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22. [Identification of 2 familial translocations]. Laurent C; Biemont MC; Robert JM; Dutrillaux B Ann Genet; 1974 Dec; 17(4):279-81. PubMed ID: 4548825 [No Abstract] [Full Text] [Related]
23. Familial cases of marker chromosomes of groups 21-22 and 13-15 (Gpss and Dp+). Kyaosaar ME Sov Genet; 1973 Nov; 7(7):913-8. PubMed ID: 4777944 [No Abstract] [Full Text] [Related]
29. [A study of the offspring of t(21q Dq) translocation carriers]. Dutrillaux B; Lejeune J Ann Genet; 1969 Jun; 12(2):77-82. PubMed ID: 4243780 [No Abstract] [Full Text] [Related]
30. A de novo translocation, 14q21q, with a microchromosome-14p21p. Abeliovich D; Katz M; Karplus M; Carmi R Am J Med Genet; 1985 Sep; 22(1):29-33. PubMed ID: 2931981 [TBL] [Abstract][Full Text] [Related]
31. Identification of a familial Robertsonian translocation t(13q14q) by means of thermic moderated denaturation. Stoll C; Levy JM Humangenetik; 1973 Jul; 19(2):211-4. PubMed ID: 4744407 [No Abstract] [Full Text] [Related]
32. Patterns of D chromosome involvement in human (DqDq) and (DqGq) Robertsonian rearrangements. Hecht F; Kimberling WJ Am J Hum Genet; 1971 Jul; 23(4):361-7. PubMed ID: 5097902 [No Abstract] [Full Text] [Related]
33. Relationship between anomalies of phenotype and karyotype in human embryogenesis. Kuliev AM Sov Genet; 1974 Jul; 8(7):910-20. PubMed ID: 4424716 [No Abstract] [Full Text] [Related]
34. [T (14q-; 21q + ) translocation in the father. Partial trisomy 14 and monosomy 21 in the daughter]. Laurent C; Dutrillaux B; Biemont MC; Genoud J; Bethenod M Ann Genet; 1973 Dec; 16(4):281-4. PubMed ID: 4544094 [No Abstract] [Full Text] [Related]
36. A peculiar t(21 ; 14) translocation, associated with a pericentric inversion of the Y chromosome in a mongol boy. Orye E; Verhaaren H Ann Genet; 1974 Sep; 17(3):217-20. PubMed ID: 4141590 [No Abstract] [Full Text] [Related]
37. Trisomy and D/G translocation mongolism in brothers. Ingalls TH; Henry TA N Engl J Med; 1968 Jan; 278(1):10-4. PubMed ID: 4229204 [No Abstract] [Full Text] [Related]