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6. E trisomy phenotype associated with small metacentric chromosome and a familial Y-22 translocation. Dumars KW; Fialko G; Larson E Birth Defects Orig Artic Ser; 1976; 12(5):97-104. PubMed ID: 953249 [TBL] [Abstract][Full Text] [Related]
7. Segregation of two independent chromosomal translocations in one family. Miller K; Flatz SD Hum Genet; 1984; 68(1):93-5. PubMed ID: 6500562 [TBL] [Abstract][Full Text] [Related]
8. Inclusion of satellites in an 18/21 translocation chromosome shown by ammonical-silver staining (sat-banding) in case of partial trisomy 18. Neu RL; Ortega CC; Barg GA; Pinto W; Gardner LI; Howell WM; Denton TE J Med Genet; 1976 Dec; 13(6):520-2. PubMed ID: 65472 [TBL] [Abstract][Full Text] [Related]
9. [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]
10. Cytogenetic studies in 12 patients with itai-itai disease. Shiraishi Y Humangenetik; 1975; 27(1):31-44. PubMed ID: 166913 [TBL] [Abstract][Full Text] [Related]
11. Phenotype-karyotype correlations in dup(18q): report of a case and review. Razavi-Encha F; Raoul O; Lescs MC; Danan C Am J Med Genet; 1985 Jul; 21(3):591-5. PubMed ID: 4025391 [TBL] [Abstract][Full Text] [Related]
12. [Do chromosomal abnormalities reappear in subsequent pregnancies and how often?]. Skrzypczak J; Kwinecka-Dmitriew B; Zakrzewska M; Latos-Bieleńska A Ginekol Pol; 2010 Sep; 81(9):681-6. PubMed ID: 20973205 [TBL] [Abstract][Full Text] [Related]
13. [Chromosome aberrations in abortions]. Boué JG; Boué A; Lazar P Ann Genet; 1967 Dec; 10(4):179-87. PubMed ID: 5301690 [No Abstract] [Full Text] [Related]
14. 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]
15. [A familial translocation t(13;17) (q14;q22) diagnosed following the birth of an infant with trisomy 21]. Stoll C; Levy JM; Dorr R; Kapps R J Genet Hum; 1975 Oct; 23 SUPPL():132. PubMed ID: 1214144 [No Abstract] [Full Text] [Related]
17. Trisomy first, translocation second, uniparental disomy and partial trisomy third: a new mechanism for complex chromosomal aneuploidy. Schinzel A; Kotzot D; Brecevic L; Robinson WP; Dutly F; Dauwerse H; Binkert F; Baumer A; Ausserer B Eur J Hum Genet; 1997; 5(5):308-14. PubMed ID: 9412788 [TBL] [Abstract][Full Text] [Related]
18. Frequency of chromosomal aberrations in newborn infants with multiple developmental defects. Chebotarev AN Sov Genet; 1974 Sep; 8(10):1329-30. PubMed ID: 4439048 [No Abstract] [Full Text] [Related]
19. [Chromosomal control of early mammalian development]. Baranov VS Ontogenez; 1983; 14(6):573-89. PubMed ID: 6686316 [TBL] [Abstract][Full Text] [Related]
20. Translocation of 9q/13q resulting in duplication (trisomy 9pter leads to 9q22) and deficiency (monosomy 13pter leads to 13q12). Howard-Peebles PN; Yarbrough KM; Stoddard GR; Rary JM Clin Genet; 1977 Jan; 11(1):46-52. PubMed ID: 830449 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]