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43. Trisomy 3q2 and Pierre-Robin sequence in a boy with unbalanced 46,XY, der(10), t(3;10)(q23;q26.3) de novo karyotype. Kleczkowska A; Fryns JP; Moerman F; Martens M; Eggermont E; Jaeken J; Van den Berghe H Helv Paediatr Acta; 1988 Nov; 43(3):245-8. PubMed ID: 3220792 [TBL] [Abstract][Full Text] [Related]
44. Application of new staining techniques to the study of human chromosomes. Miller OJ; Miller DA; Warburton D Prog Med Genet; 1973; 9():1-47. PubMed ID: 4123248 [No Abstract] [Full Text] [Related]
45. Noninactivation of a portion of Xq28 in a balanced X-autosome translocation. Du Sart D; Kalitsis P; Schmidt M Am J Med Genet; 1992 Jan; 42(2):156-60. PubMed ID: 1733163 [TBL] [Abstract][Full Text] [Related]
46. Use of fluorescence in situ hybridization to clarify a complex chromosomal rearrangement in a child with multiple congenital anomalies. Spikes AS; Hegmann K; Smith JL; Shaffer LG Am J Med Genet; 1995 May; 57(1):31-4. PubMed ID: 7645595 [TBL] [Abstract][Full Text] [Related]
47. Some ideas on the time sequence of chromosome function in human organogenesis. Lur'e IV Sov Genet; 1974 Jul; 8(6):774-6. PubMed ID: 4417132 [No Abstract] [Full Text] [Related]
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51. [The human genome with special emphasis on chromosome 1]. KamarĂ½t J Cas Lek Cesk; 1995 Jan; 134(1):24-9. PubMed ID: 7712520 [TBL] [Abstract][Full Text] [Related]
58. Report of the second international workshop on human chromosome 10 mapping 1997. Meitinger T; Scharfe C; Call K; Moschonas N Cytogenet Cell Genet; 1997; 78(3-4):184-94. PubMed ID: 9465886 [No Abstract] [Full Text] [Related]
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