113 related articles for article (PubMed ID: 1746616)
41. Blepharophimosis and mental retardation (BMR) phenotypes caused by chromosomal rearrangements: description in a boy with partial trisomy 10q and monosomy 4q and review of the literature.
Bartholdi D; Toelle SP; Steiner B; Boltshauser E; Schinzel A; Riegel M
Eur J Med Genet; 2008; 51(2):113-23. PubMed ID: 18262484
[TBL] [Abstract][Full Text] [Related]
42. Characterization of a de novo unbalanced translocation t(14q18q) using microdissection and fluorescence in situ hybridization.
Engelen JJ; Loots WJ; Albrechts JC; Plomp AS; van der Meer SB; Vles JS; Hamers GJ; Geraedts JP
Am J Med Genet; 1998 Feb; 75(4):409-13. PubMed ID: 9482648
[TBL] [Abstract][Full Text] [Related]
43. A case of Alagille's syndrome with translocation (4;14) (q21;q21).
Mujica P; Morali A; Vidailhet M; Pierson M; Gilgenkrantz S
Ann Genet; 1989; 32(2):117-9. PubMed ID: 2757361
[TBL] [Abstract][Full Text] [Related]
44. Translocation (11;13)(q23;q14) as the sole abnormality in a childhood de novo acute myelocytic leukemia.
Tsang KS; Li CK; Lau TT; Wong AP; Leung Y; Ng MH
Cancer Genet Cytogenet; 2004 Apr; 150(1):78-80. PubMed ID: 15041229
[TBL] [Abstract][Full Text] [Related]
45. Additional chromosome in a child as a result of a balanced reciprocal translocation t(12;18)(p13;q12) in his mother's karyotype.
Lassota M; Przełozna B; Płodzien M; Bugno M; Wnuk M; Kotylak Z; Słota E
J Appl Genet; 2005; 46(4):419-21. PubMed ID: 16278518
[TBL] [Abstract][Full Text] [Related]
46. Kallmann syndrome associated with complex chromosome rearrangement.
Casamassima AC; Wilmot PL; Vibert BK; Shapiro LR
Am J Med Genet; 1993 Mar; 45(5):539-41. PubMed ID: 8456820
[TBL] [Abstract][Full Text] [Related]
47. Infant acute lymphoblastic leukemia with t(11;16)(q23;p13.3) and lineage switch into acute monoblastic leukemia.
Stasik C; Ganguly S; Cunningham MT; Hagemeister S; Persons DL
Cancer Genet Cytogenet; 2006 Jul; 168(2):146-9. PubMed ID: 16843104
[TBL] [Abstract][Full Text] [Related]
48. Deletion of chromosome 3 and a 3;20 reciprocal translocation demonstrated by chromosome painting.
Crispino B; Cardoso H; Mimbacas A; Méndez V
Am J Med Genet; 1995 Jan; 55(1):27-9. PubMed ID: 7702091
[TBL] [Abstract][Full Text] [Related]
49. 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]
50. Association between a new 3q;5q chromosomal translocation and dystrophy of human retinal pigment epithelium.
Pereira SR; Silva AS; Bormann EP; Kuppinger O
Genet Mol Res; 2007 Oct; 6(4):1085-90. PubMed ID: 18273801
[TBL] [Abstract][Full Text] [Related]
51. Autosomal dominant congenital cataract associated with chromosomal translocation [t(3;4)(p26.2;p15)].
Reese PD; Tuck-Muller CM; Maumenee IH
Arch Ophthalmol; 1987 Oct; 105(10):1382-4. PubMed ID: 3662912
[TBL] [Abstract][Full Text] [Related]
52. Prenatal diagnosis of de novo X;autosome translocations.
Abrams L; Cotter PD
Clin Genet; 2004 May; 65(5):423-8. PubMed ID: 15099352
[TBL] [Abstract][Full Text] [Related]
53. [Prenatal diagnosis of de novo complex balanced rearrangements in chromosomes 3,4, and 13] ].
Balícek P; Jüttnerová V; Jarosová M; Fialová J; Fiedler Z; Kolmanová J
Cas Lek Cesk; 2001 Mar; 140(4):122-4. PubMed ID: 11284430
[TBL] [Abstract][Full Text] [Related]
54. Balanced nonacrocentric whole-arm reciprocal translocations: a de novo case and literature review.
Farrell SA; Fan YS
Am J Med Genet; 1995 Feb; 55(4):423-6. PubMed ID: 7762581
[TBL] [Abstract][Full Text] [Related]
55. [2 new cases of Y-autosome translocation associated with azoospermia].
Gregori-Romero M; López-Ginés C; Gil R; Galán Sánchez F; Pellín-Pérez A
Rev Clin Esp; 1990 Jun; 187(2):71-3. PubMed ID: 2244061
[TBL] [Abstract][Full Text] [Related]
56. Molecular studies of translocations and trisomy involving chromosome 13.
Robinson WP; Bernasconi F; Dutly F; Lefort G; Romain DR; Binkert F; Schinzel AA
Am J Med Genet; 1996 Jan; 61(2):158-63. PubMed ID: 8669444
[TBL] [Abstract][Full Text] [Related]
57. Pure 4p trisomy due to a de novo 4q;22p dicentric translocated chromosome karyotype 46,XX,-22,+t(4;22)(q1200;p13).
de Almeida JC; Reis DF; Llerena Júnior JC
Ann Genet; 1991; 34(2):108-10. PubMed ID: 1746879
[TBL] [Abstract][Full Text] [Related]
58. Trisomy 15q23----qter due to a de novo t(11;15)(q25;q23) and assignment of the critical segment.
García-Cruz D; García-Esquivel L; Rivera H; Vaca G; Rolón A; Cantú JM
Ann Genet; 1985; 28(3):193-6. PubMed ID: 3879157
[TBL] [Abstract][Full Text] [Related]
59. Autosomal dominant congenital cataract in a Libyan Jewish family: cosegregation with a reciprocal chromosomal translocation [t(3;5)(p22.3; p15.1)].
Zafer E; Meck J; Gerrad L; Pras E; Frydman M; Reish O; Avni I; Pras E
Mol Vis; 2008 Mar; 14():530-2. PubMed ID: 18385787
[TBL] [Abstract][Full Text] [Related]
60. Tuberous sclerosis in a child with de novo translocation t(3;12) (p26.3;q23.3).
Fahsold R; Rott HD; Claussen U; Schmalenberger B
Clin Genet; 1991 Oct; 40(4):326-8. PubMed ID: 1756605
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]