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23. Chromosome abnormalities in South African mental retardates. Ally FE; Grace HJ S Afr Med J; 1979 Apr; 55(18):710-2. PubMed ID: 156963 [TBL] [Abstract][Full Text] [Related]
24. Identification of supernumerary marker chromosomes derived from chromosomes 5, 6, 19, and 20 using FISH. Stankiewicz P; Bocian E; Jakubów-Durska K; Obersztyn E; Lato E; Starke H; Mroczek K; Mazurczak T J Med Genet; 2000 Feb; 37(2):114-20. PubMed ID: 10662811 [TBL] [Abstract][Full Text] [Related]
25. Molecular cytogenetic study of supernumerary marker chromosomes in an unselected group of children. Gravholt CH; Friedrich U Am J Med Genet; 1995 Mar; 56(1):106-11. PubMed ID: 7747772 [TBL] [Abstract][Full Text] [Related]
26. [Value of silver staining technics for the study of acrocentric ring chromosomes and supernumerary microchromosomes]. Teyssier M; Moreau N C R Seances Soc Biol Fil; 1984; 178(3):251-6. PubMed ID: 6208982 [TBL] [Abstract][Full Text] [Related]
27. Possible origin of a small bisatellited additional chromosome. Bartsch HD; de Azevedo Moreira LM; Röhrborn G; Claussen U; Gebauer HJ Hum Genet; 1980; 54(3):319-22. PubMed ID: 6931099 [TBL] [Abstract][Full Text] [Related]
28. A case of D13 ring chromosome. Cossu P; Diana G; Mameli M; Cardia S; Milia A; Floris G; Cao A Hum Genet; 1979 Jan; 46(1):111-4. PubMed ID: 429001 [TBL] [Abstract][Full Text] [Related]
29. Prophase analysis of ring chromosome 13--an attempt at phenotype-karyotype correlation. Lagergren M; Börjeson M; Mitelman F Hereditas; 1980; 93(2):231-3. PubMed ID: 7440241 [No Abstract] [Full Text] [Related]
30. [Genetic determination of the activity of nucleolar-organizing regions of human chromosomes]. Egolina NA; Davudov AZ; Beniush VA; Zakharov AF Biull Eksp Biol Med; 1981 Mar; 91(3):350-3. PubMed ID: 7195749 [TBL] [Abstract][Full Text] [Related]
31. Cytogenetic study of individuals suspected of chromosome anomalies. Singh DN Clin Pediatr (Phila); 1977 Jul; 16(7):619-22. PubMed ID: 862299 [No Abstract] [Full Text] [Related]
32. Supernumary marker chromosomes in a mentally retarded population identified as inv dup(15). Kirkilionis AJ; Sergovich FR Clin Genet; 1987 Jun; 31(6):425-8. PubMed ID: 3621648 [TBL] [Abstract][Full Text] [Related]
33. A cytogenetic survey of an institution for the mentally retarded: I. Chromosome abnormalities. Jacobs PA; Matsuura JS; Mayer M; Newlands IM Clin Genet; 1978 Jan; 13(1):37-60. PubMed ID: 146575 [TBL] [Abstract][Full Text] [Related]
34. Is it always the same NOR that is more active in a pair of acrocentrics with distinct AG-stainings? Jotterand-Bellomo M; van Melle G Hum Genet; 1981; 59(2):185. PubMed ID: 6173302 [No Abstract] [Full Text] [Related]
35. A reassessment of the karyotype of Papio ursinus. Homoeology between human chromosome 15 and 22 and a characteristic submetacentric baboon chromosome. Bernstein R; Pinto M; Morcom G; Bielert C Cytogenet Cell Genet; 1980; 28(1-2):55-63. PubMed ID: 7449436 [TBL] [Abstract][Full Text] [Related]
36. Satellite associations and silver staining in a case of multiple G and D variants. Di Lernia R; Riva ML; Dalprà L; Ginelli E Hum Genet; 1980 Feb; 53(2):237-40. PubMed ID: 6928412 [TBL] [Abstract][Full Text] [Related]
37. A note on a patient with a ring-22 chromosome identified by banding. Stewart A; Richards BW J Ment Defic Res; 1976 Jun; 20(2):95-8. PubMed ID: 940150 [No Abstract] [Full Text] [Related]
38. X;15 translocation in a retarded girl: X inactivation pattern and attempt to localise the hexosaminidase A and other loci. Bernstein R; Dawson B; Kohl R; Jenkins T J Med Genet; 1979 Aug; 16(4):254-62. PubMed ID: 290816 [TBL] [Abstract][Full Text] [Related]
39. A familial F/G translocation [t(p-; 22q+)] observed in three generations. Cohen MM; Davidson RG; Brown JA Clin Genet; 1975 Feb; 7(2):120-7. PubMed ID: 1132159 [TBL] [Abstract][Full Text] [Related]
40. Chromosomes as markers in human cancer. Sandberg AA Int Adv Surg Oncol; 1981; 4():311-36. PubMed ID: 7019095 [No Abstract] [Full Text] [Related] [Previous] [Next] [New Search]