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.
401 related articles for article (PubMed ID: 7856655)
21. 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]
22. Molecular and cytogenetic characterization of 9p- abnormalities. Teebi AS; Gibson L; McGrath J; Meyn MS; Breg WR; Yang-Feng TL Am J Med Genet; 1993 May; 46(3):288-92. PubMed ID: 8488873 [TBL] [Abstract][Full Text] [Related]
23. Cytogenetic abnormalities in hepatoblastoma: report of two new cases and review of the literature suggesting imbalance of chromosomal regions on chromosomes 1, 4, and 12. Nagata T; Nakamura M; Shichino H; Chin M; Sugito K; Ikeda T; Koshinaga T; Fukuzawa M; Inoue M; Mugishima H Cancer Genet Cytogenet; 2005 Jan; 156(1):8-13. PubMed ID: 15588850 [TBL] [Abstract][Full Text] [Related]
24. 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]
25. 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]
26. Segregation of a paternal insertional translocation results in partial 4q monosomy or 4q trisomy in two siblings. Hegmann KM; Spikes AS; Orr-Urtreger A; Shaffer LG Am J Med Genet; 1996 Jan; 61(1):10-5. PubMed ID: 8741910 [TBL] [Abstract][Full Text] [Related]
27. Tandem dup (1p) within the short arm of chromosome 1 in a child with ambiguous genitalia and multiple congenital anomalies. Elejalde BR; Opitz JM; de Elejalde MM; Gilbert EF; Abellera M; Meisner L; Lebel RR; Hartigan JM Am J Med Genet; 1984 Apr; 17(4):723-30. PubMed ID: 6539070 [TBL] [Abstract][Full Text] [Related]
28. Trisomy of 8q22.3 approximately q23-qter following an unbalanced 1;8 translocation in a boy with multiple anomalies. Ergun MA; Balci S; Konaç E; Kan D; Menevşe S; Bartsch O Turk J Pediatr; 2004; 46(4):384-7. PubMed ID: 15641279 [TBL] [Abstract][Full Text] [Related]
29. A patient with an interstitial duplication of chromosome 5p11-p13.3 further confirming a critical region for 5p duplication syndrome. Loscalzo ML; Becker TA; Sutcliffe M Eur J Med Genet; 2008; 51(1):54-60. PubMed ID: 18006398 [TBL] [Abstract][Full Text] [Related]
30. Virilization of the external genitalia and severe mental retardation in a girl with an unbalanced translocation 1;18. de Pater JM; Poot M; Beemer FA; Bijlsma JB; Hack WW; Van Dam WM; Eleveld MJ; Loneus WH; Engelen JJ Eur J Med Genet; 2006; 49(1):19-27. PubMed ID: 16473306 [TBL] [Abstract][Full Text] [Related]
31. De novo complex chromosome rearrangement: a study of two patients. Melo DG; Huber J; Giuliani LR; Mazzucatto LF; Riegel M; Pina-Neto JM Genet Couns; 2004; 15(3):303-10. PubMed ID: 15517822 [TBL] [Abstract][Full Text] [Related]
32. The dup(3)(p25 leads to pter) syndrome: a case with holoprosencephaly. Martin NJ; Steinberg BG Am J Med Genet; 1983 Apr; 14(4):767-72. PubMed ID: 6846406 [TBL] [Abstract][Full Text] [Related]
33. A dysmorphic newborn infant with a complex rearrangement involving chromosomes 2, 4, and 6 detected by fluorescence in situ hybridization (FISH). Hoffman DJ; Punnett HH; Pyeritz RE Am J Perinatol; 2004 Feb; 21(2):69-71. PubMed ID: 15017469 [TBL] [Abstract][Full Text] [Related]
34. Apparent CHARGE association and chromosome anomaly: chance or contiguous gene syndrome. Clementi M; Tenconi R; Turolla L; Silvan C; Bortotto L; Artifoni L Am J Med Genet; 1991 Nov; 41(2):246-50. PubMed ID: 1785643 [TBL] [Abstract][Full Text] [Related]
35. Duplication 7p de novo and literature review. Zerres K; Schwanitz G; Gellissen K; Schroers L; Sohler R Ann Genet; 1989; 32(4):225-9. PubMed ID: 2692511 [TBL] [Abstract][Full Text] [Related]
36. De novo partial 2p duplication with postmortem description. Monteleone PL; Blair JD; Graviss ER; Chen SC; Salvador A; Grzegocki JA; Monteleone JA Am J Med Genet; 1981; 10(1):55-64. PubMed ID: 7197468 [TBL] [Abstract][Full Text] [Related]
37. Two sibs with different phenotypes due to adjacent-1 segregation of a subtle translocation t(4;5)(p16.3;p15.3)mat. Qumsiyeh MB; Stevens CA Am J Med Genet; 1993 Sep; 47(3):387-91. PubMed ID: 8135287 [TBL] [Abstract][Full Text] [Related]
38. De novo tandem duplication of the middle segment of the long arm of chromosome 14. Ito M; Mutoh K; Okuno T; Mikawa H; Edagawa J; Abe T Ann Genet; 1983; 26(2):116-9. PubMed ID: 6604486 [TBL] [Abstract][Full Text] [Related]
39. Familial partial duplication (1)(p21p31). Hoechstetter L; Soukup S; Schorry EK Am J Med Genet; 1995 Nov; 59(3):291-4. PubMed ID: 8599351 [TBL] [Abstract][Full Text] [Related]
40. [Translocation trisomy 4q in 2 siblings as a sequela of paternal balanced reciprocal translocation: t(1;4)(q44;q31)]. Bode H; Bühler EM; Wyler F; Hadzilselimovic F Monatsschr Kinderheilkd; 1990 Nov; 138(11):763-6. PubMed ID: 2290435 [TBL] [Abstract][Full Text] [Related] [Previous] [Next] [New Search]