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Journal Abstract Search
559 related items for PubMed ID: 11746010
1. High risk for unbalanced segregation of some reciprocal translocations: a large pedigree containing distal 4q trisomy from t(4;7)(q28;p22). Francisco-Bagnariolli AM, Payão SL, Kawasaki-Oyama RS, Sabbag Filho D, Segato R, de Labio RW, Chauffaille ML, Priest JH. Am J Med Genet; 2001 Nov 01; 103(4):302-7. PubMed ID: 11746010 [Abstract] [Full Text] [Related]
2. Maternal balanced translocation (4;21) leading to an offspring with partial duplication of 4q and 21q without phenotypic manifestations of Down syndrome. El-Ruby M, Hemly NA, Zaki MS. Genet Couns; 2007 Nov 01; 18(2):217-26. PubMed ID: 17710874 [Abstract] [Full Text] [Related]
3. 4p trisomy syndrome: report of 4 additional cases and segregation analysis of 21 families with different translocations. Crane J, Sujansky E, Smith A. Am J Med Genet; 1979 Nov 01; 4(3):219-29. PubMed ID: 517577 [Abstract] [Full Text] [Related]
4. Two sibs with duplication of 4q31-->qter due to 3:1 meiotic disjunction and mild phenotype. Moreira LM, Riegel M. Genet Couns; 2000 Nov 01; 11(3):249-59. PubMed ID: 11043433 [Abstract] [Full Text] [Related]
5. [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 01; 138(11):763-6. PubMed ID: 2290435 [Abstract] [Full Text] [Related]
6. Partial trisomy 18(q11 leads to qter) in an infant and aborted fetus resulting from a balanced paternal translocation t(13;18)(q32:q11). Rosenmann A, Isacson M, Cohen R, Segal M, Cohen MM. Ann Genet; 1978 Mar 01; 21(1):60-4. PubMed ID: 308346 [Abstract] [Full Text] [Related]
7. Unbalanced t(4;11)(q32;q23) in a 34-year-old man with manifestations of distal monosomy 11q and trisomy 4q syndromes. Byatt SA, Baker E, Richards RI, Roberts C, Smith A. Am J Med Genet; 1997 Jun 27; 70(4):357-60. PubMed ID: 9182774 [Abstract] [Full Text] [Related]
8. Trisomy 17p11-pter: unbalanced pericentric inversion, inv(17)(p11q25) in two patients, unbalanced translocations t(4;17)(q27;p11) in a newborn and t(4;17) (p16;p11.2) in a fetus. Lurie IW, Gurevich DB, Binkert F, Schinzel A. Clin Dysmorphol; 1995 Jan 27; 4(1):25-32. PubMed ID: 7735502 [Abstract] [Full Text] [Related]
9. Site-specific reciprocal translocation, t(11;22) (q23;q11), in several unrelated families with 3:1 meiotic disjunction. Zackai EH, Emanuel BS. Am J Med Genet; 1980 Jan 27; 7(4):507-21. PubMed ID: 7211960 [Abstract] [Full Text] [Related]
10. Translocation/duplication of 9p onto a duplicated 4q. Rivera H, Figuera LE, Vasquez AI. Genet Couns; 1992 Jan 27; 3(4):201-3. PubMed ID: 1472355 [Abstract] [Full Text] [Related]
11. Reciprocal chromosome translocations involving short arm of chromosome 9 as a risk factor of unfavorable pregnancy outcomes after meiotic malsegregation 2:2. Panasiuk B, Danik J, Lurie IW, Stasiewicz-Jarocka B, Leśniewicz R, Sawicka A, Kałuzewski B, Midro AT. Adv Med Sci; 2009 Jan 27; 54(2):203-10. PubMed ID: 19758973 [Abstract] [Full Text] [Related]
12. 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 02; 61(1):10-5. PubMed ID: 8741910 [Abstract] [Full Text] [Related]
13. Partial trisomy 4q and monosomy 9p resulting from a familial translocation t(4;9)(q27;p24) in a child with choanal atresia. Wouters CH, van Bodegom TM, Moll HA, Govaerts LC. Ann Genet; 1999 Jan 02; 42(3):160-5. PubMed ID: 10526659 [Abstract] [Full Text] [Related]
14. Partial trisomy of the distal part of 10q: a report of two Egyptian cases. Aglan MS, Kamel AK, Helmy NA. Genet Couns; 2008 Jan 02; 19(2):199-209. PubMed ID: 18618995 [Abstract] [Full Text] [Related]
15. Interchange trisomy 21 by t(1;21)(p22;q22)mat. Dominguez MG, Rivera H, Vasquez AI, Hernández-Zaragoza G, Rivas F. Genet Couns; 2001 Jan 02; 12(4):363-7. PubMed ID: 11837606 [Abstract] [Full Text] [Related]
16. 'Pure' partial trisomy 4q26-->q35.2 resulting from a familial unbalanced translocation t(4;10)(q26;q26.3). Zhang YL, Dai Y, Tu ZG, Li QY. Cytogenet Genome Res; 2009 Jan 02; 127(1):67-72. PubMed ID: 20145385 [Abstract] [Full Text] [Related]
17. Trisomy 20q caused by der(4) t(4;20) (q35;q13.1): report of a new patient and review of the literature. Plotner PL, Smith JL, Northrup H. Am J Med Genet; 2002 Jul 22; 111(1):71-5. PubMed ID: 12124739 [Abstract] [Full Text] [Related]
18. Variable expression of phenotype in offspring with partial monosomy 7q and partial trisomy 8p in a family with a rcp (7;8)(134;p12) translocation. Frints SG, Moerman P, Fryns JP. Genet Couns; 1996 Jul 22; 7(4):313-9. PubMed ID: 8985736 [Abstract] [Full Text] [Related]
19. Identification of a subtle chromosomal translocation in a family with recurrent miscarriages and a child with multiple congenital anomalies. A case report. Shaffer LG, Spikes AS, Macha M, Dunn R. J Reprod Med; 1996 May 22; 41(5):367-71. PubMed ID: 8725766 [Abstract] [Full Text] [Related]
20. A family with segregation of an unbalanced translocation (7;13) (q36;q32) in three patients with severe mental retardation, microcephaly and dysmorphic features, detected by subtelomere FISH: genetic counselling and prenatal diagnosis. Nucaro A, Crisponi G, Minafra L, Rossino R, Cianchetti C. Genet Couns; 2008 May 22; 19(1):37-42. PubMed ID: 18564499 [Abstract] [Full Text] [Related] Page: [Next] [New Search]