; Cantarella J Ann Genet; 1975 Jun; 18(2):117-20. PubMed ID: 1081364 [TBL] [Abstract][Full Text] [Related]
31. [Genetic counseling. Apropos of familial transmission of 21-D translocation]. Attal B; Cottin J; Someily I Bull Fed Soc Gynecol Obstet Lang Fr; 1971; 23(4):494-7. PubMed ID: 5153258 [No Abstract] [Full Text] [Related]
32. Partial trisomy 15 in a male with severe psychomotor retardation (48, XY, + 15q -, + mar(15)). Voss R; Lerer I; Maftzir G; Sheinis M; Cohen MM Am J Med Genet; 1982 Jun; 12(2):131-9. PubMed ID: 7102721 [TBL] [Abstract][Full Text] [Related]
33. Familial translocation with partial trisomy of 13 and 22: evidence that specific regions of chromosomes 13 and 22 are responsible for the phenotype of each trisomy. Kim HJ; Hsu LY; Goldsmith LC; Strauss L; Hirschhorn K J Med Genet; 1977 Apr; 14(2):114-9. PubMed ID: 853317 [TBL] [Abstract][Full Text] [Related]
34. Partial duplication 5q syndrome: phenotypic similarity in two sisters with identical karyotype (partial duplication 5q33 leads to 5qter and partial deficiency 8p23 leads to pter). Bartsch-Sandhoff M; Liersch R Ann Genet; 1977 Dec; 20(4):281-4. PubMed ID: 305758 [TBL] [Abstract][Full Text] [Related]
35. [Translocation t (13:21) (q22:q22) in mother and monosomia 21 and partial trisomy 13 on her son (author's transl)]. Prieto García F; Badía Garrabou L; Ferrer Calvette J An Esp Pediatr; 1977 Dec; 10(12):927-32. PubMed ID: 607844 [TBL] [Abstract][Full Text] [Related]
37. Balanced rearrangement of chromosomes 2, 5, and 13 in a family with duplication 5q and fetal loss. Evans MI; White BJ; Kent SG; Levine MA; Levin SW; Larsen JW Am J Med Genet; 1984 Dec; 19(4):783-90. PubMed ID: 6517101 [TBL] [Abstract][Full Text] [Related]
38. Familial D-D translocation. A family showing transmission through three generations; a case with multiple congenital malformations, and a case of regular 21-trisomic Down's syndrome. Visfeldt J Acta Pathol Microbiol Scand; 1969; 75(4):545-54. PubMed ID: 4246134 [No Abstract] [Full Text] [Related]
39. Cytogenetic findings in 200 children with mental retardation and multiple congenital anomalies of unknown cause. Coco R; Penchaszadeh VB Am J Med Genet; 1982 Jun; 12(2):155-73. PubMed ID: 7102722 [TBL] [Abstract][Full Text] [Related]
40. Isochromosome 21 and other chromosomal abnormalities in a patient with erythroleukaemia. Werner-Favre C; Cabrol C; Beris P; Engel E Ann Genet; 1983; 26(4):240-2. PubMed ID: 6607706 [TBL] [Abstract][Full Text] [Related] [Previous] [Next] [New Search]