344 related articles for article (PubMed ID: 15658621)
21. Partial trisomy of the distal part of 10q: a report of two Egyptian cases.
Aglan MS; Kamel AK; Helmy NA
Genet Couns; 2008; 19(2):199-209. PubMed ID: 18618995
[TBL] [Abstract][Full Text] [Related]
22. Prenatal diagnosis of a fetus with pure partial trisomy 1q32-44 due to a familial balanced rearrangement.
Kímya Y; Yakut T; Egelí U; Ozerkan K
Prenat Diagn; 2002 Nov; 22(11):957-61. PubMed ID: 12424755
[TBL] [Abstract][Full Text] [Related]
23. A case with mosaic partial duplication of 1q: prenatal and postmortem clinical and cytogenetic evaluations.
Karaoguz MY; Biri A; Pala E; Kan D; Poyraz A; Kurdoglu M; Percin EF
Genet Couns; 2006; 17(2):197-204. PubMed ID: 16970038
[TBL] [Abstract][Full Text] [Related]
24. 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; 111(1):71-5. PubMed ID: 12124739
[TBL] [Abstract][Full Text] [Related]
25. Congenital anomalies and developmental delay in a boy with double chromosome 6 derived supernumerary marker.
Oldak M; Waligora J; Gieruszczak-Bialek D; Skorka A; Bocian E; Brycz-Witkowska J; Stankiewicz P; Korniszewski L
Genet Couns; 2006; 17(1):29-34. PubMed ID: 16719274
[TBL] [Abstract][Full Text] [Related]
26. Further delineation of 7p trisomy. Case report and review of literature.
Pallotta R; Dalprà L; Fusilli P; Zuffardi O
Ann Genet; 1996; 39(3):152-8. PubMed ID: 8839888
[TBL] [Abstract][Full Text] [Related]
27. Report of a patient with a trisomy of chromosome region 20q11.2-->20q12 and characterization with FISH.
Wanderley HY; Schrander-Stumpel CT; Visser MO; Van Maanen-Op Het Roodt EA; Loneus WH; Engelen JJ
Genet Couns; 2005; 16(3):277-82. PubMed ID: 16259325
[TBL] [Abstract][Full Text] [Related]
28. 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]
29. 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]
30. Kabuki syndrome and trisomy 10p.
Utine GE; Alanay Y; Atkaş D; Boduroğlu K; Alikaşifoğlu M; Tunçbilek E
Genet Couns; 2008; 19(3):291-300. PubMed ID: 18990985
[TBL] [Abstract][Full Text] [Related]
31. A de novo subtelomeric monosomy 11q (11q24.2-qter) and trisomy 20q (20q13.3-qter) in a girl with findings compatible with Jacobsen syndrome: case report and review.
Courtens W; Wauters J; Wojciechowski M; Reyniers E; Scheers S; van Luijk R; Rooms L; Kooy F; Wuyts W
Clin Dysmorphol; 2007 Oct; 16(4):231-9. PubMed ID: 17786114
[TBL] [Abstract][Full Text] [Related]
32. Further clinical delineation in trisomy 1q32 syndrome.
Nuño-Arana I; González-García JR; García-Cruz D
Ann Genet; 2001; 44(4):175-7. PubMed ID: 11755100
[TBL] [Abstract][Full Text] [Related]
33. Trisomy 1q42 --> qter in a sister and brother: further delineation of the "trisomy 1q42 --> qter syndrome".
Verschuuren-Bemelmans CC; Leegte B; Hodenius TM; Cobben JM
Am J Med Genet; 1995 Jul; 58(1):83-6. PubMed ID: 7573162
[TBL] [Abstract][Full Text] [Related]
34. Monosomy1p36.3 and trisomy 19p13.3 in a child with periventricular nodular heterotopia.
Descartes M; Mikhail FM; Franklin JC; McGrath TM; Bebin M
Pediatr Neurol; 2011 Oct; 45(4):274-8. PubMed ID: 21907895
[TBL] [Abstract][Full Text] [Related]
35. Interstitial 1q43-q43 deletion with left ventricular noncompaction myocardium.
Kanemoto N; Horigome H; Nakayama J; Ichida F; Xing Y; Buonadonna AL; Kanemoto K; Gentile M
Eur J Med Genet; 2006; 49(3):247-53. PubMed ID: 16762826
[TBL] [Abstract][Full Text] [Related]
36. Precocious puberty associated with partial trisomy 18q and monosomy 11q.
Mutesa L; Hellin AC; Jamar M; Pierquin G; Bours V; Verloes A
Genet Couns; 2007; 18(2):201-7. PubMed ID: 17710872
[TBL] [Abstract][Full Text] [Related]
37. Further delineation of deletion 1p36 syndrome in 60 patients: a recognizable phenotype and common cause of developmental delay and mental retardation.
Battaglia A; Hoyme HE; Dallapiccola B; Zackai E; Hudgins L; McDonald-McGinn D; Bahi-Buisson N; Romano C; Williams CA; Brailey LL; Zuberi SM; Carey JC
Pediatrics; 2008 Feb; 121(2):404-10. PubMed ID: 18245432
[TBL] [Abstract][Full Text] [Related]
38. Inv dup del (1)(pter-->q44::q44-->q42:) with the classical phenotype of trisomy 1q42-qter.
De Brasi D; Rossi E; Giglio S; D'Agostino A; Titomanlio L; Farina V; Andria G; Sebastio G
Am J Med Genet; 2001 Nov; 104(2):127-30. PubMed ID: 11746042
[TBL] [Abstract][Full Text] [Related]
39. Borderline intelligence and discrete craniofacial dysmorphism in an adolescent female with partial trisomy 7p due to a de novo tandem duplication 7 (p15.1-->p21.3).
Kleczkowska A; Decock P; van den Berghe H; Fryns JP
Genet Couns; 1994; 5(4):393-7. PubMed ID: 7888144
[No Abstract] [Full Text] [Related]
40. Partial trisomy 13 in an infant with a mild phenotype: application of fluorescence in situ hybridization in cytogenetic syndromes.
Begovic D; Hitrec V; Lasan R; Letica L; Baric I; Sarnavka V; Galic S
Croat Med J; 1998 Jun; 39(2):212-5. PubMed ID: 9575279
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
