183 related articles for article (PubMed ID: 7516625)
21. Prenatal detection and characterization of a small supernumerary marker chromosome (sSMC) derived from chromosome 22 with apparently normal phenotype.
Lin CC; Hsieh YY; Wang CH; Li YC; Hsieh LJ; Lee CC; Tsai CH; Tsai FJ
Prenat Diagn; 2006 Oct; 26(10):898-902. PubMed ID: 16915592
[TBL] [Abstract][Full Text] [Related]
22. De novo concurrent 5p deletion and distal 17q duplication identified by fluorescence in situ hybridization (FISH).
Szego K; Rauer M; Baratta E; Hoo JJ
Ann Genet; 1993; 36(4):224-7. PubMed ID: 8166430
[TBL] [Abstract][Full Text] [Related]
23. [Molecular-cytogenetic identification of partial trisomy of a short arm of chromosome 8].
Zerova-Liubimova TE; Rigel M; Smul'skaia NA; Evseenkova EG; Gorovenko NG; Shintzel A
Tsitol Genet; 2004; 38(4):55-61. PubMed ID: 15715166
[TBL] [Abstract][Full Text] [Related]
24. Partial proximal trisomy 14: identification and molecular characterization in a girl with global developmental delay.
Dutta UR; Pidugu VK; Dalal A
Genet Couns; 2013; 24(2):207-16. PubMed ID: 24032292
[TBL] [Abstract][Full Text] [Related]
25. Meiotic origin of two ring chromosomes 18 in a girl with developmental delay.
Baumer A; Giovannucci Uzielli ML; Guarducci S; Lapi E; Röthlisberger B; Schinzel A
Am J Med Genet; 2002 Nov; 113(1):101-4. PubMed ID: 12400074
[TBL] [Abstract][Full Text] [Related]
26. De novo balanced complex chromosome rearrangement (CCR) involving chromosome 8, 11 and 16 in a boy with mild developmental delay and psychotic disorder.
Goumy C; Mihaescu M; Tchirkov A; Giollant M; Benier C; Francannet C; Jaffray JY; Geneix A; Vago P
Genet Couns; 2006; 17(3):371-9. PubMed ID: 17100206
[TBL] [Abstract][Full Text] [Related]
27. Mosaic normal/15q11-q13 duplication associated with developmental delay but normal phenotype.
Goossens E; Decock P; Potgieter S; Fryns JP
Genet Couns; 1999; 10(2):133-6. PubMed ID: 10422005
[TBL] [Abstract][Full Text] [Related]
28. Cryptic trisomy 5q35.2qter and deletion 1p36.3 characterised using FISH and array-based CGH.
Utine EG; Alanay Y; Aktas D; Alikasifoglu M; Boduroglu K; Vermeesch J; Tuncbilek E; Fryns JP
Eur J Med Genet; 2008; 51(4):343-50. PubMed ID: 18440888
[TBL] [Abstract][Full Text] [Related]
29. Characterization of a complex chromosomal rearrangement in a patient with a typical catlike cry and no other clinical findings of cri-du-chat syndrome.
Sreekantaiah C; Kronn D; Marinescu RC; Goldin B; Overhauser J
Am J Med Genet; 1999 Sep; 86(3):264-8. PubMed ID: 10482877
[TBL] [Abstract][Full Text] [Related]
30. Interstitial duplication 19p.
Stratton RF; DuPont BR; Olsen AS; Fertitta A; Hoyer M; Moore CM
Am J Med Genet; 1995 Jul; 57(4):562-4. PubMed ID: 7573129
[TBL] [Abstract][Full Text] [Related]
31. Cytogenetic and molecular analysis in trisomy 12p.
Allen TL; Brothman AR; Carey JC; Chance PF
Am J Med Genet; 1996 May; 63(1):250-6. PubMed ID: 8723118
[TBL] [Abstract][Full Text] [Related]
32. Prenatal detection of a de novo Yqh-acrocentric translocation.
Ng LK; Kwok YK; Tang LY; Ng PP; Ghosh A; Lau ET; Tang MH
Clin Biochem; 2006 Mar; 39(3):219-23. PubMed ID: 16515778
[TBL] [Abstract][Full Text] [Related]
33. Application of fluorescence in situ hybridization to the identification of different marker chromosomes.
Verschraegen-Spae MR; Quack B; Rousseaux S; Pison H; Messiaen L; De Paepe A; Lespinasse J
Ann Genet; 1998; 41(1):5-10. PubMed ID: 9599644
[TBL] [Abstract][Full Text] [Related]
34. Supernumerary chromosome marker (1) in a developmentally delayed child.
Lanphear N; Lamb A; Oppenheimer S; Soukup S
Am J Med Genet; 1995 Jul; 57(3):400-2. PubMed ID: 7545867
[TBL] [Abstract][Full Text] [Related]
35. Cryptic duplication of the distal segment of 22q due to a translocation (21;22): three case reports and a review of the literature.
Feenstra I; Koolen DA; Van der Pas J; Hamel BC; Mieloo H; Smeets DF; Van Ravenswaaij CM
Eur J Med Genet; 2006; 49(5):384-95. PubMed ID: 16503209
[TBL] [Abstract][Full Text] [Related]
36. Characterization of an inversion duplication of the short arm of chromosome 8 by fluorescent in situ hybridization.
Henderson KG; Dill FJ; Wood S
Am J Med Genet; 1992 Nov; 44(5):615-8. PubMed ID: 1481820
[TBL] [Abstract][Full Text] [Related]
37. Genetic counselling in a prenatal marker chromosome identified as an i (18p) by in situ hybridization.
Darnaude MT; Diaz de Bustamante A; Cabello P; Vallcorba I
Ann Genet; 1996; 39(2):61-3. PubMed ID: 8766134
[TBL] [Abstract][Full Text] [Related]
38. Constitutional tetrasomy 18p.
Bakshi SR; Brahmbhatt MM; Trivedi PJ; Chudoba I
Indian Pediatr; 2006 Apr; 43(4):357-60. PubMed ID: 16651677
[TBL] [Abstract][Full Text] [Related]
39. Spectral karyotyping and fluorescence in situ hybridization analysis of de novo partial trisomy 7p (7p21.2-->pter) and partial monosomy 12q (12q24.33-->qter).
Chen CP; Lin SP; Lin CC; Li YC; Hsieh LJ; Huang JK; Lee CC; Wang W
Genet Couns; 2006; 17(1):57-63. PubMed ID: 16719278
[TBL] [Abstract][Full Text] [Related]
40. Developmental delay, short stature, and minor facial anomalies in a child with ring chromosome 16.
Chodirker BN; Ray M; McAlpine PJ; Riordan D; Vust A; Pugh D; Chudley AE
Am J Med Genet; 1988 Sep; 31(1):145-51. PubMed ID: 2464927
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
